1H-BENZO(G)INDOLE

Product Name: 1H-BENZO(G)INDOLE
CAS No.: 233-34-1
Chemical Name: 1H-BENZO(G)INDOLE
Synonyms: NSC 153687;6,7-Benzindole;1H-Benz[g]indole;1H-BENZO(G)INDOLE;1H-Benzo[g]indole 97%;1H-Benz[g]indole 6,7-Benzindole NSC 153687
CBNumber: CB3972764
Molecular Formula: C12H9N
Formula Weight: 167.21
MOL File: 233-34-1.mol

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1H-BENZO(G)INDOLE Property

Melting point:: 180-184 °C
Boiling point:: 371.1±11.0 °C(Predicted)
Density: 1.229±0.06 g/cm3(Predicted)
pka: 17.00±0.30(Predicted)
EPA Substance Registry System: 1H-Benz[g]indole (233-34-1)

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Safety

Hazard Codes: Xn
Risk Statements: 22-41
Safety Statements: 26
RIDADR: UN 2811 6.1/PG 3
WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H301Toxic if swalloed

H318Causes serious eye damage

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 684910
Product name: 1H-Benzo[g]indole
Purity: 97%
Packaging: 1g
Price: $90
Updated: 2024/03/01

AK Scientific

Product number: 0713AQ
Product name: 1H-Benzo[g]indole
Packaging: 1g
Price: $167
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0114781
Product name: 1H-BENZO[G]INDOLE
Purity: 95.00%
Packaging: 1G
Price: $692.36
Updated: 2021/12/16

aablocks

Product number: AA00C3SL
Product name: 1H-Benzo[g]indole
Purity: 95%
Packaging: 1g
Price: $165
Updated: 2021/12/16

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1H-BENZO(G)INDOLE Chemical Properties,Usage,Production

Uses

Reactant for preparation of tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators

1H-BENZO(G)INDOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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1H-BENZO(G)INDOLE Suppliers

China 17 Switzerland 1 United States 3 Global 21

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233-34-1, 1H-BENZO(G)INDOLERelated Search:

2-Hydroxy-N-(4-methoxyphenyl)-11H-benzo[a]carbazole-3-carboxamide 1,2：7,8-Dibenzocarbazole 2-hydroxy-11H-benzo[a]carbazole-3-carboxylic acid 1H-Benzo[g]indole-3-carboxaldehyde 11H-Benzo(a)carbazole, 2-chloro- [1,2]benzisothiazolo[2,3,4-lma]benzo[h]quinoxalino[2,3-c]carbazole-11,16-dione 9,9-dioxide 11H-BENZO[A]CARBAZOLE 1H-BENZO(G)INDOLE 1H-BENZO[G]INDOLE-2-CARBOXYLIC ACID ETHYL 5-(2-ETHOXY-2-OXOETHOXY)-1-ISOBUTYL-2-METHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE NAPTHOL AS-SG AKOS E-2364 ETHYL 5-[(4-FLUOROBENZOYL)OXY]-1,2-DIMETHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE ETHYL 1-(2-[3-(ETHOXYCARBONYL)-5-METHOXY-2-METHYL-1H-BENZO[G]INDOL-1-YL]ETHYL)-5-METHOXY-2-METHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE ETHYL 1-BENZYL-5-(2-ETHOXY-2-OXOETHOXY)-2-METHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE ETHYL 1-(2-[3-(ETHOXYCARBONYL)-5-HYDROXY-2-METHYL-1H-BENZO[G]INDOL-1-YL]ETHYL)-5-HYDROXY-2-METHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE ETHYL 1-(2,4-DIMETHYLPHENYL)-5-HYDROXY-2-METHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE AKOS E-2365

1H-BENZO(G)INDOLE

6,7-Benzindole

NSC 153687

1H-Benzo[g]indole 97%

1H-Benz[g]indole 6,7-Benzindole NSC 153687

1H-Benz[g]indole

233-34-1