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Urea, N-[(1R,2R)-2-(dimethylamino)cyclohexyl]-N'-(2,4,6-trimethylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849024-91-5

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849024-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849024-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 849024-91:
(8*8)+(7*4)+(6*9)+(5*0)+(4*2)+(3*4)+(2*9)+(1*1)=185
185 % 10 = 5
So 849024-91-5 is a valid CAS Registry Number.

849024-91-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-{(1R,2R)-2-(dimethylamino)cyclohexyl}-3-mesitylurea

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:849024-91-5 SDS

849024-91-5Downstream Products

849024-91-5Relevant academic research and scientific papers

Structural optimization of thiourea-based bifunctional organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones

Berkessel, Albrecht,Mukherjee, Santanu,Mueller, Thomas N.,Cleemann, Felix,Roland, Katrin,Brandenburg, Marc,Neudoerfl, Joerg-M.,Lex, Johann

, p. 4319 - 4330 (2008/09/18)

This article describes the synthesis of a library of structurally diverse bifunctional organocatalysts bearing both a quasi-Lewis acidic (thio)urea moiety and a Bronsted basic tertiary amine group. Sequential modification of the modular catalyst structure and subsequent screening of the compounds in the alcoholytic dynamic kinetic resolution (DKR) of azlactones revealed valuable structure-activity relationships. In particular, a "hit-structure" was identified which provides e.g. N-benzoyl-tert-leucine allyl ester in an excellent enantiomeric excess of 95%. The Royal Society of Chemistry 2006.

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