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1-benzyl-5-broMo-1H-benzo[d][1,2,3]triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1242069-38-0

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1242069-38-0 Usage

Type of compound

Benzotriazole derivative

Common uses

Corrosion inhibitor
UV stabilizer
Antifungal agent

Additional properties

Inhibits growth of algae and bacteria in water

Physical appearance

White to off-white solid

Solubility

Sparingly soluble in water
Soluble in organic solvents (e.g., ethanol, methanol)

Industrial applications

Various

Ongoing research

Potential new uses in pharmaceuticals and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 1242069-38-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,2,0,6 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1242069-38:
(9*1)+(8*2)+(7*4)+(6*2)+(5*0)+(4*6)+(3*9)+(2*3)+(1*8)=130
130 % 10 = 0
So 1242069-38-0 is a valid CAS Registry Number.

1242069-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-5-bromo-1H-benzo[d][1,2,3]triazole

1.2 Other means of identification

Product number -
Other names 1-benzyl-5-bromo-1H-benzotriazole

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:1242069-38-0 SDS

1242069-38-0Downstream Products

1242069-38-0Relevant articles and documents

2-[(Neopentyl glycolato)boryl]phenyl Triflates and Halides for Fluoride Ion-Mediated Generation of Functionalized Benzynes

Ikawa, Takashi,Yamamoto, Rika,Takagi, Akira,Ito, Toyohiro,Shimizu, Kazunori,Goto, Masahiko,Hamashima, Yoshitaka,Akai, Shuji

, p. 2287 - 2300 (2015/07/27)

2-[(Neopentyl glycolato)boryl]phenyl trifluoromethanesulfonates (triflates) and halides have been developed as new benzyne precursors, which generate benzynes at 120°C in the presence of a fluoride ion. There are two major features of these types of precu

An alkynylboronate cycloaddition strategy to functionalised benzyne derivatives

Kirkham, James D.,Delaney, Patrick M.,Ellames, George J.,Row, Eleanor C.,Harrity, Joseph P. A.

supporting information; experimental part, p. 5154 - 5156 (2010/10/19)

A new approach to benzyne precursors has been developed that involves the [4+2] cycloaddition of trimethylsilyl alkynylboronates with 2-pyrones, followed by oxidation and trifluoromethylsulfonylation of the boronate moiety. The Royal Society of Chemistry

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