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91008-94-5

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91008-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91008-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,0 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91008-94:
(7*9)+(6*1)+(5*0)+(4*0)+(3*8)+(2*9)+(1*4)=115
115 % 10 = 5
So 91008-94-5 is a valid CAS Registry Number.

91008-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Octane, 4,4-dimethoxy-

1.2 Other means of identification

Product number -
Other names 4,4-Dimethoxyoctane

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:91008-94-5 SDS

91008-94-5Downstream Products

91008-94-5Relevant articles and documents

Revisiting the Influence of Silver in Cationic Gold Catalysis: A Practical Guide

Lu, Zhichao,Han, Junbin,Hammond, Gerald B.,Xu, Bo

supporting information, p. 4534 - 4537 (2015/09/28)

An excess amount of silver salt to generate cationic gold from a gold catalyst precursor such as L-Au-Cl almost always has adverse effects on the reactivity of the cationic gold catalyst. A preformed L-Au+X- complex, generated by sonication followed by centrifugation, increases the reactivity in a gold catalyzed reaction. The adverse silver effect might be caused by the interaction of silver salts with gold intermediates.

THE BEHAVIOUR OF DISUBSTITUTED ALKYNES WITH VARIOUS METAL ION ACETATES

Bassetti, Mauro,Floris, Barbara

, p. 595 - 598 (2007/10/02)

4-Octyne and diphenylethyne have been treated with some metal ion acetates in methanol and in acetic acid.From this systematic investigation, it appeares that the metal ions play a major role in directing the course of the reaction.The function of the metal is not predictable, since no general trend has been observed.Mercuric acetate was by and large the best reagent for the reaction with alkynes, quantitatively transforming these substrates into vinyl ethers, ketones, and dimethylketals.The reaction was faster in methanol than in acetic acid, and 4-octyne resulted more reactive than diphenylethyne.

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