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3287-17-0

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3287-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3287-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3287-17:
(6*3)+(5*2)+(4*8)+(3*7)+(2*1)+(1*7)=90
90 % 10 = 0
So 3287-17-0 is a valid CAS Registry Number.

3287-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-tert-butyl-2-(5-chlorobenzotriazol-2-yl)phenol

1.2 Other means of identification

Product number -
Other names -

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:3287-17-0 SDS

3287-17-0Downstream Products

3287-17-0Relevant articles and documents

Preparation of 2-aryl-2H-benzotriazoles by zinc-mediated reductive cyclization of o-nitrophenylazophenols in aqueous media without the use of organic solvents

Liu, Guo-Bin,Zhao, Hong-Yun,Yang, Hong-Jie,Gao, Xiang,Li, Miao-Kui,Thiemann, Thies

, p. 1637 - 1640 (2008/02/11)

Zinc powder-mediated reductive cyclization of o-nitrophenylazophenols in alkaline solution affords the corresponding 2-aryl-2H-benzotriazoles in high yields under mild reaction conditions. No organic solvents are used in the reaction and only minimal amounts in the work-up.

High molecular weight piperidine derivatives as UV stabilizers

-

, (2008/06/13)

Substituted high molecular weight hindered spiropiperidine compounds and polymer compositions stabilized by these compounds. The spiropiperidine compounds are prepared by reacting hindered 4-piperidinone hydrochloride with an activated benzene, such as resorcinol, in an acid medium.

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