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4-Acetyl-4-methylcyclohexanone is a chemical compound with the molecular formula C9H14O2. It is a ketone, meaning it contains a carbonyl group (C=O) bonded to two carbon atoms. 4-Acetyl-4-methylcyclohexanone has a pleasant, fruity odor and is considered to be relatively stable under normal conditions.

6848-93-7

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6848-93-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Acetyl-4-methylcyclohexanone is used as an intermediate in the production of drugs. It serves as a reagent in organic synthesis, enabling the creation of various pharmaceutical compounds through different chemical reactions.
Used in Perfume Industry:
4-Acetyl-4-methylcyclohexanone is used as an intermediate in the production of fragrances. Its pleasant, fruity odor makes it a valuable component in the formulation of perfumes and other scented products.
It is important to handle 4-Acetyl-4-methylcyclohexanone with care and follow proper safety precautions when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 6848-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6848-93:
(6*6)+(5*8)+(4*4)+(3*8)+(2*9)+(1*3)=137
137 % 10 = 7
So 6848-93-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O2/c1-7(10)9(2)5-3-8(11)4-6-9/h3-6H2,1-2H3

6848-93-7SDS

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 4-acetyl-4-methylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,4-acetyl-4-methyl

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:6848-93-7 SDS

6848-93-7Relevant academic research and scientific papers

Synthesis of substituted tricyclo[5.3.1.04,9]undecan-2,6-dione from 4,4-disubstituted cyclohexanone enamines and methacryloyl chloride

Ahmed, M. Giasuddin,Ahmed, Syeda Asghari,Akhter, Kawsari,Tsuda, Yoshisuke,Hossain, M. Mahmun,Forsterling, F. Holger

, p. 1273 - 1283 (2007/10/03)

Morpholine enamines 4-acetyl-4-methyl-1-morpholinocyclohexene 4a, 4-acetyl-4-phenyl-1-morpholinocyclohexene 4b, and 4-acetyl-4-isopropenyl-1- morpholinocyclohexene 4c react with methacryloyl chloride to give 1,7-dimethyl-4(N-morpholino) tricyclo[5.3.1.0s

Transmission of Polar Substituent Effects Through the Bicyclooctane Ring System as Monitored by NMR Shifts: a 13C NMR Study of 4-Substituted-1-methylbicyclooctanes

Adcock, William,Abeywickrema, Anil N.,Iyer, V. Sankar,Kok, Gaik B.

, p. 213 - 220 (2007/10/02)

Carbon-13 substituent chemical shifts (SCS) are reported for the methyl group of a series of 4-substituted 1-methylbicyclooctanes covering a wide range of electronic substituent effects.Unlike the 13C SCS of the α-carbon centre in various unsaturat

The Synthesis of 1,4-Disubstituted Bicyclooctanes exhibiting Wide-range, Enantiotropic Nematic Phases

Gray, George W.,Kelly, Stephen M.

, p. 26 - 31 (2007/10/02)

The 1,4-disubstituted bicyclooctane ring has been incorporated in certain cyano-substituted systems to produce series of mesogens exhibiting wide-range nematic phases. 1-(4-Cyanophenyl)- and 1-(4'-cyanobiphenyl-4-yl)-4-n-alkylbicyclooctanes

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