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490-20-0 Usage

General Description

2β,4α-Diphenyl-1β,3α-cyclobutanedicarboxylic acid is a chemical compound with a complex molecular structure. It contains two phenyl groups attached to carbon atoms at positions 2 and 4, and a cyclobutane ring with carboxylic acid groups at positions 1 and 3. 2β,4α-Diphenyl-1β,3α-cyclobutanedicarboxylic acid is a derivative of cyclobutane and is commonly used in the synthesis of various organic molecules through its reactivity as a diacid. It has potential applications in pharmaceutical and material science research due to its unique structure and properties. The compound's molecular structure and properties make it a subject of interest for further study and potential applications in various fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 490-20-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 490-20:
(5*4)+(4*9)+(3*0)+(2*2)+(1*0)=60
60 % 10 = 0
So 490-20-0 is a valid CAS Registry Number.

490-20-0SDS

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 2,4-diphenylcyclobutane-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2c,4t-Diphenyl-cyclobutan-1r,3t-dicarbonsaeure

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:490-20-0 SDS

490-20-0Relevant articles and documents

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Bernstein,Quimby

, p. 1845 (1943)

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Transient states in [2 + 2] photodimerization of cinnamic acid: Correlation of solid-state NMR and X-ray analysis

Khan, Mujeeb,Brunklaus, Gunther,Enkelmann, Volker,Spiess, Hans-Wolfgang

, p. 1741 - 1748 (2008)

13C-CPMAS and other solid-state NMR methods have been applied to monitor the solid-state reactions of trans-cinnamic acid derivatives, which are the pioneer and model compounds in the field of topochemistry previously studied by X-ray diffracti

SAR studies on truxillic acid mono esters as a new class of antinociceptive agents targeting fatty acid binding proteins

Yan, Su,Elmes, Matthew W.,Tong, Simon,Hu, Kongzhen,Awwa, Monaf,Teng, Gary Y.H.,Jing, Yunrong,Freitag, Matthew,Gan, Qianwen,Clement, Timothy,Wei, Longfei,Sweeney, Joseph M.,Joseph, Olivia M.,Che, Joyce,Carbonetti, Gregory S.,Wang, Liqun,Bogdan, Diane M.,Falcone, Jerome,Smietalo, Norbert,Zhou, Yuchen,Ralph, Brian,Hsu, Hao-Chi,Li, Huilin,Rizzo, Robert C.,Deutsch, Dale G.,Kaczocha, Martin,Ojima, Iwao

, p. 233 - 252 (2018/05/28)

Fatty acid binding proteins (FABPs) serve as critical modulators of endocannabinoid signaling by facilitating the intracellular transport of anandamide and whose inhibition potentiates anandamide signaling. Our previous work has identified a novel small-m

The Antinociceptive Agent SBFI-26 Binds to Anandamide Transporters FABP5 and FABP7 at Two Different Sites

Hsu, Hao-Chi,Tong, Simon,Zhou, Yuchen,Elmes, Matthew W.,Yan, Su,Kaczocha, Martin,Deutsch, Dale G.,Rizzo, Robert C.,Ojima, Iwao,Li, Huilin

, p. 3454 - 3462 (2017/07/17)

Human FABP5 and FABP7 are intracellular endocannabinoid transporters. SBFI-26 is an α-truxillic acid 1-naphthyl monoester that competitively inhibits the activities of FABP5 and FABP7 and produces antinociceptive and anti-inflammatory effects in mice. The

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