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N-甲氧基甲基-N-(三甲基硅烷)苄基胺 | 93102-05-7

N-甲氧基甲基-N-(三甲基硅烷)苄基胺
benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
93102-05-7
C13H23NOSi
237.413324594498
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:N-甲氧基甲基-N-(三甲基硅烷)苄基胺结构式
24866346
名称和标识符
MDL MFCD00674005
InChIKey RPZAAFUKDPKTKP-UHFFFAOYSA-N
Inchi 1S/C13H23NOSi/c1-15-11-14(12-16(2,3)4)10-13-8-6-5-7-9-13/h5-9H,10-12H2,1-4H3
SMILES [Si](C)(C)(C)CN(COC)CC1C=CC=CC=1
BRN 4311216
别名信息
- 中文别名 -
  • N-甲氧基甲基-N-(三甲基硅烷)苄基胺
  • N-(甲氧甲基)-N-(三甲基硅甲基)苄胺
  • N-甲氧基甲基-N-(三甲基硅烷甲基)苄胺
  • N-苄基-N-(甲氧甲基)-N-三甲基硅基甲胺
  • N-(甲氧基甲基)-N-(三甲基硅基甲基)苄胺
  • N-(甲氧基甲基)-N-(三甲基硅甲基)苄胺
  • N-(甲氧甲基)-N-(三甲基硅基甲)苄胺
  • N-(甲氧甲基)-N-(三甲基硅甲基)
  • N-(甲氧甲基)-N-(三甲基硅甲基)苄胺,N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
  • N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine N-苄基-N-(甲氧甲基)-N-三甲基硅基甲胺
  • N-甲氧基甲基-N-(三甲基硅烷甲基)苄基胺
  • N-甲氧基甲基-N-三甲基硅甲基苄胺(B12)
  • N-苄基-N-甲氧甲基-N-(三甲基硅基)甲胺
- 英文别名 -
  • N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
  • N-Benzyl-N-(methoxymethyl)-N-trimethylsilylmethylamine
  • Benzenemethanamine, N-(methoxymethyl)-N-[(trimethylsilyl)methyl]-
  • Benzyl-methoxymethyl-trimethylsilanylmethyl-amine
  • N-(methoxymethyl)-1-phenyl-N-(trimethylsilylmethyl)methanamine
  • N-(Methoxymethyl)-N-
  • N-(Methoxymethyl)-N-(trimethylsilylmethyl)-benzylamine
  • N-(Methoxymethyl)-N-[(trimethylsilyl-methyl]-benzylamine
  • N-Benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine
  • N-Benzyl-N-(methoxymethyl)trimethylsilylmethylamine
  • benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
  • n-methoxymethyl-n-(trimethylsilylmethyl)benzylamine
  • N-Benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methanamine
  • Benzen
  • N-(Methoxymethyl)-N-[(trimethylsilyl)methyl]benzenemethanamine (ACI)
  • (Benzyl)(methoxymethyl)(trimethylsilanylmethyl)amine
  • (Benzyl)(methoxymethyl)-N-[(trimethylsilyl)methyl]amine
  • [(Methyloxy)methyl](phenylmethyl)[(trimethylsilyl)methyl]amine
  • [(N-Benzyl-N-methoxymethylamino)methyl]trimethylsilane
  • Benzyl(methoxymethyl)[(trimethylsilyl)methyl]amine
  • N-(Methoxymethyl)(phenyl)-N-[(trimethylsilyl)methyl]methanamine
  • N-(Methoxymethyl)-1-phenyl-N-(trimethylsilylmethyl)methanamine
  • N-(Methoxymethyl)-N-(phenylmethyl)-N-[(trimethylsilyl)methyl]amine
  • N-(Methoxymethyl)-N-(trimethylsilylmethyl)-N-benzylamine
  • N-Benzyl-N-methoxymethyl-N-[(trimethylsilyl)methyl]amine
  • NSC 601818
  • N-(methoxymethyl)-N-(phenylmethyl)-N-(trimethylsilyl)methyl amine
  • N-(methoxymethyl)-N-(phenylmethyl)-N-(trimethylsilyl)methylamine
  • n-(methoxymethyl)(phenyl)-n-((trimethylsilyl) methyl)methanamine
  • N-benzyl-N-(methoxymethyl)tri-methylsilylmethylamine
  • [(methyloxy)methyl](phenylmethyl)[(trimethylsilyl)methyl]amine
  • N-benzyl-N-(methoxymethyl)-N-trimethylsilylmethyl amine
  • BP-12704
  • N-(methoxymethyl)-N-(trimethylsilylmethyl)benzyl-amine
  • N-benzyl-N(methoxymethyl)-N-trimethylsilylmethylamine
  • N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methan-amine
  • 93102-05-7
  • N-(methoxymethyl)-N-(phenylmethyl)-N-(trimethylsilyl) methylamine
  • N-(Methoxymethyl)-N-[(Trimethylsilyl)Methyl]Benzenemethanamine(>90%)
  • N-methoxymethyl-N-(phenylmethyl)tri-methylsilylmethylamine
  • n-benzyl-1-methoxy-n-((trimethylsilyl)methyl)-methanamine
  • N-benzyl(methoxy)-N-((trimethylsilyl)methyl)methanamine
  • N-(methoxymethyl)-N-(trimethylsilylmethyl) benzylamine
  • N-benzyl-N(methoxymethyl)trimethylsilylmethylamine
  • AM87445
  • NSC-601818
  • PB24674
  • N-benzyl-1-methoxy-N-((trimethylsilyl)-methyl)methanamine
  • N-BENZYL-N-(METHOXYMETHYL)TRIMETHYLSILYLMETHYLAMINE
  • F0001-2246
  • n-benzyl-1-methoxy-n-[(trimethylsilyl) methyl]methanamine
  • N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine
  • GS-3053
  • benzyl-methoxymethyltrimethylsilanylmethylamine
  • A21270
  • N-benzyl-N-(methoxymethyl) trimethylsilylmethylamine
  • MFCD00674005
  • N-benzyl-1-methoxy-N-[(trimethylsilyl)methyl)methanamine
  • BB 0263001
  • EN300-54483
  • N-(methoxylmethyl)-N-(trimethylsilylmethyl)-benzylamine
  • N-benzyl-N-(methoxymethyl)trimethylsilylmethyl-amine
  • N-benzyl-N-methoxymethyl-N-trimethylsilylmethylamine
  • A905491
  • DTXSID30326563
  • benzyl(methoxymethyl)-trimethylsilylmethylamine
  • N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, 96%
  • N-(Methoxymethyl)-N-[(trimethylsilyl)methyl]benzenemethanamine (>90%)
  • N-(METHOXYMETHYL)-N-[(TRIMETHYLSILYL)METHYL]-BENZENEMETHANAMINE
  • CS-0010304
  • N-(METHOXYMETHYL)-N-((TRIMETHYLSILYL)METHYL)(PHENYL)METHANAMINE
  • N-Methoxymethyl-N-(Trimethylsilylmethyl)Benzylamine, 94%
  • N-methoxymethyl-N-trimethylsilylmethyl benzyl amine
  • N-benzyl-N-methoxymethyl-N-(tri-methylsilylmethyl)-amine
  • benzyl(methoxymethyl)trimethylsilanylmethylamine
  • N(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine
  • benzyl methoxymethyl trimethylsilylmethyl amine
  • SY001990
  • N-benzyl-N-(methoxymethyl)-N-[(trimethylsilyl)methyl]amine
  • AKOS009156524
  • J-800249
  • N-benzyl-N-methoxymethyl-N-(trimethylsilylmethyl)amine
  • n-methoxymethyl-n-trimethylsilylmethylbenzyl amine
  • BCP27203
  • N-benzyl-N-methoxymethyl-N-(trimethylsilyl)methylamine
  • S00978
  • Benzyl(methoxymethyl)trimethylsilylmethylamine
  • N-benzyl-N-(methoxymethyl)-trimethylsilylmethylamine
  • N-(Methoxymethyl)-N-(trimethylsilylmethyl)benzylamine, tech grade
  • n-benzyl-1-methoxy-n-[(trimethylsilyl)-methyl]methanamine
  • NSC601818
  • N-Benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methylamine
  • B1938
  • N-Methoxymethyl-N-trimethylsilylmethylbenzylamine
  • N-(methoxylmethyl)-N-(trimethylsilylmethyl)benzylamine
  • N-benzyl-N-methoxymethyl-N-(trimethylsilylmethyl)-amine
  • N-benzyl-1-methoxy-N-(trimethylsilylmethyl)methanamine
  • SCHEMBL102928
  • LB-0211
  • N-methoxymethyl-N-(phenylmethyl)trimethylsilylmethylamine
  • N-(methoxymethyl)(phenyl)-N-((trimethylsilyl)methyl)methanamine
  • FT-0649644
  • J-640250
  • N-benzyl -1-methoxy-N-[(trimethylsilyl)methyl]methanamine
  • C13H23NOSi
  • N-methoxymethyl-N-trimethylsilylmethyl-benzylamine
  • N-benzyl-N-(methoxymethyl)-N-(trimethylsilylmethyl)amine
  • AC-5090
  • RPZAAFUKDPKTKP-UHFFFAOYSA-N
  • N-benzyl-N-(methoxymethyl)trimethyl-silylmethylamine
物化性质
实验特性
LogP 3.38820
PSA 12.47000
折射率 n20/D 1.492(lit.)
沸点 78°C/0.6mmHg(lit.)
闪点 华氏:150.8 °F
摄氏:66 °C
溶解度 Soluble in chloroform, ethyl acetate.
颜色与性状 液体
溶解性 未确定
敏感性 Moisture & Light Sensitive
密度 0.928 g/mL at 25 °C(lit.)
计算特性
精确分子量 237.15500
氢键供体数量 0
氢键受体数量 2
可旋转化学键数量 6
同位素质量 237.155
重原子数量 16
复杂度 185
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP)
互变异构体数量
表面电荷 0
拓扑分子极性表面积 12.5
国际标准相关数据
EINECS 24866346
海关数据
海关编码 2931900090
海关数据

中国海关编码:

2931900090

概述:

2931900090. 其他有机-无机化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:AB(入境货物通关单,出境货物通关单). 最惠国关税:6.5%. 普通关税:30.0%

Summary:

2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
Synthesis of novel 4-substituted imidazolidines
Gao, Bin-heng; Chen, Ken; Xu, Liang, Hecheng Huaxue, 2011, 19(3), 291-294

合成路线:1 步

反应条件:
参考文献:
A Practical Large-Scale Synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol via Asymmetric 1,3-Dipolar Cycloaddition
Kotian, Pravin L.; Lin, Tsu-Hsing; El-Kattan, Yahya; Chand, Pooran, Organic Process Research & Development, 2005, 9(2), 193-197

合成路线:1 步

反应条件:
参考文献:
Discovery of the PARP (poly ADP-ribose polymerase) inhibitor 2-(1-(4,4-difluorocyclohexyl)piperidin-4-yl)-1H-benzo[d]imidazole-4-carboxamide for the treatment of cancer
Tang, Lin; Wu, Weibin; Zhang, Cunlong; Shi, Zhichao; Chen, Dawei; et al, Bioorganic Chemistry, 2021, 114,

合成路线:1 步

反应条件:
参考文献:
Fluorine-containing substituted benzimidazole derivatives and their application in preparing drugs for prevention and treatment of PARP (poly (ADP-ribose) polymerase)-related diseases
, World Intellectual Property Organization, , ,

合成路线:1 步

反应条件:
参考文献:
Bronsted Acid or Lewis Acid Catalyzed [3+3] Cycloaddition of Azomethine Imines with N-Benzyl Azomethine Ylide: A Facile Access to Bicyclic N-Heterocycles
Li, Shuo-ning; Yu, Bin; Liu, Jia; Li, Hong-lian; Na, Risong, Synlett, 2016, 27(2), 282-286

合成路线:1 步

反应条件:
参考文献:
Discovery of 2-(1-(3-(4-chloroxyphenyl)-3-oxo- propyl)pyrrolidine-3-yl)-1H-benzo[d]imidazole-4-carboxamide: a potent poly(ADP-ribose) polymerase (PARP) inhibitor for treatment of cancer
Min, Rui ; Wu, Weibin; Wang, Mingzhong; Tang, Lin; Chen, Dawei; et al, Molecules, 2019, 24(10),

合成路线:1 步

反应条件:
参考文献:
Preparation of pyrazolo[4,3-d]pyrimidin-7(6H)-one derivatives as PDE9 inhibitors
, World Intellectual Property Organization, , ,

合成路线:1 步

反应条件:
参考文献:
Oxazole compound with antifungal activity and preparation method
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Preparation of heterocyclyl-substituted diazabicyclooctanes having selective 5-HT1Dα antagonist activity
, World Intellectual Property Organization, , ,

合成路线:1 步

参考文献:
Chemistry of organosilicon compounds. 195. N-(Trimethylsilylmethyl)aminomethyl ethers as azomethine ylide synthons. A new and convenient access to pyrrolidine derivatives
Hosomi, Akira; Sakata, Yasuyuki; Sakurai, Hideki, Chemistry Letters, 1984, (7), 1117-20

合成路线:1 步

反应条件:
参考文献:
Use of N-[(trimethylsilyl)methyl]amino ethers as capped azomethine ylide equivalents
Padwa, Albert; Dent, William, Journal of Organic Chemistry, 1987, 52(2), 235-44

合成路线:1 步

反应条件:
参考文献:
Preparation of 1,2,3,3a,8,8a-hexahydro-2,7a-diazacyclopenta[a]inden-7-ones and related compounds as nicotinic acetylcholine receptor ligands useful in modulating cholinergic function and in the treatment of addictive disorders
, World Intellectual Property Organization, , ,

合成路线:1 步

反应条件:
参考文献:
Design, synthesis, and validation of a β-turn mimetic library targeting protein-protein and peptide-receptor interactions
Whitby, Landon R.; Ando, Yoshio; Setola, Vincent; Vogt, Peter K.; Roth, Bryan L.; et al, Journal of the American Chemical Society, 2011, 133(26), 10184-10194

合成路线:1 步

反应条件:
参考文献:
Synthesis of methyl pyrrolidine-3-carboxylate
Xie, Honglei; Jia, Yunhong; Cai, Dong, Huaxue Tongbao, 2011, 74(9), 850-852

合成路线:1 步

反应条件:
参考文献:
Small molecule inhibitors of Myc/Max dimerization and Myc-induced cell transformation
Shi, Jin; Stover, James S.; Whitby, Landon R.; Vogt, Peter K.; Boger, Dale L., Bioorganic & Medicinal Chemistry Letters, 2009, 19(21), 6038-6041

合成路线:1 步

反应条件:
参考文献:
Stereo-, Regio-, and Chemoselective [3 + 2]-Cycloaddition of (2E,4E)-Ethyl 5-(Phenylsulfonyl)penta-2,4-dienoate with Various Azomethine Ylides, Nitrones, and Nitrile Oxides: Synthesis of Pyrrolidine, Isoxazolidine, and Isoxazoline Derivatives and a Computational Study
Sankar, Ulaganathan; Surya Kumar, Ch. Venkata; Subramanian, V.; Balasubramanian, K. K.; Mahalakshimi, S., Journal of Organic Chemistry, 2016, 81(6), 2340-2354

合成路线:1 步

反应条件:
参考文献:
Improved process for production of N-methoxymethyl trimethylsilylmethylamines by base-catalyzed methoxymethylation with paraformaldehyde in methanol
, Germany, , ,

合成路线:1 步

反应条件:
参考文献:
Process for preparation of chiral 4-(hydroxymethyl)pyrrolidin-3-ols
, United States, , ,

合成路线:1 步

反应条件:
参考文献:
Method for synthesizing N-methoxymethyl-N-(trimethylsilylmethyl)benzylamine
, China, , ,
专业数据库参考
PubChemId 24866346
参考资料
Reaxys RN 4311216
Beilstein MFCD00674005
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