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114408-87-6

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114408-87-6 Usage

Molar mass

160.17 g/mol

Type of compound

Carboxaldehyde derivative of 1-methyl-1H-benzotriazole

Common uses

Corrosion inhibitor in industrial applications (e.g. metalworking fluids and lubricants), potential use in pharmaceuticals and as a UV absorber in sunscreen formulations

Known for

Protecting metal surfaces from corrosion by forming a thin, protective film

Hazard classification

Hazardous chemical (should be handled and disposed of with care to prevent environmental contamination and harm to human health)

Check Digit Verification of cas no

The CAS Registry Mumber 114408-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,0 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114408-87:
(8*1)+(7*1)+(6*4)+(5*4)+(4*0)+(3*8)+(2*8)+(1*7)=106
106 % 10 = 6
So 114408-87-6 is a valid CAS Registry Number.

114408-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-1H-benzotriazole-6-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-methyl-1H-benzo[d][1,2,3]triazole-6-carbaldehyde

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:114408-87-6 SDS

114408-87-6Relevant articles and documents

BAX INHIBITORS AND USES THEREOF

-

Paragraph 00488, (2021/01/23)

A compound having formula (I) or (II) for use inhibiting Bax mediated cell death and/or apoptosis.

Regiocomplementary cycloaddition reactions of boryl- and silylbenzynes with 1,3-dipoles: Selective synthesis of benzo-fused azole derivatives

Ikawa, Takashi,Takagi, Akira,Goto, Masahiko,Aoyama, Yuya,Ishikawa, Yoshinobu,Itoh, Yuji,Fujii, Satoshi,Tokiwa, Hiroaki,Akai, Shuji

, p. 2965 - 2983 (2013/06/26)

Benzo-fused nitrogen-containing heterocycles are abundant in biologically active compounds. One of the most important methods for preparing such heterocycles is the (3 + 2) cycloaddition reaction of benzynes with 1,3-dipolar compounds. However, the reacti

THIAZOLONES FOR USE AS PI3 KINASE INHIBITORS

-

Page/Page column 51; 80, (2008/06/13)

Invented is a method of inhibiting the activity/function of PI3 kinases using substituted thiazolones. Also invented is a method of treating one or more disease states selected from: autoimmune disorders, inflammatory diseases, cardiovascular diseases, ne

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