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17612-91-8

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17612-91-8 Usage

Uses

Thioacetic Acid S-(2-Aminoethyl) Ester Hydrochloride could be useful reagent in the preparation of psammaplin A analogs, which are potent histone deacetylase inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 17612-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17612-91:
(7*1)+(6*7)+(5*6)+(4*1)+(3*2)+(2*9)+(1*1)=108
108 % 10 = 8
So 17612-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NOS.ClH/c1-4(6)7-3-2-5;/h2-3,5H2,1H3;1H

17612-91-8SDS

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 Thioacetic acid S-(2-amino-ethyl) ester hydrochloride

1.2 Other means of identification

Product number -
Other names 1-trimethylsiloxy-ethane-2-thiol

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:17612-91-8 SDS

17612-91-8Relevant articles and documents

PRODUCTION PROCESSES OF S- AND O-DIACYLATED GAMMA-GLUTAMYL-CYSTEAMINE PRODRUGS

-

Paragraph 0061; 0066-0067; 0074; 0078-0079, (2020/08/28)

Methods are provided for the synthesis of a compound of formula (X). R2 is selected from -H, -C1-C4-alkyl,-C2-C4-alkenyl and C1-C4-aryl; R3 is selected from -C(O)H and

Synthesis of conjugated diacetylene, metal-chelating monomers for polymerizable monolayer assemblies.

Roy,Mallik

, p. 1877 - 1879 (2007/10/03)

[see structure]. Self-assembled monolayers (SAMs) of thiols on gold have been used for numerous applications. For protein targeting applications, one successful strategy is to use a metal-chelating SAM. It has also been demonstrated that polymerized SAMs

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