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78842-55-4

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78842-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78842-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,4 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78842-55:
(7*7)+(6*8)+(5*8)+(4*4)+(3*2)+(2*5)+(1*5)=174
174 % 10 = 4
So 78842-55-4 is a valid CAS Registry Number.

78842-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6,6-trimethylcyclohexen-1-yl)-1,3-dioxolane

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:78842-55-4 SDS

78842-55-4Relevant articles and documents

Ring A building blocks for taxoids and taxamycins

Tjepkema, Michael W.,Wilson, Peter D.,Audrain, Helene,Fallis, Alex G.

, p. 1215 - 1224 (2007/10/03)

The synthesis of a series of oxygenated cyclohexene ring A synthons 20, 22-27, 34, 36, and 37 that possess suitable functionality for further elaboration for taxoid synthesis are described. These compounds have been prepared from β-ionone by a series of oxidative and addition reactions or alternatively by Lewis acid catalyzed Diels-Alder cycloadditions with the oxygen-containing trimethyl substituted dienes 31 and 33. The syntheses of a series of oxygenated cyclohexene ring A synthons 20, 22-27, 34, 36, and 37 that possess suitable functionality for further elaboration for taxoid synthesis are described. These compounds have been prepared from β-ionone by a series of oxidative and addition reactions or alternatively by Lewis acid catalyzed Diels-Alder cycloadditions with the oxygen-containing trimethyl substituted dienes 31 and 33.

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