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183860-46-0

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  • 3-[[(4R,5S,6S,7R)-4,7-DIBENZYL-5,6-DIHYDROXY-2-OXO-3-[[3-(2,2,2-TRIFLU OROETHYLCARBAMOYL)PHENYL]METHYL]-1,3-DIAZEPAN-1-YL]METHYL]-N-(2,2,2-TR IFLUOROETHYL)BENZAMIDE

    Cas No: 183860-46-0

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183860-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183860-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,8,6 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 183860-46:
(8*1)+(7*8)+(6*3)+(5*8)+(4*6)+(3*0)+(2*4)+(1*6)=160
160 % 10 = 0
So 183860-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C39H38F6N4O5/c40-38(41,42)23-46-35(52)29-15-7-13-27(17-29)21-48-31(19-25-9-3-1-4-10-25)33(50)34(51)32(20-26-11-5-2-6-12-26)49(37(48)54)22-28-14-8-16-30(18-28)36(53)47-24-39(43,44)45/h1-18,31-34,50-51H,19-24H2,(H,46,52)(H,47,53)/t31-,32-,33+,34+/m1/s1

183860-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-2-oxo-3-[[3-(2,2,2-trifluoroethylcarbamoyl)phenyl]methyl]-1,3-diazepan-1-yl]methyl]-N-(2,2,2-trifluoroethyl)benzamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:183860-46-0 SDS

183860-46-0Downstream Products

183860-46-0Relevant articles and documents

HIV protease inhibitory bis-benzamide cyclic ureas: A quantitative structure-activity relationship analysis

Wilkerson, Wendell W.,Akamike, Emeka,Cheatham, Walter W.,Hollis, Andrea Y.,Collins, R. Dale,DeLucca, Indawati,Lam, Patrick Y. S.,Ru, Yu

, p. 4299 - 4312 (2007/10/03)

A series of N,N'-disubstituted cyclic urea 3-benzamides has been synthesized and evaluated for HIV protease inhibition and antiviral activity. Some of these benzamides have been shown to be potent inhibitors of HIV protease with K(i) 90 20 nM for viral replication and, as such, may be useful in the treatment of AIDS. The synthesis and quantitative structure activity relationship for this benzamide series will be discussed.

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