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458529-69-6

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458529-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 458529-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,8,5,2 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 458529-69:
(8*4)+(7*5)+(6*8)+(5*5)+(4*2)+(3*9)+(2*6)+(1*9)=196
196 % 10 = 6
So 458529-69-6 is a valid CAS Registry Number.

458529-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl {(1S)-3-[methoxy(methyl)amino]-3-oxo-1-phenylpropyl}carbamate

1.2 Other means of identification

Product number -
Other names (S)-N-methyl-N-methoxy-3-phenyl-3-tert-butoxycarbonylaminopropionamide

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:458529-69-6 SDS

458529-69-6Relevant articles and documents

1-Amido-1-phenyl-3-piperidinylbutanes - CCR5 antagonists for the treatment of HIV: Part 2

Barber, Christopher G.,Blakemore, David C.,Chiva, Jean-Yves,Eastwood, Rachel L.,Middleton, Donald S.,Paradowski, Kerry A.

scheme or table, p. 1499 - 1503 (2009/12/07)

Optimisation of a series of 4-piperidinyltriazoles led to the identification of compound 28a which showed good whole cell antiviral activity, excellent selectivity over the hERG ion channel and complete oral absorption.

TRIAZOLYLPIPERIDINE DERIVATIVES AND USE THEREOF IN THERAPY

-

, (2010/11/25)

The present invention provides compounds of formula (I) Wherein R1 , R2, R3 , R4 , Het and m are as defined in the description. The compounds of the present invention are modulators, especially antagonists, of the activity of chemokine CCR5 receptors.

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