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- 2521-07-5
2521-07-5
（name: 9-Methyl-9H-pyrido3,4-bindole）
Product Name：9-Methyl-9H-pyrido3,4-bindole
CAS No：2521-07-5
MF：C12H10N2
MW：182.2212
MDL：MFCD18803860
CID：1066656
PubChem ID：354333385
- 9-methyl-9H-Pyrido[3,4-b]indole
- 9H-Pyrido(3,4-b)indole, 9-methyl-
- 9-Methyl-9H-pyrido(3,4-b)indole
- beta-carboline
- 9-methyl-9H-beta-carboline
- 9H-Pyrido(3,4-b)indole,9-methyl
- 9-methyl-
- 9-methylnorharmane
- A-carboline
- N9-methylbetacarboline
- N-methylnorharmane
- 9-Methyl-β-carboline
- 9-Methyl-beta-carboline
- 9-Methylnorharman
- N-Methylnorharman
- 9H-Pyrido[3,4-b]indole, 9-methyl-
- Norharmane, N-methyl-
- 9-methylpyrido[3,4-b]indole
- MABOIYXDALNSES-UHFFFAOYSA-N
- M2818
- 9-Me-BC/9-methyl-9H-pyrido[3,4-b]indole
- 9-Methylnorharmane
- 9-Methyl-9H-pyrido3,4-bindole
- AKOS025312186
- AKOS025312186
- AKOS025312186
- AKOS025312186
- AKOS025312186
- AKOS025312186
- AKOS025312186
- N-Methylnorharmane
- N-Methylnorharmane
- N-Methylnorharmane
- N-Methylnorharmane
- N-Methylnorharmane
- N-Methylnorharmane
- N-Methylnorharmane
- 9-methyl-beta-carboline
- 9-methyl-beta-carboline
- 9-methyl-beta-carboline
- 9-methyl-beta-carboline
- 9-methyl-beta-carboline
- A904394
- 9-methyl-beta-carboline
- 9-methyl-beta-carboline
- A904394
- A904394
- A904394
- A904394
- 9-METHYL-.BETA.-CARBOLINE
- 9-METHYL-.BETA.-CARBOLINE
- A904394
- A904394
- 9-METHYL-.BETA.-CARBOLINE
- 9-METHYL-.BETA.-CARBOLINE
- 9-METHYL-.BETA.-CARBOLINE
- PD150600
- PD150600
- PD150600
- PD150600
- 9-METHYL-.BETA.-CARBOLINE
- 9-METHYL-.BETA.-CARBOLINE
- GC837J2CCJ
- PD150600
- GC837J2CCJ
- GC837J2CCJ
- PD150600
- GC837J2CCJ
- PD150600
- CS-0102858
- GC837J2CCJ
- CS-0102858
- CS-0102858
- Methyl-9h-pyrido[3,4-b]indole
- CS-0102858
- GC837J2CCJ
- GC837J2CCJ
- Methyl-9h-pyrido[3,4-b]indole
- Methyl-9h-pyrido[3,4-b]indole
- CS-0102858
- AS-61363
- CS-0102858
- CS-0102858
- Methyl-9h-pyrido[3,4-b]indole
- DTXSID50179871
- AS-61363
- AS-61363
- Methyl-9h-pyrido[3,4-b]indole
- Methyl-9h-pyrido[3,4-b]indole
- DTXSID50179871
- 9-methyl-?-carboline
- AS-61363
- DTXSID50179871
- Methyl-9h-pyrido[3,4-b]indole
- AS-61363
- 9-methyl-9h-beta-carboline
- 9-methyl-?-carboline
- AS-61363
- 9-methyl-?-carboline
- AS-61363
- DTXSID50179871
- DTXSID50179871
- MFCD18803860
- 9-methyl-9h-beta-carboline
- 9-methyl-9h-beta-carboline
- DTXSID50179871
- DTXSID50179871
- 9-methyl-?-carboline
- 9-methyl-?-carboline
- MFCD18803860
- MFCD18803860
- 9-methyl-?-carboline
- DB-197640
- 9-methyl-9h-beta-carboline
- 9-methyl-?-carboline
- 9-methyl-9h-beta-carboline
- DB-197640
- DB-197640
- 9-methyl-9h-beta-carboline
- 2521-07-5
- MFCD18803860
- 9-methyl-9h-beta-carboline
- 2521-07-5
- MFCD18803860
- 2521-07-5
- MFCD18803860
- 9-methyl-9h-pyrido[3,4-b]indole
- DB-197640
- 9-methyl-9h-pyrido[3,4-b]indole
- MFCD18803860
- UNII-GC837J2CCJ
- 9-methyl-9h-pyrido[3,4-b]indole
- DB-197640
- DB-197640
- 2521-07-5
- UNII-GC837J2CCJ
- UNII-GC837J2CCJ
- 2521-07-5
- 9-methylnorharman
- DB-197640
- 2521-07-5
- 9-methylnorharman
- 9-methylnorharman
- 9-methyl-9h-pyrido[3,4-b]indole
- 9-methyl-9h-pyrido[3,4-b]indole
- SCHEMBL280032
- 2521-07-5
- SCHEMBL280032
- 9-methyl-9h-pyrido[3,4-b]indole
- SCHEMBL280032
- UNII-GC837J2CCJ
- 9-methyl-9h-pyrido[3,4-b]indole
- UNII-GC837J2CCJ
- UNII-GC837J2CCJ
- 9-methylnorharman
- UNII-GC837J2CCJ
- 9-methylnorharman
- 9-methylnorharman
- SCHEMBL280032
- 9-methylnorharman
- SCHEMBL280032
- SCHEMBL280032
- SCHEMBL280032
- MDL：MFCD18803860
- InChIKey：MABOIYXDALNSES-UHFFFAOYSA-N
- Inchi：1S/C12H10N2/c1-14-11-5-3-2-4-9(11)10-6-7-13-8-12(10)14/h2-8H,1H3
- SMILES：N1(C([H])([H])[H])C2C([H])=NC([H])=C([H])C=2C2=C([H])C([H])=C([H])C([H])=C12
Computed Properties
- 精确分子量: 182.08400
- 氢键供体数量: 0
- 氢键受体数量: 1
- 可旋转化学键数量: 0
- 同位素质量: 182.084
- 重原子数量: 14
- 复杂度: 216
- 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）: 2.3
- 拓扑分子极性表面积: 17.8
Experimental Properties
- LogP: 2.72650
- PSA: 17.82000
- 折射率: 1.658
- 沸点: 367.3°C at 760 mmHg
- 熔点: 105.0 to 109.0 deg-C
- 闪点: 175.9°C
- 溶解度: Very 微溶 (0.2 g/L) (25 ºC),
- 最大波长(λmax): 361(Cyclohexane)(lit.)
- 密度: 1.17±0.1 g/cm3 (20 ºC 760 Torr),
- 1. A transition metal-free approach towards the regioselective synthesis of β-carboline tethered pyrroles and 2,3-dihydro-1H-pyrroles Manpreet Singh,Avijit Kumar Paul,Virender Singh New J. Chem. 2020 44 12370
- 2. In(OTf)3 catalysed an expeditious synthesis of β-carboline–imidazo[1,2-a]pyridine and imidazo[1,2-a]pyrazine conjugates Nisha Devi,Dharmender Singh,Honey,Satbir Mor,Sandeep Chaudhary,Ravindra K. Rawal,Vipin Kumar,Asim K. Chowdhury,Virender Singh RSC Adv. 2016 6 43881
- 3. ZnO-NP assisted synthesis of fluorescent β-carboline C-1 tethered benzimidazole/benzothiazole/benzoxazole derivatives and assessment of their photophysical properties Vipin Kumar,Dharmender Singh,Avijit Kumar Paul,Rahul Shrivastava,Virender Singh New J. Chem. 2019 43 18304
- 4. Natural product inspired design and synthesis of β-carboline and γ-lactone based molecular hybrids Dharmender Singh,Nisha Devi,Vipin Kumar,Chandi C. Malakar,Saloni Mehra,Sunita Rattan,Ravindra K. Rawal,Virender Singh Org. Biomol. Chem. 2016 14 8154
- 5. Metal-free 1,3-dipolar cycloaddition approach towards the regioselective synthesis of β-carboline and isoxazole based molecular hybrids Dharmender Singh,Nisha Devi,Vipin Kumar,Chandi C. Malakar,Saloni Mehra,Ravindra K. Rawal,B. S. Kaith,Virender Singh RSC Adv. 2016 6 88066
- 6. Metal-free propargylation/aza-annulation approach to substituted β-carbolines and evaluation of their photophysical properties Chada Raji Reddy,Mounika Aila,Puppala Sathish,Madoori Mrinalini,Lingamallu Giribabu,Seelam Prasanthkumar,René Grée Org. Biomol. Chem. 2019 17 9291
- 7. Colorimetric and ratiometric fluorescence sensing of water based on 9-methyl pyrido[3,4-b]indole-boron trifluoride complex Toshiaki Enoki,Yousuke Ooyama Dalton Trans. 2019 48 2086
- 8. A cascade A3 coupling strategy towards the regioselective synthesis of β-carboline N-fused pyrrole derivatives with pyridine tethers Vaishali,Chandi C. Malakar,Virender Singh New J. Chem. 2023 47 1186
- 9. An AcOH-mediated metal free approach towards the synthesis of bis-carbolines and imidazopyridoindole derivatives and assessment of their photophysical properties Dharmender Singh,Shubham Sharma,Mukesh Kumar,Inderpreet Kaur,Ravi Shankar,Satyendra Kumar Pandey,Virender Singh Org. Biomol. Chem. 2019 17 835
- 10. Spatiotemporal photo-release of hydrogen sulphide from β-carboline-derived nanoparticles for therapeutic applications Antara Sikder,Rakesh Mengji,Saugat Mondal,Avijit Jana,N. D. Pradeep Singh J. Mater. Chem. B 2023 11 5131
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(CAS:2521-07-5)9-Methyl-9H-beta-carbolinesenfeidaContact & Address Information苏州高新区浒墅关经济技术开发区
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(CAS:2521-07-5)9-Methyl-9H-pyrido3,4-bindoleAmadis Chemical Company LimitedContact & Address Information网周路99号
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