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2,4-Pentadienal, 3-methyl-5-(2,6,6-trimethyl-1,3-cyclohexadien-1-yl)-, (Z,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25528-88-5

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25528-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25528-88-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,2 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25528-88:
(7*2)+(6*5)+(5*5)+(4*2)+(3*8)+(2*8)+(1*8)=125
125 % 10 = 5
So 25528-88-5 is a valid CAS Registry Number.

25528-88-5SDS

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 (2Z,4E)-3-Methyl-5-(2,6,6-trimethylcyclohexa-1,3-dien-1-yl)penta-2,4-dien-1-al

1.2 Other means of identification

Product number -
Other names (2Z,4E)-3-Methyl-5-(2,6,6-trimethyl-cyclohexa-1,3-dienyl)-penta-2,4-dienal

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:25528-88-5 SDS

25528-88-5Relevant academic research and scientific papers

Syntheses of high specific activity 2,3- and 3,4-[3H]2-9-cis-retinoic acid

Bennani,Boehm

, p. 1195 - 1200 (2007/10/02)

9-cis-Retinoic acid (9-cis-RA) is an endogenous hormone which binds and activates the retinoic acid receptors (RARs) and the retinoic X receptors (RXRs). In order to investigate the function of 9-cis-RA in vitro and in vivo high specific activity labeled 9-cis-RA was prepared. Two tritium labels were efficiently introduced at the 2,3- or 3,4-positions, respectively, in the cyclohexene ring moiety resulting in labeled 9-cis-RA with specific activity of 58-60 Ci/mmol. The critical ring-labeling step relies on a highly regioselective tritiation of either a terminal or an isolated double bond in the presence of the conjugated retinoate side chain. Moreover, the labeling is performed at the penultimate synthetic step resulting in optimization of radiochemical yields and ease of synthesis. This is the first reported synthesis of ring-labeled [3H]2-9-cis-Ra, and the methodology described herein is applicable to the synthesis of other retinoic acid isomers.

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