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35065-97-5

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35065-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35065-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35065-97:
(7*3)+(6*5)+(5*0)+(4*6)+(3*5)+(2*9)+(1*7)=115
115 % 10 = 5
So 35065-97-5 is a valid CAS Registry Number.

35065-97-5SDS

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 S-2-phenylethyl thioacetate

1.2 Other means of identification

Product number -
Other names S-phenethyl ethanethioate

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:35065-97-5 SDS

35065-97-5Relevant articles and documents

Transition metal photoredox catalysis of radical thiol-ene reactions

Tyson, Elizabeth L.,Ament, Michael S.,Yoon, Tehshik P.

, p. 2046 - 2050 (2013/03/29)

We describe the anti-Markovnikov hydrothiolation of olefins using visible-light-absorbing transition metal photocatalysts. The key thiyl radical intermediates are generated upon quenching of photoexcited Ru*(bpz) 32 with a variety of thiols. The adducts of a wide variety of olefins and thiols are formed in excellent yield (73-99%).

An efficient one-pot synthesis of unsymmetrical ethers: A directly reductive deoxygenation of esters using an InBr3/Et3SiH catalytic system

Sakai, Norio,Moriya, Toshimitsu,Konakahara, Takeo

, p. 5920 - 5922 (2008/02/09)

(Chemical Equation Presented) This study describes a novel one-pot procedure for a directly reductive conversion of the carbonyl function of esters to the corresponding ethers by Et3SiH in the presence of a catalytic amount of InBr3.

Inhibition of human cytomegalovirus protease N(o) with monocyclic β- lactams

Deziel,Malenfant

, p. 1437 - 1442 (2007/10/03)

Monocyclic β-lactams have been identified as potent and selective inhibitors of the human cytomegalovirus protease (HCMV) N(o). Two series of these inhibitors are described, a peptidyl series of compounds and non- peptidic molecules featuring lower molecular weights. The SAR work that lead to the discovery of these inhibitors, together with their synthesis is also disclosed.

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