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269398-80-3

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269398-80-3 Usage

General Description

BOC-(R)-3-AMINO-4-(2-METHYL-PHENYL)-BUTYRIC ACID, also known as (R)-2-(tert-butoxycarbonylamino)-3-methyl-4-phenylbutanoic acid, is a compound used in the field of organic chemistry. It is a chiral compound with a BOC (tert-butoxycarbonyl) protecting group and an amino acid functional group, making it useful in peptide synthesis and pharmaceutical research. This chemical may also have potential applications in the development of new drugs and pharmaceuticals due to its unique properties and structure.

Check Digit Verification of cas no

The CAS Registry Mumber 269398-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,3,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 269398-80:
(8*2)+(7*6)+(6*9)+(5*3)+(4*9)+(3*8)+(2*8)+(1*0)=203
203 % 10 = 3
So 269398-80-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H23NO4/c1-11-7-5-6-8-12(11)9-13(10-14(18)19)17-15(20)21-16(2,3)4/h5-8,13H,9-10H2,1-4H3,(H,17,20)(H,18,19)/t13-/m1/s1

269398-80-3SDS

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 Boc-(R)-3-amino-4-(2-methylphenyl)-butyric acid

1.2 Other means of identification

Product number -
Other names RARECHEM AK PT B060

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:269398-80-3 SDS

269398-80-3Downstream Products

269398-80-3Relevant articles and documents

Discovery of potent and selective β-homophenylalanine based dipeptidyl peptidase IV inhibitors

Xu, Jinyou,Ok, Hyun O.,Gonzalez, Edward J.,Colwell Jr., Lawrence F.,Habulihaz, Bahanu,He, Huaibing,Leiting, Barbara,Lyons, Kathryn A.,Marsilio, Frank,Patel, Reshma A.,Wu, Joseph K.,Thornberry, Nancy A.,Weber, Ann E.,Parmee, Emma R.

, p. 4759 - 4762 (2007/10/03)

Modification of in-house screening lead β-aminoacyl proline 8 gave an equipotent thiazolidide 9. Extensive SAR studies on the phenyl ring of 9 led to the discovery of a novel series of potent and selective DP-IV inhibitors. Introduction of a fluorine at the 2-position proved to be crucial for the potency of this series. The 2,5-difluoro (22q) and 2,4,5-trifluoro (22t) analogues were potent inhibitors of DP-IV (IC50 = 270, 119 nM, respectively).

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