16652-64-5 Usage
Description
H-TYR(BZL)-OH, also known as O-Benzyl-L-tyrosine, is a crystalline compound that serves as a substrate for aminotransferases, specifically PAT3. It is a derivative of the amino acid tyrosine, with a benzyl group attached to the hydroxyl group, which influences its chemical properties and reactivity.
Uses
Used in Biochemical Research:
H-TYR(BZL)-OH is used as a substrate in biochemical research for studying the activity and function of aminotransferases, particularly PAT3. Its unique structure allows researchers to investigate enzyme kinetics, mechanism, and specificity.
Used in Pharmaceutical Development:
In the pharmaceutical industry, H-TYR(BZL)-OH can be utilized as an intermediate or building block in the synthesis of various drugs and bioactive compounds. Its reactivity and structural features make it a valuable component in medicinal chemistry.
Used in Analytical Chemistry:
H-TYR(BZL)-OH can be employed as a reference compound or standard in analytical chemistry for the development and validation of methods for the detection, quantification, and analysis of related compounds in complex samples.
Used in Organic Synthesis:
Due to its unique structure, H-TYR(BZL)-OH can be used as a starting material or reactant in organic synthesis for the preparation of a variety of organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 16652-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,5 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16652-64:
(7*1)+(6*6)+(5*6)+(4*5)+(3*2)+(2*6)+(1*4)=115
115 % 10 = 5
So 16652-64-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO3/c17-15(16(18)19)10-12-6-8-14(9-7-12)20-11-13-4-2-1-3-5-13/h1-9,15H,10-11,17H2,(H,18,19)/t15-/m1/s1
16652-64-5Relevant articles and documents
Stereoselective Modification of N-(α-Hydroxyacyl)-glycinesters via Palladium-Catalyzed Allylic Alkylation
Horn, Alexander,Kazmaier, Uli
supporting information, p. 4595 - 4599 (2019/06/27)
N-(α-Hydroxyacyl)-glycinesters can be used as excellent nucleophiles in Pd-catalyzed allylic alkylation. The method allows for the stereoselective introduction of a wide range of side chains, including highly functionalized ones. Both diastereomers can be accessed through variation of the reaction conditions. Furthermore, the use of stannylated carbonates introduces vinylstannane motifs, which are eligible for subsequent C-C coupling reactions.
Synthesis of enantiopure free and N-benzyloxycarbonyl-protected 3-substituted homotaurines from naturally occurring amino acids
Zheng, Yongpeng,Xu, Jiaxi
, p. 5197 - 5206 (2014/07/08)
Enantiopure N-benzyloxycarbonyl-protected and free 3-substituted homotaurines were synthesized from naturally occurring amino acids via N-benzyloxycarbonyl protection, Arndt-Eistert homologation, reduction, esterification with thioacetic acid, and oxidation with performic acid. The current method is a convenient, practical, and salt-free method for the synthesis of enantiopure 3-substituted homotaurine with moderate to good yields.
A PROCESS FOR PREPARATION OF PYRROLES HAVING HYPOLIPIDEMIC HYPOCHOLESTEREMIC ACTIVITIES
-
Page/Page column 27, (2015/01/06)
The present invention provides pyrroles having hypolipidemic hypocholesteremic activities. The invention provides saroglitazar and its pharmaceutically acceptable salts, hydrates, solvates, polymorphs or intermediates thereof. The invention also provides a process for the preparation of saroglitazar. The invention further provides intermediates as well process for preparation thereof.