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1174913-73-5

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1174913-73-5 Usage

General Description

(S)-2-N-Cbz-aminomethylmorpholine is a chemical compound that is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds. It is a derivative of morpholine, a heterocyclic amine, and its structure includes a carbobenzyloxy (Cbz) group attached to the amino group. (S)-2-N-Cbz-aminomethylmorpholine is important in organic and medicinal chemistry as it can be used to introduce the morpholine moiety into various molecules, with the potential to modulate biological activity. The (S)-2-N-Cbz-aminomethylmorpholine is characterized by its ability to act as a nucleophile and a ligand in metal-catalyzed reactions, making it versatile for use in a wide range of chemical transformations.

Check Digit Verification of cas no

The CAS Registry Mumber 1174913-73-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,9,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1174913-73:
(9*1)+(8*1)+(7*7)+(6*4)+(5*9)+(4*1)+(3*3)+(2*7)+(1*3)=165
165 % 10 = 5
So 1174913-73-5 is a valid CAS Registry Number.

1174913-73-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[[(2S)-morpholin-2-yl]methyl]carbamate

1.2 Other means of identification

Product number -
Other names FC0046

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:1174913-73-5 SDS

1174913-73-5Relevant articles and documents

Identification of inhibitors of checkpoint kinase 1 through template screening

Matthews, Thomas P.,Klair, Suki,Burns, Samantha,Boxall, Kathy,Cherry, Michael,Fisher, Martin,Westwood, Isaac M.,Walton, Michael I.,McHardy, Tatiana,Cheung, Kwai-Ming J.,Van Montfort, Rob,Williams, David,Aherne, G. Wynne,Garrett, Michelle D.,Reader, John,Collins, Ian

supporting information; experimental part, p. 4810 - 4819 (2010/03/01)

Checkpoint kinase 1 (CHK1) is an oncology target of significant current interest. Inhibition of CHK1 abrogates DNA damage-induced cell cycle checkpoints and sensitizes p53 deficient cancer cells to genotoxic therapies. Using template screening, a fragment

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