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197014-35-0

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197014-35-0 Usage

Antioxidant

BHT-DMS is commonly used as an antioxidant in various consumer products, particularly in polymeric materials and pharmaceuticals.

Stabilizer

It helps maintain the potency and shelf life of pharmaceutical products by preventing oxidation and degradation.

Free radical scavenger

BHT-DMS prevents oxidation and degradation of materials by scavenging free radicals.

Inhibits chain reactions

It inhibits chain reactions that lead to product degradation, thus preserving the quality of materials.

Protecting group

BHT-DMS has potential applications in organic synthesis as a protecting group for phenolic hydroxyl groups.

Check Digit Verification of cas no

The CAS Registry Mumber 197014-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,0,1 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 197014-35:
(8*1)+(7*9)+(6*7)+(5*0)+(4*1)+(3*4)+(2*3)+(1*5)=140
140 % 10 = 0
So 197014-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H34O3Si2/c1-17(2,3)22(7,8)20-14-12-11-13-15(16(14)19)21-23(9,10)18(4,5)6/h11-13,19H,1-10H3

197014-35-0SDS

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 2,6-bis[[tert-butyl(dimethyl)silyl]oxy]phenol

1.2 Other means of identification

Product number -
Other names 2,5,6-TRICHLORO-3-TRIFLUOROMETHYLPYRIDINE

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:197014-35-0 SDS

197014-35-0Downstream Products

197014-35-0Relevant articles and documents

Synthesis of 1-hydroxybicyclo[3.2.1]oct-3-en-2-ones by Acyloin rearrangement of 1-methoxy- or 1-tert-butyldimethylsilyloxybicyclo [2.2.2] oct-5-en-2-ones

Katayama, Sadamu,Hiramatsu, Hajime,Aoe, Keiichi,Yamauchi, Masashige

, p. 1419 - 1427 (1997)

1-Hydroxy-or 1,8-dihydroxy-bicyclo[3,2,1]oct-3-en-2-ones were obtained from 1-methoxy- or 1-tert-butyldimethylsilyloxy-bicyclo[2,2,2]oct-5-en-2- ones via successive processes involving demethylation or desilylation and acyloin rearrangement by reaction wi

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