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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-Benzo[g]indole;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)
form 
solid
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 24 Switzerland 1 United States 4 Global 29
SIGMA-RBI
Tel
--
Fax
--
Country
Switzerland
ProdList
6896
Advantage
91

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
  • 1<i>H</i>-Benzo[<i>g</i>]indole
  • 233-34-1