7560-65-8 Usage
Description
4-(Dimethoxymethyl)-1-cyclohexene is a cycloalkene derivative with the molecular formula C9H16O2. It features a cyclohexene ring with two methoxy groups and a methylene bridge attached, providing unique structural and reactive properties that make it a valuable intermediate in organic synthesis.
Uses
Used in Organic Synthesis:
4-(Dimethoxymethyl)-1-cyclohexene is utilized as a building block for the production of various pharmaceuticals and fine chemicals. Its unique structure and reactivity contribute to the synthesis of complex organic molecules, making it a valuable component in the creation of a wide range of compounds.
Used in Pharmaceutical Production:
As a key intermediate, 4-(Dimethoxymethyl)-1-cyclohexene is used in the synthesis of various pharmaceuticals, playing a crucial role in the development of new drugs and improving the efficacy of existing ones.
Used in the Preparation of Heteroaromatic Compounds:
4-(Dimethoxymethyl)-1-cyclohexene also serves as a reagent in the preparation of heteroaromatic compounds, which are important in the fields of material science and medicinal chemistry for their diverse applications and properties.
Used in Research and Development:
Chemists leverage 4-(Dimethoxymethyl)-1-cyclohexene as a valuable tool in the development of new materials and drug candidates, taking advantage of its unique characteristics to explore novel chemical reactions and syntheses.
Check Digit Verification of cas no
The CAS Registry Mumber 7560-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7560-65:
(6*7)+(5*5)+(4*6)+(3*0)+(2*6)+(1*5)=108
108 % 10 = 8
So 7560-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-10-9(11-2)8-6-4-3-5-7-8/h3-4,8-9H,5-7H2,1-2H3
7560-65-8Relevant articles and documents
A (3 - alkoxy - 4 - hydroxy) - cyclohexyl acetal glycol and its isomers of use
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Paragraph 0054-0055, (2017/08/26)
The present invention discloses a (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol, an (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol and synthesis methods and use therefor. The (3-alkoxy-4-hydroxy)-cyclohexyl methylal diol and (3-hydroxy-4-alkoxy)-cyclohexyl methylal diol can be used for synthesis of a variety of vanillin and iso-vanillin. Compared to the existing synthetic method, the synthesis method has simple steps, and less discharge of "three wastes".
Efficient acetalisation of aldehydes catalyzed by titanium tetrachloride in a basic medium
Clerici, Angelo,Pastori, Nadia,Porta, Ombretta
, p. 15679 - 15690 (2007/10/03)
The acetalisation of aliphatic and aromatic aldehydes is achieved in a basic medium by using catalytic amount of Ti(IV) chloride in MeOH in the presence of NH3 or Et3N. The present protocol shows many advantages over the well known base or acid catalysis: in fact, in contrast to base-promoted acetalisation, aldehydes with electron-rich carbonyl groups react easily, enolizable aldehydes do not undergo aldol condensation and, in contrast to acid-catalysis, migration of the double bond does not occur in the preparation of α,β-unsaturated acetals.
