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935-46-6

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935-46-6 Usage

Structure

Bicyclic compound with a spiro linkage and a methyl substituent at the 7th position

Industrial applications

Production of fragrances, flavors, and related products

Fragrance

Used in perfumes, soaps, and cosmetics for its pleasant and sweet aroma

Solvent

Utilized in various chemical processes

Chemical intermediate

Used in the synthesis of other organic compounds

Health and environmental impacts

Not well documented, proper precautions should be taken when handling and using this chemical

Check Digit Verification of cas no

The CAS Registry Mumber 935-46-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 935-46:
(5*9)+(4*3)+(3*5)+(2*4)+(1*6)=86
86 % 10 = 6
So 935-46-6 is a valid CAS Registry Number.

935-46-6SDS

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 1,4-Dioxaspiro[4.5]decane, 7-methyl-

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:935-46-6 SDS

935-46-6Relevant articles and documents

99.Transferts d'hydrogenes dans les cations radicaux ethylene-acetals derives de cyclopentanones et cyclohexanones

Audier, H. E.,Tabet, J. C.,Fetizon, M.

, p. 903 - 911 (2007/10/02)

Hydrogen Transfer during Decompositions of Molecular Ions of Acetals Derived from Substituted Cyclopentanones and Cyclohexanones.The isomerisation process of ethylene-acetal radical ions of low internal energy has been reinvestigated in more detail .The ring contraction of cyclohexane derivatives into methylcyclopentanes is quite general for these ions.The relative rates of H transfers to the C free resulting from C-C cleavage α to the acetal group plays the most important part in the mechanism.

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