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167824-58-0

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  • 2H-1,3-DAZEPIN-2-ONE,HEXAHYDRO-5,6-DIHYDROXY-1-(5-HYDROXYPENTYL)-3-[(3-HYDROXYPHENYL)METHYL]-4,7-BIS(PHENYLMETHYL)-,(4R,5S,6S,7R)-

    Cas No: 167824-58-0

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167824-58-0 Usage

Description

(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(3-hydroxybenzyl)-3-(5-hydroxypentyl)-1,3-diazepan-2-one is a complex organic molecule characterized by its diazepan ring structure and the presence of multiple hydroxyl groups, making it a polyhydroxy compound. It also features a benzyl group, a 3-hydroxybenzyl group, and a 5-hydroxypentyl group, which contribute to its overall structure and reactivity. The unique combination of functional groups in this compound suggests potential applications in medicinal chemistry, drug design, and chemical synthesis. However, its complex structure also presents challenges in synthesis and characterization.

Uses

Used in Pharmaceutical Industry:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(3-hydroxybenzyl)-3-(5-hydroxypentyl)-1,3-diazepan-2-one is used as a potential pharmaceutical candidate for various applications due to its complex structure and the presence of multiple functional groups. These groups may allow for interactions with biopolymers and macromolecules, making it a promising compound for the development of new drugs.
Used in Drug Design:
In the field of drug design, (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(3-hydroxybenzyl)-3-(5-hydroxypentyl)-1,3-diazepan-2-one is used as a structural template for the development of new molecules with specific biological activities. Its unique combination of functional groups can be exploited to design drugs that target specific receptors or enzymes, potentially leading to more effective treatments for various diseases.
Used in Chemical Synthesis:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(3-hydroxybenzyl)-3-(5-hydroxypentyl)-1,3-diazepan-2-one is used as a synthetic intermediate or building block in the synthesis of other complex organic molecules. Its multiple hydroxyl groups and other functional groups can be used in various chemical reactions to create a wide range of compounds with different properties and applications.
Note: The provided materials do not specify any particular application for (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(3-hydroxybenzyl)-3-(5-hydroxypentyl)-1,3-diazepan-2-one. The uses listed above are inferred based on the general properties of complex organic molecules with multiple functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 167824-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,8,2 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 167824-58:
(8*1)+(7*6)+(6*7)+(5*8)+(4*2)+(3*4)+(2*5)+(1*8)=170
170 % 10 = 0
So 167824-58-0 is a valid CAS Registry Number.

167824-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(5-hydroxypentyl)-3-[(3-hydroxyphenyl)methyl]-1,3-diazepan-2-one

1.2 Other means of identification

Product number -
Other names 2H-1,3-Dazepin-2-one,hexahydro-5,6-dihydroxy-1-(5-hydroxypentyl)-3-((3-hydroxyphenyl)methyl)-4,7-bis(phenylmethyl)-,(4R,5S,6S,7R)

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:167824-58-0 SDS

167824-58-0Downstream Products

167824-58-0Relevant articles and documents

Functionalized aliphatic P2/P2' analogs of HIV-1 protease inhibitor DMP323

Smallheer, Joanne M.,McHugh, Robert J.,Chang, Chong-Hwan,Kaltenbach III, Robert F.,Worley, Tabitha V.,Klabe, Ronald M.,Bacheler, Lee T.,Rayner, Marlene M.,Erickson-Viitanen, Susan,Seitz, Steven P.

, p. 1365 - 1370 (2007/10/03)

A series of analogs of HIV protease inhibitor DMP323 containing functionalized aliphatic P2/P2' groups was prepared and evaluated for HIV protease inhibition and antiviral activity in a cell-based assay. Asymmetric compounds with a 5-hydroxypentyl substituent at P2 and a benzylic substituent at P2' showed increased potency over the corresponding symmetrically substituted analogs.

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