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2-Cyclohexen-1-one, 6-hydroxy-3-methyl-6-(1-methylethyl)-, also known as 6-hydroxy-3-methyl-6-isopentyl-2-cyclohexen-1-one, is a chemical compound with the molecular formula C11H18O2. It is a cyclic ketone with a hydroxyl group and an isopentyl side chain. 2-Cyclohexen-1-one, 6-hydroxy-3-methyl-6-(1-methylethyl)- is characterized by its unique structure, which includes a cyclohexenone ring with a double bond, a hydroxyl group at the 6-position, and a methyl and isopentyl group at the 3 and 6 positions, respectively. It is an organic compound that may be found in various natural products and can be used in the synthesis of other chemicals. Due to its specific functional groups and structural features, it has potential applications in the fields of pharmaceuticals, fragrances, and other chemical industries.

1197-72-4

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1197-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197-72-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1197-72:
(6*1)+(5*1)+(4*9)+(3*7)+(2*7)+(1*2)=84
84 % 10 = 4
So 1197-72-4 is a valid CAS Registry Number.

1197-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-3-methyl-6-propan-2-ylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 6-hydroxy-6-isopropyl-3-methylcyclohex-2-enone

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:1197-72-4 SDS

1197-72-4Downstream Products

1197-72-4Relevant academic research and scientific papers

THE VOLATILES OF CALAMINTHA NEPETA SUBSP. GLANDULOSA

De Pooter, Herman L.,De Buyck, Laurent F.,Schamp, Niceas M.

, p. 691 - 694 (1986)

The volatiles of C. nepeta subsp. glandulosa were studied by analysis of the essential oil and of the headspace (after concentration on Tenax GS).Amongst the 27 compounds identified in the essential oil, up to 92percent consisted of piperitone oxide and p

HYDROXYLATION OF PIPERITONE BY CELL SUSPENSION CULTURES OF CATHARANTHUS ROSEUS

Hamada, Hiroki,Fuchikami, Yoshihiro,Ikematsu, Yuka,Hirata, Toshifumi,Williams, Howard J.,Scott, A. Ian

, p. 1037 - 1038 (2007/10/02)

Cell suspension cultures of Catharanthus roseus regioselectively hydroxylate the 4- and 6-positions of (-)-(R)-piperitone. - Key words: Catharanthus roseus; biotransformation; hydroxylation; cell suspension cultures; piperitone.

THE ABSOLUTE CONFIGURATION OF THE DICIPIENE DITERPENES

Croft, K. D.,Ghisalberti, E. L.,Jefferies, P. R.,Stuart, A. D.

, p. 383 - 387 (2007/10/02)

The absolute configuration of the dicipiene diterpenes has been determined by degradation to 4R-4-(2-methoxy-4-methylphenyl)-pentanoic acid.Photolysis of 1,18-diacetoxy-13-oxodecipi-14-ene proceeds through a novel photochemical reaction, formally a cycloreversion, to generate a key intermediate for the degradation.

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