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121772-98-3

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121772-98-3 Usage

General Description

L-Proline, 2-(2-propenyl)- (9CI) is a chemical compound that belongs to the amino acid group. It is also known as allyl proline and has a molecular formula of C8H13NO2. L-Proline, 2-(2-propenyl)- (9CI) is typically used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has also been studied for its potential use in the development of novel materials and as a precursor in organic chemistry. L-Proline, 2-(2-propenyl)- (9CI) can also be found in certain foods and has been investigated for its potential health benefits. Overall, it is a versatile and important chemical with a wide range of applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 121772-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,7 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 121772-98:
(8*1)+(7*2)+(6*1)+(5*7)+(4*7)+(3*2)+(2*9)+(1*8)=123
123 % 10 = 3
So 121772-98-3 is a valid CAS Registry Number.

121772-98-3SDS

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 2-Allyl-L-proline

1.2 Other means of identification

Product number -
Other names Boc-|A-allyl-L-proline

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:121772-98-3 SDS

121772-98-3Relevant articles and documents

An improved method of oxazolidinone hydrolysis in the asymmetric synthesis of α-alkylprolines

Genin, Michael J.,Baures, Paul W.,Johnson, Rodney L.

, p. 4967 - 4968 (1994)

An improvement in Seebach's method for the synthesis of α-alkylprolines is reported wherein the hydrolysis of the chiral oxazolidinone 2 is performed on a suspension of silica gel in MeOH/H2O. Following hydrolysis, the pure α-alkylproline can be obtained by filtration thereby avoiding a tedious ion exchange purification.

Design, synthesis, and biological evaluation of new monoamine reuptake inhibitors with potential therapeutic utility in depression and pain

Lucas, Matthew C.,Weikert, Robert J.,Carter, David S.,Cai, Hai-Ying,Greenhouse, Robert,Iyer, Pravin S.,Lin, Clara J.,Lee, Eun Kyung,Madera, Ann Marie,Moore, Amy,Ozboya, Kerem,Schoenfeld, Ryan C.,Steiner, Sandra,Zhai, Yansheng,Lynch, Stephen M.

scheme or table, p. 5559 - 5566 (2011/02/22)

Two new series of monoamine triple reuptake inhibitors (TRIs) have been discovered through scaffold homologation of our recently reported series of 3,3-disubstituted pyrrolidine TRIs. The regioisomeric 2- and 3-ketopyrrolidines demonstrated high levels of

Allosteric modulation of the dopamine receptor by conformationally constrained type VI β-turn peptidomimetics of Pro-Leu-Gly-NH2

Vartak, Ashish P.,Skoblenick, Kevin,Thomas, Nancy,Mishra, Ram K.,Johnson, Rodney L.

, p. 6725 - 6729 (2008/09/17)

A peptidomimetic of Pro-Leu-Pro-NH2, 7, possessing an indolizidinone type VI β-turn mimic was synthesized via improved high-yielding protocols for the preparation and Cbz protection of α-allylproline. Bicyclic peptidomimetic 7 and spirobicylic

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