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167824-57-9

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  • 2H-1,3-DIAZEPIN-2-ONE,HEXAHYDRO-5,6-DIHYDROXY-1-(6-HYDROXYHEXYL)-3-(2-NAPHTHALENYLMETHYL)-4,7-BIS(PHENYLMETHYL)-,(4R,5S,6S,7R)-

    Cas No: 167824-57-9

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  • Hangzhou Fandachem Co.,Ltd
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  • 2H-1,3-Diazepin-2-one,hexahydro-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(2-naphthalenylmethyl)-4,7-bis(phenylmethyl)-,[4R-(4a,5a,6b,7b)]- (9CI)

    Cas No: 167824-57-9

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  • Kingston Chemicals Ltd.
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167824-57-9 Usage

Description

(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one is a complex chiral chemical compound belonging to the diazepane derivatives class. It features a diazepane ring with two hydroxyl groups, a naphthalene-2-ylmethyl group, and a benzyl group, along with four stereocenters. (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one holds promise for pharmaceutical research due to its unique structure and potential biological activities, although further studies are required to determine its pharmacological properties and medical applications.

Uses

Used in Pharmaceutical Research:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one is used as a potential candidate in pharmaceutical research for its unique structure and potential biological activities. (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one's specific stereochemistry and functional groups may offer novel interactions with biological targets, making it a valuable molecule for the development of new therapeutics.
Used in Drug Design and Development:
In the field of drug design and development, (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one can be utilized as a starting point for the creation of new drugs. Its structural features may be exploited to design molecules with improved pharmacokinetic and pharmacodynamic profiles, targeting specific diseases or conditions.
Used in Chemical Synthesis:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one may also find applications in chemical synthesis, where it can serve as an intermediate or a building block for the synthesis of more complex molecules with diverse applications, such as agrochemicals, materials science, or specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 167824-57-9 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 167824-57:
(8*1)+(7*6)+(6*7)+(5*8)+(4*2)+(3*4)+(2*5)+(1*7)=169
169 % 10 = 9
So 167824-57-9 is a valid CAS Registry Number.

167824-57-9SDS

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-(6-hydroxyhexyl)-3-(naphthalen-2-ylmethyl)-1,3-diazepan-2-one

1.2 Other means of identification

Product number -
Other names 2H-1,3-Diazepin-2-one,hexahydro-5,6-dihydroxy-1-(6-hydroxyhexyl)-3-(2-naphthalenylmethyl)-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:167824-57-9 SDS

167824-57-9Downstream Products

167824-57-9Relevant 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 (1997)

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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