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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Aromatic acids >benzofuran-6-carboxylic acid

benzofuran-6-carboxylic acid

benzofuran-6-carboxylic acid Structure
  • ₹0
  • Product name: benzofuran-6-carboxylic acid
  • CAS: 77095-51-3
  • MF: C9H6O3
  • MW: 162.14
  • EINECS:
  • MDL Number:MFCD01006751
  • Synonyms:benzofuran-6-carboxylic acid;Lifitegrast Intermediate 1;Benzofuran-6-Caboxylic Acid;Lifitegrast Impurity 29;6-Benzofurancarboxylic acid;1-benzofuran-6-carboxylic acid;6-Benzofurancarboxylic acid / Lifitegrast intermediate;1-Piperazinecarboxylicacid,4-(2-bromoethyl)-,1,2-dimethylethylester
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :>182°C (dec.)
Boiling point :325.6±15.0 °C(Predicted)
Density :1.363
storage temp. :Sealed in dry,Room Temperature
solubility :DMSO (Slightly), Methanol (Slightly)
form :Solid
pka :4.02±0.30(Predicted)
color :Dark Yellow to Very Dark Yellow
CAS DataBase Reference :77095-51-3

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Benzofuran-6-carboxylic Acid is a reagent in the development of potent LFA-1/ICAM antagonist SAR 118 as an opthalmic solution for treating dry eyes. Preparation of piperidinylpyrimidine derivatives as inhibitors of HIV-1 LTR activation.

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