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111119-37-0

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111119-37-0 Usage

General Description

L-2,6-Dichlorophenylalanine is a synthetic compound derived from the amino acid phenylalanine. It is characterized by its two chlorine atoms at 2nd and 6th position in the phenyl ring of phenylalanine. Due to its highly active nature, it is commonly used in scientific research, including studies involving protein synthesis and enzyme activity. Its chemical and structural properties also make it a subject of interest in the production of certain pharmaceuticals, including potential use as an antibiotic or anticancer agent. It is not naturally occurring and needs to be synthesized in a lab setting. As with many chemicals, it should be handled with care due to potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 111119-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,1 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111119-37:
(8*1)+(7*1)+(6*1)+(5*1)+(4*1)+(3*9)+(2*3)+(1*7)=70
70 % 10 = 0
So 111119-37-0 is a valid CAS Registry Number.

111119-37-0SDS

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 (S)-2-Amino-3-(2,6-dichlorophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names (2S)-2-amino-3-(2,6-dichlorophenyl)propanoic 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:111119-37-0 SDS

111119-37-0Upstream product

111119-37-0Downstream Products

111119-37-0Relevant 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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