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ChemicalBook > Product Catalogue >Chemical Reagents >Organic reagents >Boric acid >1H-INDAZOLE-5-BORONIC ACID

1H-INDAZOLE-5-BORONIC ACID

1H-INDAZOLE-5-BORONIC ACID Structure
  • ₹7869.78 - ₹27138.28
  • Product name: 1H-INDAZOLE-5-BORONIC ACID
  • CAS: 338454-14-1
  • MF: C7H7BN2O2
  • MW: 161.95
  • EINECS:
  • MDL Number:MFCD06739151
  • Synonyms:1H-INDAZOLE-5-BORONIC ACID;1H-INDAZOL-5-YL-5-BORONIC ACID;5-INDAZOLYBORONIC ACID;INDAZOLE-5-BORONIC ACID;1H-Indazol-5-ylboronicacid;Boronic acid, B-1H-indazol-5-yl-;Indazol-5-ylboronic acid;INDAZOL-5-YLBORONIC ACID;
2 prices
Selected condition:

Brand

  • Sigma-Aldrich(India)

Package

  • 250MG
  • 1G
  • ManufacturerSigma-Aldrich(India)
  • Product number724017
  • Product description1H-Indazole-5-boronic acid ≥95%
  • Packaging250MG
  • Price₹7869.78
  • Updated2022-06-14
  • Buy
  • ManufacturerSigma-Aldrich(India)
  • Product number724017
  • Product description1H-Indazole-5-boronic acid ≥95%
  • Packaging1G
  • Price₹27138.28
  • Updated2022-06-14
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
Sigma-Aldrich(India) 724017 1H-Indazole-5-boronic acid ≥95% 250MG ₹7869.78 2022-06-14 Buy
Sigma-Aldrich(India) 724017 1H-Indazole-5-boronic acid ≥95% 1G ₹27138.28 2022-06-14 Buy

Properties

Melting point :175-180°C
Boiling point :457.0±37.0 °C(Predicted)
Density :1.42±0.1 g/cm3(Predicted)
storage temp. :2-8°C
form :Crystalline Powder
pka :8.20±0.30(Predicted)
color :White
CAS DataBase Reference :338454-14-1

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
Precautionary statements:
P280 Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Description

Reactant for:
  • Preparation of thieno[3,2-d]pyrimidines as Tpl2 kinase inhibitors
  • Synthesis of pyridinyl benzonaphthyridinones as mTOR inhibitors for the treatment of cancer
  • Novel bisphosphonate inhibitors of human farnesyl pyrophosphate synthase
  • Preparation of diazabicycloheptanes as α7 neurinal nicotinic receptor affectors
  • Preparation of pyrazolopyrimidinamine derivatives with tyrosine and phosphinositide kinase inhibitory activity

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