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2,4-Pentadien-1-ol, 5-[3,5-bis(1,1-dimethylethyl)phenyl]-3-methyl-, (2Z,4E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

823192-19-4

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823192-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 823192-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,3,1,9 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 823192-19:
(8*8)+(7*2)+(6*3)+(5*1)+(4*9)+(3*2)+(2*1)+(1*9)=154
154 % 10 = 4
So 823192-19-4 is a valid CAS Registry Number.

823192-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2Z,4E)-5-(3,5-Di-tert-butyl-phenyl)-3-methyl-penta-2,4-dien-1-ol

1.2 Other means of identification

Product number -
Other names -

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:823192-19-4 SDS

823192-19-4Upstream product

823192-19-4Relevant academic research and scientific papers

9-cis-Retinoic acid analogues with bulky hydrophobic rings: New RXR-selective agonists

Alvarez, Rosana,Vega, M. Jesús,Kammerer, Sabrina,Rossin, Aurélie,Germain, Pierre,Gronemeyer, Hinrich,De Lera, Angel R.

, p. 6117 - 6122 (2004)

Stille cross-coupling of aryltriflates 10 and dienylstannane 11, oxidation and Horner-Wadsworth-Emmons reaction afforded stereoselectively retinoates 15. Saponification provided the carboxylic acids 8a and 8b, retinoids that incorporate a bulky hydrophobic ring while preserving the 9-cis-geometry of the parent system. In contrast to the pan-RAR/RXR agonistic profile of the lower homologue of 8a, compound 7 (LG100567), retinoids 8 showed selective binding and transactivation of RXR, devoid of significant RAR activation. In PLB985 leukemia cells that require RXR agonists for differentiation compounds 8 induced maturation in the presence of the RAR-selective pan-agonist TTNPB; this effect was blocked by an RXR-selective antagonist.

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