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28539-02-8

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28539-02-8 Usage

Description

1H-Benzotriazole-1-methanol is an organic compound with the molecular formula C7H7N3O and is characterized by its heterocyclic structure containing a benzene ring fused to a triazole ring. It is a versatile molecule with various applications across different industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
1H-Benzotriazole-1-methanol is used as a catalyst for the hydrolysis of phenyl esters of α-furoic acid, which is an important step in the synthesis of various pharmaceutical compounds.
Used in Chemical Industry:
1. 1H-Benzotriazole-1-methanol is used as a corrosion inhibitor of iron in aerated acidic media, protecting metal surfaces from degradation and extending their lifespan.
2. It serves as a reactive oxygen scavenger, neutralizing reactive oxygen species that can cause damage to materials and structures.
Used in Synthesis:
1. 1H-Benzotriazole-1-methanol is used as a reactant for the synthesis of hydroxy-skipped bis-homo-inositol derivatives, which have potential applications as glycosidase inhibitors.
2. It is utilized in the enantioselective synthesis of aplysin, a natural product with potential pharmaceutical applications, through a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangement.
3. 1H-Benzotriazole-1-methanol is also used in the synthesis of substituted dihydroquinoline carboxylic acids, which have been identified as potential antitumor and HIV-1 integrase inhibitors.
4. Additionally, 1H-Benzotriazole-1-methanol is employed in the Gosteli-Claisen rearrangement, a chemical reaction that involves the rearrangement of allyl vinyl ethers to γ,δ-unsaturated alcohols, which are valuable synthetic intermediates in the preparation of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 28539-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,3 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28539-02:
(7*2)+(6*8)+(5*5)+(4*3)+(3*9)+(2*0)+(1*2)=128
128 % 10 = 8
So 28539-02-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O/c11-5-10-7-4-2-1-3-6(7)8-9-10/h1-4,11H,5H2

28539-02-8 Well-known Company Product Price

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  • Aldrich

  • (410233)  1H-Benzotriazole-1-methanol  98%

  • 28539-02-8

  • 410233-10G

  • 526.50CNY

  • Detail
  • Aldrich

  • (410233)  1H-Benzotriazole-1-methanol  98%

  • 28539-02-8

  • 410233-50G

  • 1,776.06CNY

  • Detail

28539-02-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name benzotriazol-1-ylmethanol

1.2 Other means of identification

Product number -
Other names 1-Benzotriazolemethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28539-02-8 SDS

28539-02-8Relevant articles and documents

N-Hydroxymethylation of 3-Aryl-2-cyanoprop-2-enethioamides

Chigorina, E. A.,Dotsenko, V. V.,Krivokolysko, S. G.

, p. 1411 - 1417 (2020/09/21)

Abstract: Hydroxymethylation of (E)-3-aryl-2-cyanoprop-2-enethioamides with an aqueous alcoholic solution of formaldehyde has afforded (E)-3-aryl-N-(hydroxymethyl)-2-cyanoprop-2-enethioamides. The predictive analysis of the biological activity of the obtained compounds in silico has been carried out.

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