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Phenol, 4-(1-phenylcyclohexyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41768-83-6

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41768-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41768-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,6 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41768-83:
(7*4)+(6*1)+(5*7)+(4*6)+(3*8)+(2*8)+(1*3)=136
136 % 10 = 6
So 41768-83-6 is a valid CAS Registry Number.

41768-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(1-phenylcyclohexyl)phenol

1.2 Other means of identification

Product number -
Other names F0020-1561

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:41768-83-6 SDS

41768-83-6Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS FOR TREATING NEURODEGENERATIVE DISEASES

-

Page/Page column 47, (2014/09/03)

The present application relates to a composition comprising a selective androgen modulating compound of formula (I) and selective estrogen receptor β agonist of formula (II). The present application also relates to the use of a selective androgen modulating compound of formula (I) in combination with a selective estrogen receptor β agonist of formula (II) in the treatment or prevention of neurodegenerative diseases or disorders,such as Alzheimer's disease, Huntigton's disease, Parkinson's disease, depression, anxiety, multiple sclerosis, symptoms associated with or caused by multiple sclerosis, and acute or chronic pain.

SUBSTITUTED DIHYDRO AND TETRAHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

-

Page/Page column 24, (2010/04/23)

The present invention relates to a series of substituted dihydro and tetrahydro oxazolopyrimidinones, specifically, to a series of 2-substituted-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-ones and 2-substituted-2,3,5,6-tetra-hydro-oxazolo[3,2-a]pyrimidin-7-ones of formula (I): Wherein p, n, X, Y, R1, R2, R3, R4, R5, R6, R7 and R8 are as defined herein. This invention also relates to methods of making these compounds including novel intermediates. The compounds of this invention are modulators of metabotropic glutamate receptors (mGluR), particularly, mGluR2 receptor. Therefore, the compounds of this invention are useful as pharmaceutical agents, especially in the treatment and/or prevention of a variety of central nervous system disorders (CNS), including but not limited to acute and chronic neurodegenerative conditions, psychoses, convulsions, anxiety, depression, migraine, pain, sleep disorders and emesis.

COMPOUNDS WITH ACTIVITY AT ESTROGEN RECEPTORS

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Page/Page column 58, (2010/11/30)

Disclosed herein are methods of treating neuropathic pain, reducing inflammation, reducing IL-4 levels, and reducing IFN-γ levels, using various di-aromatic compounds for use as estrogen receptors β agonists.

COMPOUNDS WITH ACTIVITY AT ESTROGEN RECEPTORS

-

Page/Page column 47, (2010/02/14)

Disclosed herein are novel di-phenyl compounds and methods for using various di-phenyl compounds for treatment and prevention of diseases and disorders related to estrogen receptors.

REACTION OF PHENOL WITH 1-PHENYL-1-CYCLOHEXENE IN THE PRESENCE OF ALUMINUM PHENOLATE

Kozlikovskii, Ya. B.,Koshchii, V. A.

, p. 844 - 846 (2007/10/02)

The reaction of phenol with 1-phenyl-1-cyclohexene in the presence of aluminum phenolate leads to 1-phenyl-1-(p-hydroxyphenyl)-, 1-phenyl-2-(p-hydroxyphenyl)-, 1-phenyl-2-(o-hydroxyphenyl)-, and 1-phenyl-3-(o-hydroxyphenyl)cyclohexanes, in which the ortho-alkylation products predominate.The products from ionic hydrogenation and dehydrogenation of the initial olefin (phenylcyclohexane and biphenyl) and a small amount of the products from the cleavage of the phenyl(hydroxyphenyl)cyclohexanes are also formed.

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