150767-06-9 Usage
Uses
Used in Organic Chemistry:
2-(t-Butyloxycarbonyl)amino-4S-hydroxy-5S-(benzyloxycarbonyl)amino-1,6-diphenyl-2-azahexane is used as a protective agent for [Asparagine and Serine amino acids] in [solid-phase peptide synthesis], allowing for [selective deprotection and subsequent coupling reactions].
Used in Biochemistry:
2-(t-Butyloxycarbonyl)amino-4S-hydroxy-5S-(benzyloxycarbonyl)amino-1,6-diphenyl-2-azahexane is used as a peptide derivative in [the synthesis of complex peptides and proteins], providing [protection and easy removal of protective groups under mild conditions].
Used in Pharmaceutical Applications:
2-(t-Butyloxycarbonyl)amino-4S-hydroxy-5S-(benzyloxycarbonyl)amino-1,6-diphenyl-2-azahexane is used as a key component in [the production and study of peptides and proteins], contributing to [various research and pharmaceutical applications].
Check Digit Verification of cas no
The CAS Registry Mumber 150767-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,7,6 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150767-06:
(8*1)+(7*5)+(6*0)+(5*7)+(4*6)+(3*7)+(2*0)+(1*6)=129
129 % 10 = 9
So 150767-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C30H37N3O5/c1-30(2,3)38-29(36)32-33(20-24-15-9-5-10-16-24)21-27(34)26(19-23-13-7-4-8-14-23)31-28(35)37-22-25-17-11-6-12-18-25/h4-18,26-27,34H,19-22H2,1-3H3,(H,31,35)(H,32,36)/t26-,27-/m0/s1
150767-06-9Relevant academic research and scientific papers
Antiretroviral hydrazine derivatives
-
, (2008/06/13)
The invention relates to compounds of formula STR1 and salts, pharmaceutical compositions, intermediates and processes of preparation thereof.
RETROVIRAL PROTEASE INHIBITING COMPOUNDS
-
, (2008/06/13)
A retroviral protease inhibiting compound of the formula: STR1 is disclosed wherein R 1, R 2, R 5, R 6, Y m and Y' n are herein defined.
Facile Synthesis of Potent HIV-1 Protease Inhibitors containing a Novel Pseudo-symmetric Dipeptide Isostere
Sham, Hing L.,Betebenner, David A.,Zhao, Chen,Wideburg, Norman E.,Saldivar, Ayda,et al.
, p. 1052 - 1053 (2007/10/02)
A series of potent inhibitors of the HIV-1 protease containing a novel pseudo-symmetric dipeptide isostere 3 was synthesized via ring opening of a protected epoxide with various substituted hydrazines.
