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7335-11-7

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7335-11-7 Usage

General Description

Cis-4-Cyclohexylcyclohexanol is a chemical compound that belongs to the class of organic compounds known as cyclohexanols. These are compounds containing an alcohol group attached to a cyclohexane ring. Specific to this chemical, two cyclohexane rings are attached to each other in its structure. The 'cis' in its name implies that these two rings are on the same side, giving it a specific geometric shape. Cis-4-Cyclohexylcyclohexanol is not commonly used in the commercial or industrial production of goods or materials as it doesn't have any major or common applications. However, it is often used for scientific research, particularly in the field of chemistry where its structure is used in understanding the behavior of similar compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 7335-11-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7335-11:
(6*7)+(5*3)+(4*3)+(3*5)+(2*1)+(1*1)=87
87 % 10 = 7
So 7335-11-7 is a valid CAS Registry Number.

7335-11-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (1s,4s)-[1,1'-Bi(cyclohexan)]-4-ol

1.2 Other means of identification

Product number -
Other names cis-Bicyclohexyl-4-ol

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:7335-11-7 SDS

7335-11-7Relevant articles and documents

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Smith,W.N.

, p. 4463 - 4465 (1973)

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Hydrogenation of 4-Substituted Biphenyls

Minabe, Masahiro,Watanabe, Kousuke,Ayabe, Yooichi,Yoshida, Masaaki,Toda, Takashi

, p. 1745 - 1748 (2007/10/02)

Hydrogenations of 4-hydroxy-(1a), 4-methoxy-, and 4-methylbiphenyls were carried out in the presence of Raney nickel (R-Ni), palladium-on-carbon (Pd-C), or platinum as catalysts under relatively mild conditions.The reaction rates depend primarily on the catalysts and less on the substrates.Hydrogenation with Pd-C or Pt took place predominantly in the phenyl ring, independent of the substituent.On the other hand, hydrogenation with R-Ni caused reduction mainly in the substituted aromatic ring.Hydrogenation of the phenol, 1a, using R-Ni afforded predominantly trans-4-phenylcyclohexanol in preference to the cis isomer, differing from the other reactions examined.

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