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608528-91-2

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608528-91-2 Usage

Description

(S)-3-BIPHENYL-3-YL-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID is a chiral non-proteinogenic amino acid derivative featuring a biphenyl group, a tert-butoxycarbonyl amino group, and a propionic acid moiety. It is an important building block in organic synthesis and pharmaceutical research, particularly for the preparation of peptidomimetics and peptidic drug molecules. Its asymmetric carbon center makes it a valuable component for the synthesis of enantiomerically pure compounds, which is crucial for the development of novel drug candidates and the study of molecular interactions involving amino acid derivatives in biological systems.

Uses

Used in Pharmaceutical Research:
(S)-3-BIPHENYL-3-YL-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID is used as a key building block in the synthesis of peptidomimetics and peptidic drug molecules, contributing to the development of innovative therapeutic agents with improved pharmacological properties.
Used in Organic Synthesis:
As a chiral compound with an asymmetric carbon center, (S)-3-BIPHENYL-3-YL-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID is utilized in the synthesis of enantiomerically pure compounds, which are essential for various applications in the chemical and pharmaceutical industries.
Used in Drug Development:
(S)-3-BIPHENYL-3-YL-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID serves as a valuable component in the development of novel drug candidates, providing a structural foundation for the creation of new therapeutic agents with potential applications in various medical fields.
Used in Molecular Interaction Studies:
(S)-3-BIPHENYL-3-YL-2-TERT-BUTOXYCARBONYLAMINO-PROPIONIC ACID is employed in the study of molecular interactions involving amino acid derivatives, helping researchers understand their effects on biological systems and contributing to the advancement of our knowledge in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 608528-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,8,5,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 608528-91:
(8*6)+(7*0)+(6*8)+(5*5)+(4*2)+(3*8)+(2*9)+(1*1)=172
172 % 10 = 2
So 608528-91-2 is a valid CAS Registry Number.

608528-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(3-phenylphenyl)propanoic acid

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:608528-91-2 SDS

608528-91-2Downstream Products

608528-91-2Relevant articles and documents

Intensified biocatalytic production of enantiomerically pure halophenylalanines from acrylic acids using ammonium carbamate as the ammonia source

Weise, Nicholas J.,Ahmed, Syed T.,Parmeggiani, Fabio,Siirola, Elina,Pushpanath, Ahir,Schell, Ursula,Turner, Nicholas J.

, p. 4086 - 4089 (2016/07/06)

An intensified, industrially-relevant strategy for the production of enantiopure halophenylalanines has been developed using the novel combination of a cyanobacterial phenylalanine ammonia lyase (PAL) and ammonium carbamate reaction buffer. The process boasts STYs up to >200 g L-1 d-1, ees ≥ 98% and simplified catalyst/reaction buffer preparation and work up.

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