5-Bromoindole-2-carboxylic acid

5-Bromoindole-2-carboxylic acid Structure
CAS No.
7254-19-5
Chemical Name:
5-Bromoindole-2-carboxylic acid
Synonyms
5-BROMO-1H-INDOLE-2-CARBOXYLIC ACID;NSC 73384;AKOS JY2082545;5-Bromo-2-carboxy-1H-indole;5-BROMOINDOLE-2-CARBOXYLIC ACID;5-BROMO-2-INDOLECARBOXYLIC ACID;5-Bromoindole-2-carboxylicAcid>5-Bromoindazole-2-carboxylic acid;5-BroMo-1H-indol-2-carboxylic acid;5-Bromoindole-2-carboxylic acid ,98%
CBNumber:
CB0242185
Molecular Formula:
C9H6BrNO2
Molecular Weight:
240.05
MOL File:
7254-19-5.mol
MSDS File:
SDS
Modify Date:
2024/8/7 19:09:42

5-Bromoindole-2-carboxylic acid Properties

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
color White to Light yellow to Light orange
InChI InChI=1S/C9H6BrNO2/c10-6-1-2-7-5(3-6)4-8(11-7)9(12)13/h1-4,11H,(H,12,13)
InChIKey YAULOOYNCJDPPU-UHFFFAOYSA-N
SMILES N1C2=C(C=C(Br)C=C2)C=C1C(O)=O
CAS DataBase Reference 7254-19-5(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H335-H315-H319
Precautionary statements  P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313-P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-37/39-36/37/39
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339980
NFPA 704
1
2 0

5-Bromoindole-2-carboxylic acid price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) B2761 5-Bromoindole-2-carboxylic acid 98% 7254-19-5 1G ₹10500.25 2022-06-14 Buy
TCI Chemicals (India) B3836 5-Bromoindole-2-carboxylic Acid min. 97.0 % 7254-19-5 1G ₹9500 2022-05-26 Buy
Product number Packaging Price Buy
B2761 1G ₹10500.25 Buy
B3836 1G ₹9500 Buy

5-Bromoindole-2-carboxylic acid Chemical Properties,Uses,Production

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

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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 NSC 73384 5-Bromoindazole-2-carboxylic acid 5-Bromo-2-carboxy-1H-indole 5-Bromoindole-2-carboxylicAcid> 5-BROMO-1H-INDOLE-2-CARBOXYLIC ACID 7254-19-5 Br1C9H6N1O2 C9H6BrNO2 Building Blocks Heterocyclic Building Blocks Halogenated Heterocycles Indoles Heterocycles series Indole/indoline/oxindole Indole and Indoline Indoles and derivatives pharmacetical Organic acids Indoles Indole Halogenated Heterocycles Heterocyclic Building Blocks IndolesBuilding Blocks Pharmaceutical Intermediates Building Blocks C7 to C10 C7 to C9 Chemical Synthesis Halogenated Heterocycles Heterocyclic Building Blocks 1