5-Bromoindole-2-carboxylic acid

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1 Gram	Negotiable

1 Gram

Negotiable

Min.Order :1 Gram
Purity: 98% purity
Payment Terms : T/T,,MoneyGram,Other

Keywords

5-Bromoindole-2-carboxylic acid 7254-19-5 98% purity

Quick Details

Appearance:powder
Application:intermediate
PackAge:according to the need pf packing
ProductionCapacity:100|Kilogram|Day
Storage:sealed in dry, room temperature
Transportation:air，sea and courier

Superiority:

Product Name:   5-Bromoindole-2-carboxylic acid
Synonyms:   5-BROMO-1H-INDOLE-2-CARBOXYLIC ACID;5-BROMO-2-INDOLECARBOXYLIC ACID;5-BROMOINDOLE-2-CARBOXYLIC ACID;AKOS JY2082545;1H-INDOLE-2-CARBOXYLIC ACID, 5-BROMO-;5-bromoindole-2-carboxylicacid5-Bromoindole-2-carboxylicacid;5-Bromoindole-2-carboxylic acid ,98%;5-BroMo-1H-indol-2-carboxylic acid
CAS:   7254-19-5
MF:   C9H6BrNO2
MW:   240.05
EINECS:
Mol File:   7254-19-5.mol

Details:

Melting point    287-288
Boiling point    470.9±25.0 °C(Predicted)
density    1.838±0.06 g/cm3(Predicted)
storage temp.    -20°C
pka   4.25±0.30(Predicted)
form    Solid
CAS DataBase Reference   7254-19-5(CAS DataBase Reference)
Safety Information
Hazard Codes    Xi
Risk Statements    36/37/38
Safety Statements    26-37/39-36/37/39
WGK Germany    3
Hazard Note    Irritant
HazardClass    IRRITANT
HS Code    29339980
MSDS Information
Provider   Language
SigmaAldrich   English
5-Bromoindole-2-carboxylic acid Usage And Synthesis
Uses   5-Bromoindole-2-carboxylic acid,Reactant involved in studies of biologically active molecules including:Discovery of indole inhibitors of MMP-13 for treatment of arthritic diseases1;Synthesis of indolyl ethanones as indoleamine 2,3-dioxygenase inhibitors2 ;cis-Diaminocyclohexane derivatives prepared for use as factor Xa inhibitors3 ;Synthesis of tubulin polymerization inhibitors and cancer cell growth inhibitors4 ;Preparation of dual PPARγ/δ agonists5;Synthesis of chemical probes to examine the role of hFPRL1 receptor .
5-Bromoindole-2-carboxylic acid Preparation Products And Raw materials
Raw materials   Ethanol-->Polyphosphoric acid-->Ethyl pyruvate-->Lithium hydroxide-->4-BROMOPHENYLHYDRAZINE HYDROCHLORIDE
Preparation Products   2-(Ethoxycarbonyl)-5-bromo-indole-->5-Bromoindole-2-carboxylic acid methyl ester