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132622-69-6

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  • High quality (2r,4r)-4-amino-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid supplier in China

    Cas No: 132622-69-6

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132622-69-6 Usage

General Description

(2S,4R)-1-BOC-4-AMINO-PYRROLIDINE-2-CARBOXYLIC ACID is a chemical compound with the molecular formula C11H18N2O4. It is a derivative of pyrrolidine, a five-membered heterocyclic organic compound containing a nitrogen atom. The compound contains a BOC (tert-butyloxycarbonyl) protecting group, which is commonly used in organic synthesis to protect amine groups from unwanted side reactions. The presence of an amino group in the compound makes it suitable for use in peptide synthesis and as a building block for pharmaceutical agents. It also has potential applications in medicinal chemistry and drug discovery. The (2S,4R) stereochemistry in the compound indicates the arrangement of substituents around the chiral centers in the molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 132622-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,6,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132622-69:
(8*1)+(7*3)+(6*2)+(5*6)+(4*2)+(3*2)+(2*6)+(1*9)=106
106 % 10 = 6
So 132622-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H18N2O4/c1-10(2,3)16-9(15)12-5-6(11)4-7(12)8(13)14/h6-7H,4-5,11H2,1-3H3,(H,13,14)/t6-,7+/m1/s1

132622-69-6SDS

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 (2S,4R)-1-Boc-4-aminopyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names (2S,4R)-4-amino-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid

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:132622-69-6 SDS

132622-69-6Relevant articles and documents

Structure - Activity relationship studies of targeting ligands against breast cancer cells

Yao, Nianhuan,Xiao, Wenwu,Meza, Leah,Tseng, Harry,Chuck, Mathida,Lam, Kit S.

supporting information; experimental part, p. 6744 - 6751 (2010/04/04)

A series of LXY3 (1) analogues were designed and synthesized. Their binding affinity was demonstrated using MDA-MB-231 breast cancer cells adherence inhibition assay. Further structure-activity relationship was obtained. Analogue 29 was discovered to have 3.5-fold increase of the binding affinity. Fluorescent microscopy and in vivo and ex vivo imaging studies demonstrated that 29 is an efficient in vivo targeting agent against α3 integrin of MDA-MB-231 breast tumor xenograft implant. 2009 American Chemical Society.

Inhibitors of Hepatitis C Virus

-

Page/Page column 78-79, (2008/12/04)

Macrocyclic peptides are disclosed having the general formula: wherein R3, R′3, R4, R6, R′, X, Q and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

Hepatitis C virus inhibitors

-

Page/Page column 81, (2010/11/26)

Macrocyclic peptides are disclosed having the general formula: wherein R′, R3, R3′, R4, R6, X, Q, and W are described. Compositions comprising the compounds and methods for using the compounds to inhibit HCV are also disclosed.

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