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101250-73-1

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101250-73-1 Usage

Description

(S)-2-MercaptoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is a chemical compound characterized by its unique structure, which includes a pyrrolidine ring, a carboxylic acid group, and a benzyl ester. As a chiral molecule, it possesses a non-superimposable mirror image, making it valuable in the production of enantiopure compounds. Its functional groups and mercapto group contribute to its versatility in various chemical reactions and the synthesis of sulfur-containing compounds, establishing it as a significant intermediate in organic chemistry.

Uses

Used in Pharmaceutical Industry:
(S)-2-MercaptoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is used as a building block for the synthesis of pharmaceuticals due to its versatile reactivity and chiral nature, which allows for the production of enantiopure compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-2-MercaptoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is used as a key component in the development of new agrochemicals, leveraging its functional groups and reactivity to create compounds with specific pesticidal or herbicidal properties.
Used in Fine Chemicals Production:
(S)-2-MercaptoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is utilized as an intermediate in the production of various fine chemicals, taking advantage of its unique structure and functional groups to synthesize complex molecules with specific applications.
Used in Organic Synthesis:
As a versatile reagent in organic synthesis, (S)-2-MercaptoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is used for its ability to participate in a wide range of chemical reactions, including thiol-specific reactions, which are essential for the synthesis of sulfur-containing compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 101250-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,5 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 101250-73:
(8*1)+(7*0)+(6*1)+(5*2)+(4*5)+(3*0)+(2*7)+(1*3)=61
61 % 10 = 1
So 101250-73-1 is a valid CAS Registry Number.

101250-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-phenylmethyl 2-(mercaptomethyl)-1-pyrrolidinecarboxylate

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:101250-73-1 SDS

101250-73-1Relevant articles and documents

Simple preparation of N-protected chiral-amino alkyl thiols from corresponding iodides employing sodium trithiocarbonate

Madhu, Chilakapati,Hemantha, H. P.,Vishwanatha, T. M.,Sureshbabu, V. V.

, p. 228 - 235,8 (2020/09/02)

A simple protocol for the preparation of N-protected amino alkyl thiols is reported that employs a reaction of sodium trithiocarbonate (Na 2CS3) with N-protected amino alkyl iodides. Na 2CS3 is easy to prepare and the protocol circumvents the use of strong bases and multiple steps. All the thiol compounds made were obtained as enantiopure samples and were characterized employing NMR and mass spectrometry.

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