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(S)-2-[BENZYL-(3-CHLORO-2-HYDROXY-PROPYL)-AMINO]-N-(4-BENZYLOXY-PHENYL)-ACETAMIDE is a complex organic compound with a unique structure that features a benzyl group attached to an amino group, a chloro and hydroxy group on a propyl chain, a benzyloxy group attached to a phenyl ring, and an acetamide functional group. (S)-2-[BENZYL-(3-CHLORO-2-HYDROXY-PROPYL)-AMINO]-N-(4-BENZYLOXY-PHENYL)-ACETAMIDE has potential pharmaceutical applications due to its distinct structural features and properties.

777934-41-5

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777934-41-5 Usage

Uses

Used in Pharmaceutical Industry:
(S)-2-[BENZYL-(3-CHLORO-2-HYDROXY-PROPYL)-AMINO]-N-(4-BENZYLOXY-PHENYL)-ACETAMIDE is used as a pharmaceutical candidate for various applications due to its unique structure and properties. Its multiple functional groups and complex nature make it a promising compound for the development of new drugs and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 777934-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,7,9,3 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 777934-41:
(8*7)+(7*7)+(6*7)+(5*9)+(4*3)+(3*4)+(2*4)+(1*1)=225
225 % 10 = 5
So 777934-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C25H27ClN2O3/c26-15-23(29)17-28(16-20-7-3-1-4-8-20)18-25(30)27-22-11-13-24(14-12-22)31-19-21-9-5-2-6-10-21/h1-14,23,29H,15-19H2,(H,27,30)/t23-/m1/s1

777934-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[benzyl-[(2S)-3-chloro-2-hydroxypropyl]amino]-N-(4-phenylmethoxyphenyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide,2-[[(2S)-3-chloro-2-hydroxypropyl](phenylmethyl)amino]-N-[4-(phenylmethoxy)phenyl]

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:777934-41-5 SDS

777934-41-5Relevant academic research and scientific papers

Practical synthesis of 1-aryl-6-(hydroxymethyl)-2-ketopiperazines via a 6-exo amide-epoxide cyclization

Powell, Noel A.,Ciske, Fred L.,Clay, Emma C.,Cody, Wayne L.,Downing, Dennis M.,Blazecka, Peter G.,Holsworth, Daniel D.,Edmunds, Jeremy J.

, p. 4069 - 4072 (2007/10/03)

(Chemical Equation Presented) Chiral 1-aryl-6-(hydroxymethyl)-2- ketopiperazines can be prepared via an operationally simple, 6-exo epoxide ring-opening cyclization to form the ketopiperazine C6-N1 bond in high yields and with excellent enantiomeric purity.

PIPERAZINE DERIVATIVE RENIN INHIBITORS

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Page 59; 61, (2010/02/09)

Disclosed are piperazine derivatives, their manufacture and use as inhibitors of renin. Formula (I):

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