56217-34-6 Usage
Description
H-Har-OMe.2HCL is a chemical compound that consists of the amino acid Har-OMe and two molecules of hydrochloric acid. Har-OMe is a derivative of the amino acid histidine, which is commonly found in proteins and has various biological functions. The addition of hydrochloric acid to Har-OMe can alter its chemical properties, making it more water-soluble and suitable for specific research or industrial applications.
Uses
Used in Pharmaceutical Research:
H-Har-OMe.2HCL is used as a research compound for studying the properties and functions of histidine and its derivatives. It aids in understanding the role of histidine in biological processes and the development of new pharmaceutical agents.
Used in Chemical Synthesis:
H-Har-OMe.2HCL is used as a reagent in chemical synthesis, particularly in the production of other histidine derivatives or related compounds. Its water-solubility and altered chemical properties make it a useful component in various organic chemistry reactions.
Used in Organic Chemistry Reactions:
H-Har-OMe.2HCL is used as a reactant in organic chemistry reactions, where its unique properties can contribute to the synthesis of new compounds or the modification of existing ones. Its versatility in chemical reactions makes it a valuable tool for researchers in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 56217-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56217-34:
(7*5)+(6*6)+(5*2)+(4*1)+(3*7)+(2*3)+(1*4)=116
116 % 10 = 6
So 56217-34-6 is a valid CAS Registry Number.
56217-34-6Relevant articles and documents
Studies on analgesic oligopeptides. II. Structure-activity relationship among thirty analogs of a cyclic dipeptide, cyclo(-Tyr-Arg-)
Sasaki,Akutsu,Matsui,Suzuki,Sakurada,Sato,Kisara
, p. 4435 - 4443 (2007/10/02)
Thirty diketopiperazines were synthesized as analogs of cyclo(-Tyr-Arg-). The analgesic activities of these analogs were evaluated after intracerebral administration in mice. In the cyclo(-X-Arg-) series of analogs, cyclo[-Tyr(Et)-Arg-] showed the most po
