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4628-56-2

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4628-56-2 Usage

General Description

3-[(1-phenylethyl)amino]propane-1-thiol, also known as N-phenethyl-3-propanethiol, is a chemical compound that belongs to the class of organic compounds known as thioethers. 3-[(1-phenylethyl)amino]propane-1-thiol has a molecular formula of C11H17NS and a molecular weight of 191.32 g/mol. It is a colorless to light yellow liquid with a strong, unpleasant odor. 3-[(1-phenylethyl)amino]propane-1-thiol is used as a flavoring agent and is commonly found in foods, beverages, and fragrances. It is also known for its potential application as an insect repellent and has been used as a natural flavoring substance in the food industry.

Check Digit Verification of cas no

The CAS Registry Mumber 4628-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,2 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4628-56:
(6*4)+(5*6)+(4*2)+(3*8)+(2*5)+(1*6)=102
102 % 10 = 2
So 4628-56-2 is a valid CAS Registry Number.

4628-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-((1-phenylethyl)amino)propane-1-thiol

1.2 Other means of identification

Product number -
Other names -

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:4628-56-2 SDS

4628-56-2Relevant articles and documents

Peptide ligation assisted by an auxiliary attached to amidyl nitrogen

Li, Juan,Cui, Hong-Kui,Liu, Lei

scheme or table, p. 1793 - 1796 (2010/06/13)

New thiol-containing auxiliaries were developed for peptide ligation. They were placed at the amidyl N-atom in the second amino acid residue of a peptide fragment. With the new auxiliaries, peptide ligation could be conducted at non-Cys and non-Gly sites. Compared to other recently developed auxiliaries, an important feature of the present design was that the new auxiliaries were generally applicable and readily removable.

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