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N-{1-methyl-1-[3-(1-methylethenyl)phenyl]ethyl}-2-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)acetamide is a complex organic compound with a molecular formula of C27H31N2O. It is a derivative of acetamide, featuring a 1-methyl-1-[3-(1-methylethenyl)phenyl]ethyl group attached to the nitrogen atom, and a 1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene group connected to the carbonyl carbon. N-{1-methyl-1-[3-(1-methylethenyl)phenyl]ethyl}-2-(1,3,3-trimethyl-1,3-dihydro-2H-indol-2-ylidene)acetamide is characterized by its unique structure, which includes a phenyl ring with a methyl group and a vinyl group, an ethyl chain, and an indole ring system with three methyl groups. It is likely to have specific applications in fields such as pharmaceuticals or materials science, where its unique structure could confer particular properties or reactivity.

6538-73-4

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6538-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6538-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6538-73:
(6*6)+(5*5)+(4*3)+(3*8)+(2*7)+(1*3)=114
114 % 10 = 4
So 6538-73-4 is a valid CAS Registry Number.

6538-73-4SDS

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 N-[2-(3-prop-1-en-2-ylphenyl)propan-2-yl]-2-(1,3,3-trimethylindol-2-ylidene)acetamide

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

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More Details:6538-73-4 SDS

6538-73-4Downstream Products

6538-73-4Relevant academic research and scientific papers

Enzymes in organic synthesis. 33. Stereoselective pig liver esterase-catalyzed hydrolyses of meso cyclopentyl-, tetrahydrofuranyl-, and tetrahydrothiophenyl-1,3-diesters

Jones, J. Bryan,Hinks, R. Scott,Hultin, Philip G.

, p. 452 - 456 (2007/10/02)

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective.While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters.The enantiomeric excess levels induced are in the 34-46percent range.

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