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98051-92-4

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98051-92-4 Usage

General Description

The chemical "(disulfanediyldibenzene-2,1-diyl)bis(1H-benzotriazol-1-ylmethanone)" is a compound with the molecular formula C30H20N6S2O2. It is commonly used as a UV stabilizer in plastics, rubber, and other materials to protect them from degradation caused by UV radiation. (disulfanediyldibenzene-2,1-diyl)bis(1H-benzotriazol-1-ylmethanone) functions by absorbing UV radiation and dissipating it as heat, thereby preventing damage to the material. It is also used in personal care products such as sunscreens and anti-aging creams to provide protection from the sun's harmful UV rays. Additionally, this compound is used in the pharmaceutical industry as a photo-stabilizer for drugs and as an anti-oxidant in polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 98051-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98051-92:
(7*9)+(6*8)+(5*0)+(4*5)+(3*1)+(2*9)+(1*2)=154
154 % 10 = 4
So 98051-92-4 is a valid CAS Registry Number.

98051-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[[2-(benzotriazole-1-carbonyl)phenyl]disulfanyl]phenyl]-(benzotriazol-1-yl)methanone

1.2 Other means of identification

Product number -
Other names Benzotriazolyl 2-((2-(benzotriazolylcarbonyl)phenyl)disulfanyl)phenyl ketone

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:98051-92-4 SDS

98051-92-4Relevant articles and documents

Synthesis of benzoxazines, quinazolines and 4H-benzo[e][1,3]thiazine by ANRORC rearrangements of 1,2,4-oxadiazoles

Draghici, Bogdan,El-Gendy, Bahaa El-Dien M.,Katritzky, Alan R.

supporting information; experimental part, p. 547 - 550 (2012/04/04)

1,2,4-Oxadiazoles undergo ANRORC (addition of nucleophile, ring-opening and ring-closure) rearrangements upon reaction with excess of n-butyllithium to give benzoxazines, benzothiazines, and quinazolines in good yields under mild conditions. Georg Thieme Verlag Stuttgart · New York.

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