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110952-26-6

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110952-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110952-26-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,9,5 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110952-26:
(8*1)+(7*1)+(6*0)+(5*9)+(4*5)+(3*2)+(2*2)+(1*6)=96
96 % 10 = 6
So 110952-26-6 is a valid CAS Registry Number.

110952-26-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(5,5,8,8-tetramethyl-6,7-dihydronaphthalene-2-carbonyl)naphthalene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene-2-carbonyl)naphthalene-2-carboxylic acid

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:110952-26-6 SDS

110952-26-6Downstream Products

110952-26-6Relevant articles and documents

Development and Characterization of Novel and Selective Inhibitors of Cytochrome P450 CYP26A1, the Human Liver Retinoic Acid Hydroxylase

Diaz, Philippe,Huang, Weize,Keyari, Charles M.,Buttrick, Brian,Price, Lauren,Guilloteau, Nicolas,Tripathy, Sasmita,Sperandio, Vanessa G.,Fronczek, Frank R.,Astruc-Diaz, Fanny,Isoherranen, Nina

, p. 2579 - 2595 (2016/04/10)

Cytochrome P450 CYP26 enzymes are responsible for all-trans-retinoic acid (atRA) clearance. Inhibition of CYP26 enzymes will increase endogenous atRA concentrations and is an attractive therapeutic target. However, the selectivity and potency of the exist

Bicyclic naphthalenic derivatives, a process for preparing the same and human or veterinary medicines and cosmetic compositions containing said derivatives

-

, (2008/06/13)

A bicyclic naphthalenic compound has the formula STR1 wherein A represents methylene or dimethylene, substituted or not by lower alkyl, R1, R2, R3 and R4 represent hydrogen or lower alkyl, or R1 and R3 taken together form a methylene or dimethylene bridge when A represents dimethylene, R' represents hydrogen, OH, alkoxy having 1-4 carbon atoms, acyloxy having 1-4 carbon atoms or amino, R" represents hydrogen or alkoxy having 1-4 carbon atoms, or r' and R" taken together form an oxo, methano or hydroxyimino group, R represents --CH2 OH or --COR5, R5 represents hydrogen, --OR6 or STR2 R6 represents hydrogen, alkyl having 1-20 carbon atoms, monohydroxyalkyl, polyhydroxyalkyl, aryl or aralkyl optionally substituted, the residue of a sugar or STR3 p is 1, 2 or 3, and r' and r", each independently, represent hydrogen, lower alkyl, monohydroxyalkyl optionally interrupted by a heteroatom, polyhydroxyalkyl, aryl or benzyl optionally substituted, the residue of an amino acid, an aminoester or an aminated sugar, or r' and r" together form with the nitrogen atom to which they are attached, a heterocycle substituted or not, and the salts of said compounds of formula (I) or the optional isomers thereof.

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