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3,5-Dimethylcyclohex-1-ene-4-carboxaldehyde is an organic compound with the molecular formula C9H14O. It is a colorless to pale yellow liquid with a strong, sweet, and fruity odor. This aldehyde is commonly used as a fragrance ingredient in various applications, such as perfumes, cosmetics, and household products. It is also known as "Lyral" and is characterized by its floral scent, reminiscent of muguet (lily of the valley). The compound is synthesized through a series of chemical reactions, including the condensation of acetone with propionaldehyde and subsequent cyclization. Due to its pleasant aroma, 3,5-Dimethylcyclohex-1-ene-4-carboxaldehyde is a popular choice in the fragrance industry, contributing to the creation of many well-known perfumes and scented products.

6975-94-6

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6975-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6975-94-6 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 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6975-94:
(6*6)+(5*9)+(4*7)+(3*5)+(2*9)+(1*4)=146
146 % 10 = 6
So 6975-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H14O/c1-7-4-3-5-8(2)9(7)6-10/h3-4,6-9H,5H2,1-2H3

6975-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylcyclohex-3-ene-1-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,6-Dimethyl-cyclohex-3-encarbaldehyd

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 -
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More Details:6975-94-6 SDS

6975-94-6Relevant academic research and scientific papers

Selective Production of Renewable para-Xylene by Tungsten Carbide Catalyzed Atom-Economic Cascade Reactions

Dai, Tao,Li, Changzhi,Li, Lin,Zhao, Zongbao Kent,Zhang, Bo,Cong, Yu,Wang, Aiqin

supporting information, p. 1808 - 1812 (2018/02/10)

Tungsten carbide was employed as the catalyst in an atom-economic and renewable synthesis of para-xylene with excellent selectivity and yield from 4-methyl-3-cyclohexene-1-carbonylaldehyde (4-MCHCA). This intermediate is the product of the Diels–Alder reaction between the two readily available bio-based building blocks acrolein and isoprene. Our results suggest that 4-MCHCA undergoes a novel dehydroaromatization–hydrodeoxygenation cascade process by intramolecular hydrogen transfer that does not involve an external hydrogen source, and that the hydrodeoxygenation occurs through the direct dissociation of the C=O bond on the W2C surface. Notably, this process is readily applicable to the synthesis of various (multi)methylated arenes from bio-based building blocks, thus potentially providing a petroleum-independent solution to valuable aromatic compounds.

CHEMISTRY OF ENOL ETHERS. LIII. PROTOTROPIC ISOMERIZATION IN THE SERIES OF CYCLIC 1-ALKOXY-1,4-DIENES

Makin, S. M.,Pomogaev, A. I.,Boiko, T. N.,Nikiforova, A. P.

, p. 2033 - 2036 (2007/10/02)

A series of diethyl acetals of 1-cyclohexene-3-carbaldehydes, the pyrolysis of which leads to the formation of cyclic 1-ethoxy-1,4-dienes, were obtained by the acetalization of 1-cyclohexene-3-carbaldehydes, which were obtained by the condensation of conjugated dienes with α,β-unsaturated aldehydes.The prototropic isomerization of the 1-ethoxy-1,4-dienes to corresponding 1-ethoxy-1,3-dienes under the influence of potassium tert-butoxide in dimethyl sulfoxide solution was investigated.

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