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138842-95-2

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138842-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138842-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138842-95:
(8*1)+(7*3)+(6*8)+(5*8)+(4*4)+(3*2)+(2*9)+(1*5)=162
162 % 10 = 2
So 138842-95-2 is a valid CAS Registry Number.

138842-95-2SDS

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 trans-tetrahydropyran-2-yl retinyl ether

1.2 Other means of identification

Product number -
Other names 3,7-Dimethyl-9-tetrahydropyran-2-yloxy-1-(2,6,6-trimethyl-cyclohex-1-enyl)-nona-1,3,5,7-tetraen

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:138842-95-2 SDS

138842-95-2Downstream Products

138842-95-2Relevant articles and documents

Cross-coupling reactions of organosilicon compounds in the stereocontrolled synthesis of retinoids

Bergueiro, Julian,Montenegro, Javier,Cambeiro, Fermin,Saa, Carlos,Lopez, Susana

supporting information; experimental part, p. 4401 - 4410 (2012/06/01)

This paper presents a full account of the use of Hiyama cross-coupling reactions in a highly convergent approach to retinoids in which the key step is construction of the central C10-C11 bond. Representatives of two families of oxygen-activated dienyl silanes (ethoxysilanes and silanols) and of all reported families of "safety-catch" silanols (siletanes, silyl hydrides, allyl-, benzyl-, aryl-, 2-pyridyl- and 2-thienylsilanes) were regio- and stereoselectively prepared and stereospecifically coupled to an appropriate electrophile by treatment with a palladium catalyst and a nucleophilic activator. Both all-trans and 11-cis-retinoids, and their chain-demethylated analogues, were obtained in good yields regardless of the geometry (E/Z) and of the steric congestion in each fragment. This comprehensive study conclusively establishes the Hiyama cross-coupling reaction, with its mild reaction conditions and stable, easily prepared, ecologically advantageous silicon-based coupling partners, as the most effective route to retinoids reported to date.

Hiyama cross-coupling reaction in the stereospecific synthesis of retinoids

Montenegro, Javier,Bergueiro, Julian,Saa, Carlos,Lopez, Susana

body text, p. 141 - 144 (2009/07/04)

The first application of the Hiyama reaction to the synthesis of retinoids is reported. A range of organosilicon moieties (siloxanes, silanols and three kinds of "safety-catch" silanols) were successfully coupled, under activation, to obtain trans-retinol or 11-cis-retinol with high yield and stereoselectivity. The advantageous properties of the silicon-based coupling partners and the mild reaction conditions firmly establish the Hiyama reaction as a viable (even superior) alternative to the traditional Suzuki and Stille couplings in the retinoid field.

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