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1,4-Cyclohexanediol, 1-methyl-4-(1-methylethyl)-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17948-61-7

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17948-61-7 Usage

Chemical structure

Cyclohexane ring with two hydroxyl groups (-OH) at positions 1 and 4, a methyl group (-CH3) at position 1, and a tert-butyl group (-C(CH3)3) at position 4

Configuration

cis(the hydroxyl groups are on the same side of the cyclohexane ring)

Industrial applications

a. Raw material for the synthesis of pharmaceuticals and agrochemicals
b. Solvent in various products
c. Surfactant in various products

Potential properties

a. Antibacterial
b. Antifungal

Medical and healthcare applications

Useful in certain medical and healthcare applications due to its potential antibacterial and antifungal properties

Physical and chemical properties

The cisconfiguration of the molecule affects its physical and chemical properties, making it suitable for specific applications in industry and research.

Check Digit Verification of cas no

The CAS Registry Mumber 17948-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,4 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17948-61:
(7*1)+(6*7)+(5*9)+(4*4)+(3*8)+(2*6)+(1*1)=147
147 % 10 = 7
So 17948-61-7 is a valid CAS Registry Number.

17948-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-1,4-dihydroxy-1-isopropyl-4-methylcyclohexane

1.2 Other means of identification

Product number -
Other names cis-1-isopropyl-4-methylcyclohexane-1,4-diol

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:17948-61-7 SDS

17948-61-7Relevant academic research and scientific papers

Kinetics of dissociative electron transfer to ascaridole and dihydroascaridole - Model bicyclic endoperoxides of biological relevance

Donkers, Robert L.,Workentin, Mark S.

, p. 4012 - 4020 (2007/10/03)

The homogeneous and heterogeneous electron transfer (ET) reduction of ascaridole (ASC) and dihydroascaridole (DASC), two bicyclic endoperoxides, chosen as convenient models of the bridged bicyclic endoperoxides found in biologically relevant systems, were studied in aprotic media by using electrochemical methods. ET is shown to follow a concerted dissociative mechanism that leads to the distonic radical anion, which is itself reduced in a second step by an overall two-electron process. The kinetics of homogeneous ET to these endoperoxides from an extensive series of radical anion electron donors were measured as a function of the driving force of electron transfer (ΔG°ET). The kinetics of heterogeneous ET were also studied by convolution analysis. Together, the heterogeneous and homogeneous ET kinetic data provide the best example of the parabolic nature of the activation-driving force relationship for a concerted dissociative ET described by Saveant; the data is particularly illustrative due to the low bond-dissociation enthalpy (BDE) of the O-O bond and hence small intrinsic barriers. Analysis of the data allowed the dissociative reduction potentials (E°diss) to be determined as -1.2 and -1.1 Vagainst SCE for ASC and DASC, respectively. Unusually low pre-exponential factors measured in temperature-dependent kinetic studies suggest that ET to these O-O bonded systems is nonadiabatic. Analysis of ET kinetics for ASC and DASC by the Saveant model with a modification for nonadiabaticity allowed the intrinsic free energy for ET to be determined. The use of this approach and estimates for the BDE provide approximations of the reorganization energies. We suggest the methodology described herein can be used to evaluate the extent of ET to other endoperoxides of biological relevance and to provide thermochemical data not otherwise available.

The Diepoxides of Terpinolene

Carman, Raymond M.,Rayner, Anthony C.

, p. 195 - 202 (2007/10/02)

The structures of the racemic 1,2:4,8-diepoxy-p-menthanes, the diepoxides of terpinolene, are revised.The major isomer has the trans relationship between the two epoxides.

Ruthenium(II)-Catalyzed Reactions of 1,4-Epiperoxides

Suzuki, Masaaki,Ohtake, Hiroaki,Kameya, Yoshimi,Hamanaka, Nobuyuki,Noyori, Ryoji

, p. 5292 - 5302 (2007/10/02)

The behavior of 1,4-epiperoxides in the presence of transition-metal complexes is highly dependent on the structures of the substrates and the nature of the metal catalysts.Reaction of saturated epiperoxides such as 1,3-epiperoxycyclopentane, 1,4-epiperoxycyclohexane, or dihydroascaridole catalyzed by RuCl2(PPh3)3 in dichloromethane gives a mixture of products arising from fragmentation, rearrangement, reduction, disproportionation, etc.Prostaglandin H2 methyl ester undergoes clean and stereospecific fragmentation to afford methyl(5Z,8E,10E,12S)-12-hydroxy-5,8,10-heptadecatrienoate and malonaldehyde.Bicyclic 2,3-didehydro 1,4-epiperoxides give the syn-1,2:3,4-diepoxides by the same catalyst.The monocyclic analogues are transformed to a mixture of diepoxides and furan products.The stereochemical outcome of the epoxide formation reflects unique differences in the ground-state geometry of the starting epiperoxide substrates.FeCl2(PPh3)2 serves as a useful catalyst for the skeletal change of sterically hindered bicyclic 2,3-didehydro 1,4-epiperoxides to the syn-diepoxides.In addition, the Fe complex best effects the conversion of 1,4-unsubstituted 2,3-didehydro epiperoxides to furans.The Ru-catalyzed reactions are interpreted in terms of the intermediacy of inner-sphere radicals formed by atom transfer of the Ru(II) species to peroxy substrates, in contrast to the Fe-catalyzed reactions proceeding via free, outer-sphere radicals generated by an electron-transfer mechanism.

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