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2-amino-3-(2-bromo-5-hydroxyphenyl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123254-09-1

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123254-09-1 Usage

General Description

2-amino-3-(2-bromo-5-hydroxyphenyl)propanoic acid is a chemical compound with the molecular formula C9H10BrNO3. It is a derivative of the amino acid tyrosine, with a bromine atom and a hydroxyl group attached to the phenyl ring. 2-amino-3-(2-bromo-5-hydroxyphenyl)propanoic acid has potential applications in the field of pharmaceuticals and biotechnology, particularly in the development of drugs targeting specific receptors and enzymes. Its unique structure and properties make it a subject of interest in research related to the synthesis and characterization of new compounds for various medicinal purposes. Additionally, its structure suggests that it may have potential biological activities, making it a promising candidate for further investigation and development.

Check Digit Verification of cas no

The CAS Registry Mumber 123254-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,5 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 123254-09:
(8*1)+(7*2)+(6*3)+(5*2)+(4*5)+(3*4)+(2*0)+(1*9)=91
91 % 10 = 1
So 123254-09-1 is a valid CAS Registry Number.

123254-09-1Upstream product

123254-09-1Downstream Products

123254-09-1Relevant academic research and scientific papers

The scope and limitations of the Suzuki-Miyaura cross-coupling reactions of 6- and 8-substituted 1,2,3,4-tetrahydroisoquinoline-3-carboxylates

McKenna, Jeffrey M.,Moliterni, John,Qiao, Ying

, p. 5797 - 5800 (2001)

6- and 8-Aryl-1,2,3,4-tetrahydroisoqinoline-3-carboxylates have been prepared by Suzuki-Miyaura cross-coupling reactions of the triflates or corresponding boronate esters. We have shown for the first time that a one-pot arylation of a triflate via the bor

COMPOUNDS FOR BINDING PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 9 (PCSK9)

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Paragraph 0364, (2017/09/15)

The present disclosure relates to novel compounds, methods, and compositions capable of binding to PCSK9, thereby modulating PCSK9 proprotein convertase enzyme activity. The compounds of the disclosure include compounds Formula (I).

Discovery of small-molecule nonpeptide antagonists of nociceptin/orphanin FQ receptor: The studies of design, synthesis, and structure-Activity relationships for (4-Arylpiperidine substituted-methyl)-[bicyclic (hetero)cycloalkanobenzene] derivatives

Hayashi, Shigeo,Ohashi, Katsuyo,Mihara, Sachiko,Nakata, Eriko,Emoto, Chie,Ohta, Atsuko

, p. 345 - 364 (2016/04/19)

Nociceptin/orphanin FQ (N/OFQ) and N/OFQ peptide (NOP) receptor are expressed and distributed in various regions such as central nervous system (CNS), peripheral nervous system, immune system, and peripheral tissues. N/OFQ and NOP receptor have important

Substituted Tetrahydroisoquinolines as Beta-secretase Inhibitors

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Page/Page column 20, (2008/12/06)

There is provided a series of tetrahydroisoquinoline diaminopropane compounds of Formula (I) or a stereoisomer; or a pharmaceutically acceptable salt thereof, wherein R, R8 and R9 are as defined herein, their pharmaceutical compositi

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