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103711-22-4

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103711-22-4 Usage

Chemical Family

Carboxylic acids
The compound belongs to the family of carboxylic acids, which are organic compounds with a carboxyl functional group (-COOH).

Derivative of Acetic Acid

It is a derivative of acetic acid, meaning it is structurally similar to acetic acid but has modifications to its chemical structure, such as the addition of a benzyl group and an isopropylthio group.

Benzyl Group

A benzyl group (C6H5CH2-) is attached to the carbon atom in the compound, which is an aromatic group known for its stability and aromaticity.

Isopropylthio Group

An isopropylthio group (CH3CH(CH3)S-) is also attached to the carbon atom, which is a sulfur-containing alkyl group that can impart unique properties to the compound.

Potential Applications

The compound has potential applications in organic synthesis and chemical research, making it a valuable substance for further exploration and development.

Building Block in Pharmaceutical Production

It may be used as a building block in the production of various pharmaceuticals, contributing to the development of new drugs and medications.

Use in Agrochemicals

The compound can also be used in the production of agrochemicals, such as pesticides and fertilizers, to improve agricultural productivity and crop protection.

Synthesis of Complex Molecules

Its unique structure and properties make it a valuable intermediate in the synthesis of more complex molecules, which can have diverse industrial and biological applications.

Industrial and Biological Applications

The compound's versatility and potential for further development make it suitable for a wide range of applications in both industrial and biological settings.

Check Digit Verification of cas no

The CAS Registry Mumber 103711-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,7,1 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103711-22:
(8*1)+(7*0)+(6*3)+(5*7)+(4*1)+(3*1)+(2*2)+(1*2)=74
74 % 10 = 4
So 103711-22-4 is a valid CAS Registry Number.

103711-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(phenylmethoxycarbonylamino)-2-propan-2-ylsulfanylacetic acid

1.2 Other means of identification

Product number -
Other names N-Benzyloxycarbonyl-2-isopropylthioglycine

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:103711-22-4 SDS

103711-22-4Relevant articles and documents

AZEPIN-2-ONE DERIVATIVES AS RSV INHIBITORS

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Page/Page column 53, (2019/05/30)

The present invention discloses compounds of Formula (I), or pharmaceutically acceptable salts, esters, or prodrugs thereof: which inhibit Respiratory Syncytial Virus (RSV). The present invention further relates to pharmaceutical compositions comprising the aforementioned compounds for administration to a subject suffering from RSV infection. The invention also relates to methods of treating an RSV infection in a subject by administering a pharmaceutical composition comprising the compounds of the present invention.

The synthesis and conformational aspects of a novel dioxopiperazine - A possible β-turn constraint

Davies, John S.,Stelmach-Diddams, Malgosia,Fromentin, Regis,Howells, Alun,Cotton, Ron

, p. 239 - 243 (2007/10/03)

The synthesis and conformational aspects of a dioxopiperazine was discussed. The cis configuration of the dioxopiperazine was rationalized using nuclear magnetic resonance (NMR) spectroscopy. Computational energy calculations were performed to explain the reluctance to cyclise of N-terminal partially protected dipeptides containing α, α-amino groups.

Phosphotyrosine peptidomimetics for inhibiting SH2 domain interactions

-

, (2008/06/13)

The present invention makes available novel compounds represented by the general formula STR1 wherein Y represents a phosphate analog. Which compounds are useful for inhibiting an interaction between a protein containing an SH2 domain and a phophotyrosine

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