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6637-65-6

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6637-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6637-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6637-65:
(6*6)+(5*6)+(4*3)+(3*7)+(2*6)+(1*5)=116
116 % 10 = 6
So 6637-65-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2O2/c1-4-10-6(9)8-7-5(2)3/h5,7H,4H2,1-3H3,(H,8,9)

6637-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(propan-2-ylamino)carbamate

1.2 Other means of identification

Product number -
Other names ethyl 2-(propan-2-yl)hydrazinecarboxylate

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:6637-65-6 SDS

6637-65-6Downstream Products

6637-65-6Relevant articles and documents

The α-effect in iminium ion catalysis

Cavill, Julie L.,Elliott, Richard L.,Evans, Gareth,Jones, Ian L.,Platts, James A.,Ruda, Antonio M.,Tomkinson, Nicholas C. O.

, p. 410 - 421 (2007/10/03)

The α-effect can be used as an effective means to promote iminium ion catalysed transformations, providing acyclic scaffolds to aid in catalyst design. A thorough investigation of the structure-activity relationship of the catalyst architecture reveals optimal substituents of a disubstituted carbamate and a secondary alkyl group around a hydrazine scaffold. Molecular modelling investigations provide a mechanistic rationale to the results observed.

The synthesis of azapeptidomimetic beta-lactam molecules as potential protease inhibitors.

Malachowski, William P,Tie, Chenyang,Wang, Katherine,Broadrup, Robert L

, p. 8962 - 8969 (2007/10/03)

Synthetic methods for the construction of a novel peptidomimetic structure are reported. The structure incorporates a beta-lactam and an azapeptide in a peptide backbone with the intention of generating rationally designed substrate-based protease inhibitors. The beta-lactam is formed by subjecting serine or threonine-azapeptides to Mitsunobu reaction conditions. Importantly, the azapeptidomimetic beta-lactam structure permits extended binding inhibition and the synthetic methods to create tetrapeptidomimetic structures are described.

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