Basic information Safety Supplier Related

1-BENZYLINDOLE-3-CARBOXYLIC ACID

Basic information Safety Supplier Related

1-BENZYLINDOLE-3-CARBOXYLIC ACID Basic information

Product Name:
1-BENZYLINDOLE-3-CARBOXYLIC ACID
Synonyms:
  • 1-(phenylmethyl)-3-indolecarboxylic acid
  • 1-(phenylmethyl)indole-3-carboxylic acid
  • INDOLE-3-CARBOXYLIC ACID, 1-BENZYL-
  • 1H-Indole-3-carboxylicacid, 1-(phenylmethyl)-
  • RARECHEM AL BE 0270
  • 1-benzyl-indole-3-carboxylicaci
  • 1-BENZYLINDOLE-3-CARBOXYLIC ACID
  • 1-BENZYL-1H-INDOLE-3-CARBOXYLIC ACID
CAS:
27018-76-4
MF:
C16H13NO2
MW:
251.28
Product Categories:
  • Indole
  • Building Blocks
  • Heterocyclic Building Blocks
  • Indoles
  • Building Blocks
  • Heterocyclic Building Blocks
  • C13 to C27
  • Chemical Synthesis
Mol File:
27018-76-4.mol
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1-BENZYLINDOLE-3-CARBOXYLIC ACID Chemical Properties

Melting point:
195-196 °C(Solv: ethanol (64-17-5))
Boiling point:
496.3±28.0 °C(Predicted)
Density 
1.19±0.1 g/cm3(Predicted)
storage temp. 
-20°C
form 
Solid
pka
3.98±0.10(Predicted)
CAS DataBase Reference
27018-76-4(CAS DataBase Reference)
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Safety Information

WGK Germany 
3
RTECS 
NL5995800
HS Code 
29339980
Toxicity
mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#03773,

MSDS

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1-BENZYLINDOLE-3-CARBOXYLIC ACID Usage And Synthesis

Uses

Reactant for preparation of:• ;Indoleacetic acid analogs as differentiation-inducing and antiproliferative agents for human myeloblastoma cells1• ;Indole-carboxamide derivatives as inhibitors of lipid peroxidation and superoxide anion formation2• ;Indole carboxamides as hyaluronidase inhibitors3• ;Fuconojirimycin derivatives as inhibitors of α-fucosidases4• ;Indole-2 and 3-carboxamides as selective cyclooxygenase-2 inhibitors5• ;Indole amides as antihistaminic agents6

Uses

Reactant for preparation of:

  • Indoleacetic acid analogs as differentiation-inducing and antiproliferative agents for human myeloblastoma cells
  • Indole-carboxamide derivatives as inhibitors of lipid peroxidation and superoxide anion formation
  • Indole carboxamides as hyaluronidase inhibitors
  • Fuconojirimycin derivatives as inhibitors of α-fucosidases
  • Indole-2 and 3-carboxamides as selective cyclooxygenase-2 inhibitors
  • Indole amides as antihistaminic agents

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