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72773-04-7

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72773-04-7 Usage

General Description

1H-Benzotriazole-1-carboxaldehyde is a chemical compound with the molecular formula C8H6N2O. It is a pale yellow solid that is used in industrial applications as an intermediate in the synthesis of various organic compounds. 1H-Benzotriazole-1-carboxaldehyde is known for its ability to inhibit the corrosion of metals and is often used as a corrosion inhibitor in products such as automotive fluids and industrial lubricants. Additionally, it has been found to have potential as a photoinitiator in polymer chemistry and as a UV stabilizer in plastics and coatings. This versatile compound is also used in the production of pharmaceuticals, dyes, and optical brighteners. However, it is important to handle this chemical with caution as it can be harmful if ingested, inhaled, or comes into contact with skin.

Check Digit Verification of cas no

The CAS Registry Mumber 72773-04-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,7 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72773-04:
(7*7)+(6*2)+(5*7)+(4*7)+(3*3)+(2*0)+(1*4)=137
137 % 10 = 7
So 72773-04-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5N3O/c11-5-10-7-4-2-1-3-6(7)8-9-10/h1-5H

72773-04-7 Well-known Company Product Price

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  • TCI America

  • (B3920)  1H-Benzotriazole-1-carboxaldehyde  >95.0%(GC)

  • 72773-04-7

  • 1g

  • 780.00CNY

  • Detail
  • TCI America

  • (B3920)  1H-Benzotriazole-1-carboxaldehyde  >95.0%(GC)

  • 72773-04-7

  • 5g

  • 2,450.00CNY

  • Detail

72773-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzotriazole-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1H-benzotriazole-1-carboxaldehyde

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:72773-04-7 SDS

72773-04-7Downstream Products

72773-04-7Relevant articles and documents

Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides

Qu, Erdong,Li, Shangzhang,Bai, Jin,Zheng, Yan,Li, Wanfang

supporting information, p. 58 - 63 (2021/12/27)

Herein we report a Ni-catalyzed reductive transamidation of conveniently available N-acyl benzotriazoles with alkyl, alkenyl, and aryl nitro compounds, which afforded various amides with good yields and a broad substrate scope. The same catalytic reaction conditions were also applicable for N-sulfonyl benzotriazoles, which could undergo smooth reductive coupling with nitroarenes and nitroalkanes to afford the corresponding sulfonamides.

Synthesis of new functionalized mono- and diphosphonic acids with five-membered aza-heterocycles moieties

Prishchenko, Andrey A.,Alekseyev, Roman S.,Livantsov, Mikhail V.,Novikova, Olga P.,Livantsova, Ludmila I.,Terenin, Vladimir I.,Petrosyan, Valery S.

, (2017/01/17)

The new functionalized hydroxymethylphosphonic and methylenediphosphonic acids are synthesized via unique reaction of tris(trimethylsilyl)phosphite and N-formyl derivatives of five-membered aza-heterocycles at the presence of effective catalyst—trimethylsilyl triflate.

New functionalized derivatives of mono- and diphosphonic acids substituted with five-membered nitrogen heterocycles

Prishchenko,Livantsov,Novikova,Livantsova,Alekseyev,Terenin,Petrosyan

, p. 342 - 345 (2017/07/12)

New types of (hydroxymethyl)phosphonic and (methylene)diphosphonic acids bearing heterocyclic fragments were synthesized by addition of tris(trimethylsilyl) phosphite to N-formyl derivatives of five-membered nitrogen heterocycles.

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