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5-methyl-2-(propan-2-yl)phenyl naphthalen-1-ylcarbamate is a complex organic compound with the molecular formula C21H21NO2. It is characterized by a naphthalene ring, which is a fused ring system consisting of two benzene rings, and a carbamate functional group. The molecule also features a methyl group at the 5th position and a propyl group attached to the 2nd position of the phenyl ring. This chemical structure contributes to its unique properties and potential applications, which may include use as an intermediate in the synthesis of pharmaceuticals or other organic compounds. The specific reactivity and stability of 5-methyl-2-(propan-2-yl)phenyl naphthalen-1-ylcarbamate would depend on the context in which it is used, and further studies would be required to explore its full potential.

6275-64-5

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6275-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6275-64-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6275-64:
(6*6)+(5*2)+(4*7)+(3*5)+(2*6)+(1*4)=105
105 % 10 = 5
So 6275-64-5 is a valid CAS Registry Number.

6275-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-methyl-2-propan-2-ylphenyl) N-naphthalen-1-ylcarbamate

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

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More Details:6275-64-5 SDS

6275-64-5Downstream Products

6275-64-5Relevant academic research and scientific papers

Synthesis, anticholinesterase activity and molecular modeling study of novel carbamate-substituted thymol/carvacrol derivatives

Kurt, Belma Zengin,Gazioglu, Isil,Dag, Aydan,Salmas, Ramin Ekhteiari,Kay?k, Gülru,Durdagi, Serdar,Sonmez, Fatih

, p. 1352 - 1363 (2017/02/18)

New thymol and carvacrol derivatives with the carbamate moiety were synthesized and their inhibitory effects on acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) were evaluated. 5-isopropyl-2-methylphenyl(3-fluorophenyl)carbamate (29) was foun

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