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120108-63-6

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120108-63-6 Usage

General Description

2-Chlorophenylalanine hydrochloride is a chemical compound derived from phenylalanine that has a chlorine atom substituted at the 2-position. It is typically found in a crystalline form and is soluble in water. 2-Chlorophenylalanine hydrochloride is commonly used in pharmaceutical research and development as a building block for the synthesis of novel drugs and for studying the effects of halogen substitution on phenylalanine metabolism. Additionally, 2-Chlorophenylalanine hydrochloride has been researched for its potential use as a therapy for conditions such as depression, anxiety, and other mood disorders, due to its ability to modulate neurotransmitter levels in the brain.

Check Digit Verification of cas no

The CAS Registry Mumber 120108-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,1,0 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120108-63:
(8*1)+(7*2)+(6*0)+(5*1)+(4*0)+(3*8)+(2*6)+(1*3)=66
66 % 10 = 6
So 120108-63-6 is a valid CAS Registry Number.

120108-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-3-(2-chlorophenyl)propanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Chlor-phenylalanin,Hydrochlorid

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:120108-63-6 SDS

120108-63-6Downstream Products

120108-63-6Relevant articles and documents

Anthranilic acid based CCK1 receptor antagonists: Preliminary investigation on their second "touch point"

Varnavas, Antonio,Lassiani, Lucia,Valenta, Valentina,Mennuni, Laura,Makovec, Francesco,Hadjipavlou-Litina, Dimitra

, p. 563 - 581 (2007/10/03)

In this phase of structure-affinity relationship study of VL-0395, a new anthranilic acid based CCK1 selective antagonist, we propose a series of unnatural aminoacidic derivatives. The result of this work is the identification of a new CCK ligand, which possesses an affinity (IC50 = 35 nm) one order of magnitude greater than the lead and, as a general rule, it points out how the hypothesized receptorial pocket which accommodates the Phe residue allows much more structural modification than that interacting with the N-terminal group. Hence, the modification of the C-terminal pharmacophoric group of our lead VL-0395 can not only enhance the affinity of anthranilic acid derivatives but can modulate the selectivity for one CCK receptor subtype or afford mixed antagonists.

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