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4-methyl-2-(6-methylcyclohex-3-en-1-yl)-1,3-dioxolane is a complex organic compound with the molecular formula C11H18O2. It features a 1,3-dioxolane ring, which is a five-membered cyclic ether with two oxygen atoms and three carbon atoms. The compound has a methyl group attached to the 4-position of the dioxolane ring and a 6-methylcyclohex-3-en-1-yl group at the 2-position. The 6-methylcyclohex-3-en-1-yl group consists of a cyclohexene ring with a methyl group at the 6-position and a double bond between the 3 and 4 carbons. This chemical structure contributes to its unique properties and potential applications in various fields, such as pharmaceuticals or chemical research.

6976-73-4

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6976-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6976-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6976-73:
(6*6)+(5*9)+(4*7)+(3*6)+(2*7)+(1*3)=144
144 % 10 = 4
So 6976-73-4 is a valid CAS Registry Number.

6976-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-(6-methylcyclohex-3-en-1-yl)-1,3-dioxolane

1.2 Other means of identification

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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

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More Details:6976-73-4 SDS

6976-73-4Downstream Products

6976-73-4Relevant academic research and scientific papers

Chemistry of dioxacycloalkanes: VII. Synthesis and properties of substituted 1,3-dioxolanes derived from carbocyclic aldehydes

Kerimov

, p. 136 - 140 (2001)

Reactions of 3-cyclohexenecarbaldehyde, 6-methyl-3-cyclohexenecarbaldehyde, bicyclo[2.2.1]-hept-5-ene-endo-2-carbaldehyde, and benzaldehyde with 1,2-propanediol and 3-chloro-1,2-propanediol gave the corresponding 2,4-substituted 1,3-dioxolanes. Their reactions with peroxyacetic acid, bromine, dichlorocarbene, and nucleophiles were studied. The effect of the substituents in the diol and aldehyde on their relative reactivity is discussed.

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