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(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one is a complex organic molecule characterized by its diazepane ring structure. It is highly substituted and functionalized, featuring four benzyl groups, two hydroxyl groups, and two 3-methylbutyl groups. The stereochemistry of the molecule is defined by the (4R,5S,6S,7R) designation, which specifies the arrangement of the substituents on the diazepane ring. (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one may hold potential for various applications in medicinal chemistry, organic synthesis, and as a molecular scaffold for the development of new chemical entities.

153181-45-4

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153181-45-4 Usage

Uses

Used in Medicinal Chemistry:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one is used as a molecular scaffold for the development of new pharmaceuticals due to its complex structure and multiple functional groups, which can be exploited for various biological activities.
Used in Organic Synthesis:
In the field of organic synthesis, (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one serves as a versatile intermediate or building block for the synthesis of more complex organic compounds, taking advantage of its multiple reactive sites.
Used in Drug Design:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one is used as a lead compound in drug design for potential therapeutic applications, given its unique stereochemistry and functional groups that may interact with biological targets.

Check Digit Verification of cas no

The CAS Registry Mumber 153181-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,8 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153181-45:
(8*1)+(7*5)+(6*3)+(5*1)+(4*8)+(3*1)+(2*4)+(1*5)=114
114 % 10 = 4
So 153181-45-4 is a valid CAS Registry Number.

153181-45-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(3-methylbutyl)-1,3-diazepan-2-one

1.2 Other means of identification

Product number -
Other names DMPC Cyclic Urea 43

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:153181-45-4 SDS

153181-45-4Downstream Products

153181-45-4Relevant academic research and scientific papers

Cyclic HIV protease inhibitors: Synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas

Lam, Patrick Y. S.,Ru, Yu,Jadhav, Prabhakar K.,Aldrich, Paul E.,DeLucca, George V.,Eyermann, Charles J.,Chang, Chong-Hwan,Emmett, George,Holler, Edward R.,Daneker, Wayne F.,Li, Liangzhu,Confalone, Pat N.,McHugh, Robert J.,Han, Qi,Li, Renhua,Markwalder, Jay A.,Seitz, Steven P.,Sharpe, Thomas R.,Bacheler, Lee T.,Rayner, Marlene M.,Klabe, Ronald M.,Shum, Linyee,Winslow, Dean L.,Kornhauser, David M.,Jackson, David A.,Erickson-Viitanen, Susan,Hodge, C. Nicholas

, p. 3514 - 3525 (2007/10/03)

High-resolution X-ray structures of the complexes of HIV-1 protease (HIV-1PR) with peptidomimetic inhibitors reveal the presence of a structural water molecule which is hydrogen bonded to both the mobile flaps of the enzyme and the two carbonyls flanking

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