26086-41-9 Usage
Uses
Used in Chemical Research:
H-HIS(BZL)-OH is utilized as a research compound for studying the interactions and reactions involving histidine and benzyl groups. Its unique structure allows scientists to explore new chemical pathways and mechanisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, H-HIS(BZL)-OH is employed as a building block or a modifying agent for the development of novel drugs. Its potential to influence biological activity makes it a promising candidate for creating new therapeutic agents.
Used in Biochemical Applications:
H-HIS(BZL)-OH serves as a key component in biochemical processes, where it can be used to modulate enzyme activity or to study the effects of histidine-containing peptides and proteins.
Used in Industrial Processes:
H-HIS(BZL)-OH may also find applications in various industrial processes, where its chemical properties can be harnessed for specific technical advancements or improvements.
Given the diverse potential applications of H-HIS(BZL)-OH, its specific uses will depend on the context and the goals of the research or development being pursued.
Check Digit Verification of cas no
The CAS Registry Mumber 26086-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26086-41:
(7*2)+(6*6)+(5*0)+(4*8)+(3*6)+(2*4)+(1*1)=109
109 % 10 = 9
So 26086-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H15N3O2/c14-12(13(17)18)6-11-7-15-9-16(11)8-10-4-2-1-3-5-10/h1-5,7,9,12H,6,8,14H2,(H,17,18)/t12-/m0/s1
26086-41-9Relevant academic research and scientific papers
Regiospecific Synthesis of 3-Substituted L-Histidines
Hodges, John C.
, p. 20 - 24 (2007/10/02)
3-Substituted L-histidine derivatives were prepared by a regiospecific alkylation of N,1-bis-Boc-L-histidine methyl ester with in situ-generated alkyl triflates, benzyl triflates, and benzyl mesylates.Subsequent acid hydrolysis of N-Boc and methyl ester p
