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2,3-二羟基萘 | 92-44-4

2,3-二羟基萘
2,3-Dihydroxynaphthalene
92-44-4
C10H8O2
160.169322967529
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:2,3-二羟基萘结构式
7091
2,3-二羟基萘价格
名称和标识符
MDL MFCD00004073
InChIKey JRNGUTKWMSBIBF-UHFFFAOYSA-N
Inchi 1S/C10H8O2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,11-12H
SMILES OC1C(O)=CC2C(=CC=CC=2)C=1
BRN 0742375
别名信息
- 中文别名 -
  • 2,3-二羟基萘
  • 2,3-萘二酚
  • 2,3-Dihydroxynaphthalene 2,3-萘二酚
  • 2,3-二羟基萘 2,3-萘二酚
  • 2,3-二羟基萘(2,3-萘二酚)
  • 2,3-萘二醇
  • 3-硝基-4-羟基-7-氯喹啉
  • 2,3-二萘酚
- 英文别名 -
  • Naphthalene-2,3-diol
  • 2,3-Naphthalenediol
  • 2,3-Dihydroxynaphthalene
  • 2,3-Dihydroxynapthalene
  • 2,3-Dihydroxy naphthalene
  • 2,3-Dihydroxynaphthlene
  • Naphthalenediol-(2,3)
  • JRNGUTKWMSBIBF-UHFFFAOYSA-N
  • 2,3-DIHYDROXY-NAPHTHALENE
  • O9U131030Z
  • 3-hydroxy-2-naphthol
  • 2-Hydroxy-3-naphthol
  • 2,3dihydroxynaphthalene
  • DSSTox_CID_23903
  • WLN: L66J CQ DQ
  • DSSTox_GSID_43903
  • KSC4
  • D 0593
  • NSC 8707
  • 2,3-Dihydroxynaphthalene,98%
物化性质
实验特性
LogP 2.25100
PSA 40.46000
折射率 1.5178 (estimate)
水溶性 微溶
沸点 353.9 ℃ at 760 mmHg
熔点 161-165 °C (lit.)
162-164 °C
闪点 175 ºC
溶解度 4g/l
颜色与性状  叶状结晶。
PH值 6 (1g/l, H2O, 20℃)
溶解性 溶于热水。
敏感性 对空气敏感
密度 1.0924 (rough estimate)
计算特性
精确分子量 160.05200
氢键供体数量 2
氢键受体数量 2
可旋转化学键数量 0
重原子数量 12
复杂度 140
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) 2.5
互变异构体数量 4
表面电荷 0
拓扑分子极性表面积 40.5
国际标准相关数据
EINECS 8707
海关数据
海关编码 2907299090
海关数据

中国海关编码:

2907299090

概述:

2907299090 其他多元酚,酚醇。监管条件:AB(入境货物通关单,出境货物通关单)。增值税率:17.0%。退税率:9.0%。最惠国关税:5.5%。普通关税:30.0%

申报要素:

品名, 成分含量, 用途

监管条件:

A.入境货物通关单
B.出境货物通关单

检验检疫类别:

R.进口食品卫生监督检验
S.出口食品卫生监督检验
M.进口商品检验
N.出口商品检验

Summary:

2907299090 polyphenols; phenol-alcohols。supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward)。VAT:17.0%。tax rebate rate:9.0%。MFN tariff:5.5%。general tariff:30.0%

合成路线

合成路线:1 步

反应条件:
参考文献:
A novel "pro-sensitizer" based sensing of enzymes using Tb(III) luminescence in a hydrogel matrix
Bhowmik, Sandip; Maitra, Uday, Chemical Communications (Cambridge, 2012, 48(38), 4624-4626

合成路线:1 步

反应条件:
参考文献:
Practical Cleavage of Acetals by Using an Odorless Thiol Immobilized on Silica
de Leseleuc, Mylene; Kukor, Andrew; Abbott, Shaun D.; Zacharie, Boulos, European Journal of Organic Chemistry, 2019, 2019(44), 7389-7393

合成路线:1 步

反应条件:
参考文献:
Regioselective hydrolysis of diacetoxynaphthalenes catalyzed by Pseudomonas sp. lipase in an organic solvent
Ciuffreda, Pierangela; Casati, Silvana; Santaniello, Enzo, Tetrahedron, 1999, 56(2), 317-321

合成路线:1 步

参考文献:
An efficient synthesis of dinaphthothiophene derivatives
Sadorn, Karoon; Sinananwanich, Warapon; Areephong, Jetsuda; Nerungsi, Chakkrapan; Wongma, Chalayut; et al, Tetrahedron Letters, 2008, 49(29-30), 4519-4521

合成路线:1 步

反应条件:
参考文献:
Quinone methides and fuchsones. XXVII. Oxidative rearrangement of o-fuchsone to 2,2-diphenyl-1,3-benzodioxole
Pisova, Milena; Soucek, Milan, Collection of Czechoslovak Chemical Communications, 1982, 47(12), 3318-27

合成路线:1 步

参考文献:
Purification of 2,3-dihydroxynaphthalene
, Japan, , ,

合成路线:1 步

参考文献:
Hydroxylation of phenolic compounds using ultrasound in aqueous solution
Takizawa, Yasuomi; Akama, Madoka; Yoshihara, Nobutoshi; Nojima, Osamu; Arai, Kowashi; et al, Ultrasonics Sonochemistry, 1996, 3(3),

合成路线:1 步

参考文献:
Studies of Claisen rearrangement of bispropargyl ethers. Synthesis of naphthodipyrans, naphthodifurans and naphthofuropyrans
Venugopalan, Bindumadhavan; Balasubramanian, Kalpattu Kuppuswamy, Heterocycles, 1985, 23(1), 81-92

合成路线:1 步

反应条件:
参考文献:
Method for synthesizing 2,3-dihydroxynaphthalene
, China, , ,

合成路线:1 步

参考文献:
Method for the preparation of aryl alcohol or heteroaryl alcohol
, Korea, , ,

合成路线:1 步

参考文献:
Molecular design, chemical synthesis, kinetic studies, calculations, and biological studies of novel enediynes equipped with triggering, detection, and deactivating devices. Model dynemicin A epoxide and cis-diol systems
Nicolaou, K. C.; Dai, W. M.; Hong, Y. P.; Baldridge, K. K.; Siegel, J. S.; et al, Journal of the American Chemical Society, 1993, 115(18), 7944-53

合成路线:1 步

参考文献:
Synthesis of some naphtholamines
Behforouz, Mohammad; Carmack, Marvin, Iranian Journal of Science and Technology, 1979, 7(3), 153-5

合成路线:1 步

反应条件:
参考文献:
Preparation of 2,3-dihydroxynaphthalene in presence of ionic liquid catalyst
, China, , ,

合成路线:1 步

反应条件:
参考文献:
Synthesis of substituted benzo-1,3-dioxolanes, dioxanes and benzo-1,4-dioxolanes
Zlotskiy, S. S.; Mikhaylova, N. N.; Bogomazova, A. A.; Kazakova, A. N., Entsiklopediya Inzhenera-Khimika, 2012, (6), 22-28

合成路线:1 步

反应条件:
参考文献:
An efficient strategy for protecting dihydroxyl groups of catechols
Huang, Wei-Bin; Guo, Ying; Jiang, Jian-An; Pan, Xian-Dao; Liao, Dao-Hua; et al, Synlett, 2013, 24(6), 741-746

合成路线:1 步

反应条件:
参考文献:
Microbial screening of thorium(IV) and dioxouranium(VI) chelates with oxine and phenols
Kapadia, M. A.; Patel, M. M.; Patel, G. P.; Joshi, J. D., Journal of the Indian Chemical Society, 2007, 84(7), 637-639

合成路线:1 步

反应条件:
参考文献:
Preparation of indoles and other (hetero)arenes for treating protein folding disorders
, World Intellectual Property Organization, , ,

合成路线:1 步

参考文献:
Chemistry of anti- and syn-1,2:3,4-naphthalene dioxides and their potential relevance as metabolic intermediates
Tsang, Wing Sum; Griffin, Gary W.; Horning, M. G.; Stillwell, W. G., Journal of Organic Chemistry, 1982, 47(27), 5339-53

合成路线:1 步

参考文献:
Synthesis and use of ortho-(branched alkoxy)-tert-butoxybenzenes
Rast, Slavko; Stephan, Michel; Mohar, Barbara, Tetrahedron Letters, 2012, 53(50), 6815-6818

合成路线:1 步

参考文献:
Synthesis of dinaphtho-18-crown-6 and naphtho-15-crown-5
Qin, Shengying, Huaxue Shiji, 1987, 9(4), 203-4
相关文献
专业数据库参考
PubChemId 7091
参考资料
Reaxys RN 742375
Beilstein 742375
产品用途
用于制偶氮染料等
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