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4-Bromophenylalanine Hydrochloride Salt is a chemically synthesized compound derived from phenylalanine, an essential amino acid. It has a bromine substituent at the fourth position of the benzene ring, giving it its name. 4-Bromophenylalanine Hydrochloride Salt is often used in scientific research, particularly in the field of biochemistry and molecular biology, as a building block for more complex molecules. On its own, it showcases unique properties due to the presence of a bromine atom, which can be used in a variety of reactions. As a hydrochloride salt, it is typically in a white or off-white crystalline powder form and is highly soluble in water. Its properties, such as melting point, boiling point, or toxicity, may vary depending on the exact composition or the presence of other chemicals.

122839-59-2

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122839-59-2 Usage

Uses

Used in Scientific Research:
4-Bromophenylalanine Hydrochloride Salt is used as a research compound for its unique properties and reactivity in various chemical reactions. Its presence of a bromine atom allows for a wide range of applications in biochemistry and molecular biology.
Used in Biochemistry:
4-Bromophenylalanine Hydrochloride Salt is used as a building block for more complex molecules, contributing to the development of new compounds and understanding of molecular structures.
Used in Molecular Biology:
4-Bromophenylalanine Hydrochloride Salt is used as a component in the synthesis of biologically active molecules, aiding in the study of biological processes and the development of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 122839-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,3 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122839-59:
(8*1)+(7*2)+(6*2)+(5*8)+(4*3)+(3*9)+(2*5)+(1*9)=132
132 % 10 = 2
So 122839-59-2 is a valid CAS Registry Number.

122839-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-amino-3-(4-bromophenyl)propanoic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-2-amino-3-(4-bromophenyl)propanoic acid hydrochloride

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:122839-59-2 SDS

122839-59-2Downstream Products

122839-59-2Relevant academic research and scientific papers

DUAL-ACTING OXAZOLE ANTIHYPERTENSIVE AGENTS

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Page/Page column 23, (2011/02/18)

In one aspect, the invention relates to compounds having the formula: wherein: Ar, Z, R3, R4 and R5 are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds have AT1 re

Generation of N-Methyl-D-aspartate Agonist and Competitive Antagonist Pharmacophore Models. Design and Synthesis of Phosphonoalkyl-Substituted Tetrahydroisoquinolines as Novel Antagonists

Ortwine, Daniel F.,Malone, Thomas C.,Bigge, Christopher F.,Drummond, James T.,Humblet, Christine,et al.

, p. 1345 - 1370 (2007/10/02)

The preparation and binding affinity of a series of tetrahydroisoquinoline carboxylic acids at the N-methyl-D-aspartate (NMDA) subtype of the glutamate receptor is described, together with a molecular modeling analysis of NMDA agonists and antagonists.Usi

Synthesis and antitumor activity of platinum(II) complexes containing substituted ethylenediamine ligands

Brunner, Henri,Hankofer, Peter,Holzinger, Ulrich,Treittinger, Barbara,Schoenenberger, Helmut

, p. 35 - 44 (2007/10/02)

The synthesis of substituted ethylenediamines, their reactions with K2PtCl4 to give the dichloroplatinum(II) complexes, and the exchange of the chloro ligands for other leaving groups are described.The new compounds have been tested as antitumor agents both in vitro using the hormone independent human mammary carcinoma cell line MDA-MB 231 as well as in vivo using the lymphocytic P388 leukemia of the CD2F1-mouse.In the P388 test, 53 of the 55 tested complexes fulfill the minimum activity of 125percent T/C required for a substance to be active.

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