89-94-1 Usage
Description
6-Methylcyclohex-3-enecarbaldehyde is a chemical compound with the molecular formula C8H12O. It is a colorless liquid characterized by a strong, sweet, and floral odor.
Uses
Used in Fragrance Industry:
6-Methylcyclohex-3-enecarbaldehyde is used as a perfume ingredient for its pleasant aroma, contributing to the creation of various fragrances.
Used in Food Industry:
It serves as a flavoring agent in food products, enhancing their taste and appeal.
Used in Pharmaceutical Industry:
6-Methylcyclohex-3-enecarbaldehyde has potential applications in pharmaceuticals, although specific uses are not detailed in the provided materials.
Used in Agrochemical Industry:
6-methylcyclohex-3-enecarbaldehyde also has potential applications in agrochemicals, but the exact uses are not specified in the provided materials.
Safety Note:
It is important to handle 6-methylcyclohex-3-enecarbaldehyde with caution due to its potential harmful effects if swallowed, inhaled, or comes into contact with skin.
Check Digit Verification of cas no
The CAS Registry Mumber 89-94-1 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89-94:
(4*8)+(3*9)+(2*9)+(1*4)=81
81 % 10 = 1
So 89-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O/c1-7-4-2-3-5-8(7)6-9/h2-3,6-8H,4-5H2,1H3
89-94-1Relevant articles and documents
STUDIES OF COMPOUNDS IN THE MENTHANE SERIES. XIX. SYNTHESIS AND PROPERTIES OF TRANS-o-4-MENTHEN-8-OL AND STEREOISOMERIC o-5-METHEN-8-OLS
Bazyl'chik, V. V.,Fedorov, P. I.,Klyuev, N. A.,Dank, E. Kh.
, p. 1320 - 1327 (2007/10/02)
Trans-o-4-Menthen-8-ol and cis- and trans-o-5-menthen-8-ols have been prepared via the Diels-Alder reactions of 1,3-butadiene with crotonaldehyde in the presence of boron trifluoride etherate, and piperylene with methyl acrylate, respectively.The dehydration reactions of these alcohols have been studied in the presence of acetic anhydride and potassium bisulfate; the latter reagent demonstrates a high reaction selectivity.
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.