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7662-51-3

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7662-51-3 Usage

Description

L-TYROSINE HYDRAZIDE is an organic compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals and chemicals. It is a white crystalline solid and is known for its ability to resolve DL-amino acids, making it a valuable compound in the field of chemistry and pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
L-TYROSINE HYDRAZIDE is used as a resolving agent for various DL-amino acids, playing a significant role in the separation and purification of these essential building blocks of proteins. This application is crucial in the development and production of various pharmaceuticals, as amino acids are the primary constituents of many drugs.
Used in Chemical Research:
L-TYROSINE HYDRAZIDE is used as an excellent reagent for the resolution of amino acids in chemical research. Its ability to resolve DL-amino acids makes it a valuable tool for scientists and researchers working on the development of new drugs and the study of protein structures. This application aids in advancing our understanding of the molecular basis of various diseases and the design of targeted therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 7662-51-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,6 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7662-51:
(6*7)+(5*6)+(4*6)+(3*2)+(2*5)+(1*1)=113
113 % 10 = 3
So 7662-51-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N3O2/c10-8(9(14)12-11)5-6-1-3-7(13)4-2-6/h1-4,8,13H,5,10-11H2,(H,12,14)/p+1/t8-/m0/s1

7662-51-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Aldrich

  • (138045)  L-Tyrosinehydrazide  98%

  • 7662-51-3

  • 138045-1G

  • 223.47CNY

  • Detail
  • Aldrich

  • (138045)  L-Tyrosinehydrazide  98%

  • 7662-51-3

  • 138045-5G

  • 532.35CNY

  • Detail

7662-51-3SDS

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 L-TYROSINE HYDRAZIDE

1.2 Other means of identification

Product number -
Other names H-TYR-NHNH2

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:7662-51-3 SDS

7662-51-3Relevant articles and documents

Dynamic Combinatorial Chemistry to Identify Binders of ThiT, an S-Component of the Energy-Coupling Factor Transporter for Thiamine

Monjas, Leticia,Swier, Lotteke J. Y. M.,Setyawati, Inda,Slotboom, Dirk J.,Hirsch, Anna K. H.

supporting information, p. 1693 - 1696 (2017/10/27)

We applied dynamic combinatorial chemistry (DCC) to identify ligands of ThiT, the S-component of the energy-coupling factor (ECF) transporter for thiamine in Lactococcus lactis. We used a pre-equilibrated dynamic combinatorial library (DCL) and saturation-transfer difference (STD) NMR spectroscopy to identify ligands of ThiT. This is the first report in which DCC is used for fragment growing to an ill-defined pocket, and one of the first reports for its application with an integral membrane protein as target.

Synthesis of novel 1-[(1-ethoxymethylene)amino]imidazol-5(4H)-ones and 1,2,4-triazin-6(5H)-ones from optically active α-aminocarboxylic acid hydrazides

Kudelko, Agnieszka,Zieliński, Wojciech,Jasiak, Karolina

, p. 4637 - 4640 (2013/08/23)

New derivatives of 1-[(1-ethoxymethylene)amino]imidazol-5(4H)-one and 1,2,4-triazin-6(5H)-one were synthesized via reactions of optically active α-aminocarboxylic acid hydrazides and triethyl orthoesters in xylene. The factors influencing the formation of the unexpected five-membered products and attempts to elucidate the mechanism are discussed.

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