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2,2,3,6-tetramethylcyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59860-58-1

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59860-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59860-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,6 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59860-58:
(7*5)+(6*9)+(5*8)+(4*6)+(3*0)+(2*5)+(1*8)=171
171 % 10 = 1
So 59860-58-1 is a valid CAS Registry Number.

59860-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,6-Tetramethylcyclohexanone

1.2 Other means of identification

Product number -
Other names 2,5,6,6-Tetramethyl-cyclohexanon

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:59860-58-1 SDS

59860-58-1Relevant academic research and scientific papers

Aliphatic alcohols, their preparation and use of same as perfuming ingredients

-

, (2008/06/13)

Novel cycloaliphatic alcohols of formula STR1 wherein each of symbols R1 and R2 designates a methyl radical or wherein R1 designates an ethyl radical and R2 stands for a methyl radical or a hydrogen atom, posses

208. Diastereoselektivitaet der Geruchswahrnehmung von Alkoholen der Iononreihe

Schulte-Elte, Karl H.,Giersch, Wolfgang,Winter, Beat,Pamingle, Herve,Ohloff, Guenther

, p. 1961 - 1985 (2007/10/02)

The characteristic odor of the diastereoisomers 1 and 2 of 1-(2,2,6-trimethylcyclohexyl)-3-hexanol is configuration dependent, the trans-alcohol 1 being identified as the sensorily active component.Structure modifications of model 1/2, for example substitution on C(2), C(13), and C(14) (ionon numbering) by CH3 groups, introduction of double bonds in the 3- or 4-position, and isosteric substitution of C(7) by an O-atom, leads to analogues revealing an unequivocal relation between stereochemistry and odor.The specific odor of alcohol 1 is generally released when all substituents are in an equatorial position; the resulting analogy with the molecular size and shape of odoriferous steroids suggests that the release of the particular scent can be correlated with a steroid-resembling receptor event.

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