Welcome to LookChem.com Sign In|Join Free

CAS

  • or

118507-50-9

Post Buying Request

118507-50-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

118507-50-9 Usage

General Description

(2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is a chemical compound that belongs to the class of carbamic acid esters. Its molecular formula is C12H16N2O3 and its molecular weight is 236.26 g/mol. (2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is commonly used as a reagent in organic synthesis and pharmaceutical research. It is known to have potential pharmacological properties and is being studied for its potential use in the development of new therapeutic agents. Its structure consists of a pyrrolidin-3-yl carbamate group attached to a benzyl ester, making it a versatile building block for the synthesis of various organic and pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 118507-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118507-50:
(8*1)+(7*1)+(6*8)+(5*5)+(4*0)+(3*7)+(2*5)+(1*0)=119
119 % 10 = 9
So 118507-50-9 is a valid CAS Registry Number.

118507-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[(3S)-2-oxopyrrolidin-3-yl]carbamate

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:118507-50-9 SDS

118507-50-9Relevant articles and documents

Diphenylsilane as a coupling reagent for amide bond formation

Sayes, Morgane,Charette, André B.

supporting information, p. 5060 - 5064 (2017/11/09)

A simple procedure for amide bond formation using diphenylsilane as a coupling reagent is described. This methodology enables the direct coupling of carboxylic acids with primary and secondary amines, releasing only hydrogen and a siloxane as by-products. Only one equivalent of each partner is needed, providing a more sustainable amidation method producing minimal wastes. This methodology was also extended to the synthesis of peptides and lactams by addition of Hünig's base (DIPEA) and 4-dimethylaminopyridine (DMAP).

Synthesis and biological activity of sulphostin analogues, novel dipeptidyl peptidase IV inhibitors

Abe, Masatoshi,Akiyama, Tetsuo,Umezawa, Yoji,Yamamoto, Keiichiro,Nagai, Masashi,Yamazaki, Hiroko,Ichikawa, Yuh-Ichiro,Muraoka, Yasuhiko

, p. 785 - 797 (2007/10/03)

The structure of sulphostin (1), a novel dipeptidyl peptidase IV (DPP-IV) inhibitor, is consisted of three key functional groups, including a characteristic amino(sulfoamino)phosphinyl group, on a piperidine ring. To examine the relationship between its s

A flexible approach to (S)-3-amino-2-pyrrolidinone derivatives

Tang, Tian,Zhu, Chen,Huang, Pei-Qiang

, p. 121 - 128 (2007/10/03)

Starting from (S)-aspartic acid, a flexible chemoselective approach to (S)-3-amino-2-pyrrolidinone derivatives was reported. The (S)-3-amino-2-pyrrolidinone derivatives thus synthesized are useful templates for designing medicinal interesting compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 118507-50-9