112157-33-2 Usage
Description
(L-LEUCINETHIOL)2 2 HCL is a chemical compound composed of two molecules of L-leucinethiol and two molecules of hydrogen chloride. L-leucinethiol, a derivative of the amino acid leucine, is utilized in the synthesis of peptides and proteins. The combination with hydrogen chloride results in a salt that can be employed in various chemical reactions and serves as a reagent in organic chemistry. (L-LEUCINETHIOL)2 2 HCL may find applications in the pharmaceutical, biochemistry, and other industries that require amino acid and peptide manipulation.
Uses
Used in Pharmaceutical Industry:
(L-LEUCINETHIOL)2 2 HCL is used as a reagent for the synthesis of peptides and proteins, which are essential components in drug development and pharmaceutical research. Its role in creating and modifying these biological molecules contributes to the advancement of new medications and therapies.
Used in Biochemistry Research:
In the field of biochemistry, (L-LEUCINETHIOL)2 2 HCL is used as a research tool to study the properties and interactions of amino acids, peptides, and proteins. This understanding can lead to insights into various biological processes and the development of targeted treatments for diseases.
Used in Organic Chemistry:
(L-LEUCINETHIOL)2 2 HCL serves as a versatile reagent in organic chemistry, enabling the manipulation of amino acid structures and the formation of new compounds. Its applications in this field can lead to the discovery of novel chemical reactions and the synthesis of innovative materials.
Check Digit Verification of cas no
The CAS Registry Mumber 112157-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,5 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112157-33:
(8*1)+(7*1)+(6*2)+(5*1)+(4*5)+(3*7)+(2*3)+(1*3)=82
82 % 10 = 2
So 112157-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H28N2S2.2ClH/c1-9(2)5-11(13)7-15-16-8-12(14)6-10(3)4;;/h9-12H,5-8,13-14H2,1-4H3;2*1H/t11-,12-;;/m0../s1
112157-33-2Relevant articles and documents
Synthesis of Sulfur-Containing Analogues of Bestatin. Inhibition of Aminopeptidases by α-Thiolbestatin Analogues
Ocain, Timothy D.,Rich, Daniel H.
, p. 2193 - 2199 (2007/10/02)
Sulfur-containing amino acid and peptide analogues of bestatin (1) have been synthesized and evaluated as inhibitors of aminopeptidase M (AP-M), leucine aminopeptidase (LAP), and aminopeptidase B (A
