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(2R)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid is a butanoic acid derivative characterized by the presence of an amino group and two carbonyl groups. It features a chirality center at the second carbon, which gives it the (2R) configuration. (2R)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid also includes a phenyl group and a dimethylethoxy group attached to the amino and carboxyl groups, respectively. Its unique structure and functional groups may endow it with potential applications in pharmaceutical or biochemical fields. Careful handling and adherence to safety guidelines are essential due to its potential reactivity and chemical properties.

214852-60-5

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214852-60-5 Usage

Uses

Used in Pharmaceutical Industry:
(2R)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid is used as a potential pharmaceutical compound for its unique structure and functional groups, which may contribute to the development of new drugs or therapeutic agents.
Used in Biochemical Research:
In biochemical research, (2R)-4-[[(1,1-Dimethylethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid can be utilized as a building block or a component in the synthesis of more complex molecules, facilitating the study of biological processes and the development of novel biochemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 214852-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,8,5 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214852-60:
(8*2)+(7*1)+(6*4)+(5*8)+(4*5)+(3*2)+(2*6)+(1*0)=125
125 % 10 = 5
So 214852-60-5 is a valid CAS Registry Number.
InChI:InChI=1S/C17H24N2O6/c1-17(2,3)25-15(22)18-10-9-13(14(20)21)19-16(23)24-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,19,23)(H,20,21)/t13-/m1/s1

214852-60-5SDS

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 2-benzyloxycarbonylamino-4-tert-butoxycarbonylamino-butyric acid

1.2 Other means of identification

Product number -
Other names (2R)-4-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(phenylmethoxycarbonylamino)butanoic 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:214852-60-5 SDS

214852-60-5Relevant academic research and scientific papers

Exploratory solid-phase synthesis of factor Xa inhibitors: Discovery and application of P3-heterocyclic amides as novel types of non-basic arginine surrogates

Ho, Jonathan Z.,Levy, Odile E.,Gibson, Tony S.,Nguyen, Khanh,Semple, J. Edward

, p. 3459 - 3464 (2007/10/03)

A series of novel FXa inhibitors 2a-m and 3a-f was discovered that feature heterocyclic carboxamides tethered to a d-diaminobutyric acid sidechain. These neutral amide derivatives serve as novel P3 d-arginine mimics. Pyrazine carboxamide scaffolds afforded the most potent FXa inhibitors (e.g., 2b IC50 = 4.6 nM). The synthesis and biological activity of two focused libraries are reported.

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