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Carbamic acid, [(1S)-1-formylpentyl]-, (1S)-1-methyl-2-phenylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

736144-17-5

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736144-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736144-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,1,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 736144-17:
(8*7)+(7*3)+(6*6)+(5*1)+(4*4)+(3*4)+(2*1)+(1*7)=155
155 % 10 = 5
So 736144-17-5 is a valid CAS Registry Number.

736144-17-5SDS

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 [(2S)-1-phenylpropan-2-yl] N-[(2S)-1-oxohexan-2-yl]carbamate

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:736144-17-5 SDS

736144-17-5Downstream Products

736144-17-5Relevant academic research and scientific papers

Exploration of the P2-P3 SAR of aldehyde cathepsin K inhibitors

Boros, Eric E.,Deaton, David N.,Hassell, Anne M.,McFadyen, Robert B.,Miller, Aaron B.,Miller, Larry R.,Paulick, Margot G.,Shewchuk, Lisa M.,Thompson, James B.,Willard Jr., Derril H.,Wright, Lois L.

, p. 3425 - 3429 (2007/10/03)

The synthesis and biological activity of a series of aldehyde inhibitors of cathepsin K are reported. Exploration of the properties of the S2 and S3 subsites with a series of carbamate derivatized norleucine aldehydes substituted at the P2 and P3 positions afforded analogs with cathepsin K IC50s between 600nM and 130pM.

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