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61775-34-6

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61775-34-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61775-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61775-34:
(7*6)+(6*1)+(5*7)+(4*7)+(3*5)+(2*3)+(1*4)=136
136 % 10 = 6
So 61775-34-6 is a valid CAS Registry Number.

61775-34-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name PhCH2SSCO2Me

1.2 Other means of identification

Product number -
Other names Benzylsulfenyl methyl thiocarbonate

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:61775-34-6 SDS

61775-34-6Relevant articles and documents

Esterase-Activated Perthiocarbonate Persulfide Donors Provide Insights into Persulfide Persistence and Stability

Cerda, Matthew M.,Fosnacht, Kaylin G.,Mullen, Emma J.,Pigg, Hannah C.,Pluth, Michael D.

, (2022/01/28)

Persulfides (RSSH) are important reactive sulfur species (RSS) that are intertwined with the biological functions of hydrogen sulfide (H2S). The direct study of persulfides is difficult, however, due to their both nucleophilic and electrophilic

Triphenylphosphine Decomposition of Sulfenyl Thiocarbonates

Harpp, David N.,Granata, Alessandro

, p. 271 - 273 (2007/10/02)

Several sulfenyl thiocarbonates (RSSCO2CH3) have been decomposed with triphenylphosphine.In the case of R = alkyl, desulfurization takes place to give the S-alkyl thiocarbonate while in the case of R = aryl, a phosphonium salt is likely formed which on chromatographic workup on silica gel is converted to a thiol and triphenylphosphine oxide and sulfide.A mechanistic interpretation is offered.

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