7071-16-1 Usage
Physical state
Colorless liquid At room temperature, the compound exists as a colorless liquid.
Usage in fragrances
Used in cosmetics and personal care products 2-(2-Methylcyclohexylidene)acetaldehyde is used as a fragrance ingredient in various cosmetic and personal care items due to its sweet, fruity odor.
Usage in food
Flavoring agent The compound is also used as a flavoring agent in food products to enhance their taste and aroma.
Application in scented products
Adding pleasant scents to perfumes The sweet, fruity odor of the compound makes it suitable for adding a pleasant scent to perfumes and other scented products.
Industrial applications
Synthetic flavors and fragrances production The compound is used in the production of synthetic flavors and fragrances, contributing to the creation of new and diverse scents.
Pharmaceutical use
Manufacturing of pharmaceuticals 2-(2-Methylcyclohexylidene)acetaldehyde is also utilized in the manufacturing process of various pharmaceuticals and other chemical compounds.
Safety concerns
Potentially harmful It is important to handle 2-(2-Methylcyclohexylidene)acetaldehyde with care, as it can be harmful if it comes into contact with the skin or if it is ingested.
Check Digit Verification of cas no
The CAS Registry Mumber 7071-16-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7071-16:
(6*7)+(5*0)+(4*7)+(3*1)+(2*1)+(1*6)=81
81 % 10 = 1
So 7071-16-1 is a valid CAS Registry Number.
7071-16-1Relevant academic research and scientific papers
A Novel and Highly Stereoselective Approach to Aza-Spirocycles. A Short Total Synthesis of 2-epi-(±)-Perhydrohistrionicotoxin and an Unprecedented Decarboxylation of 2-Pyrones
McLaughlin, Michael J.,Hsung, Richard P.,Cole, Kevin P.,Hahn, Juliet M.,Wang, Jiashi
, p. 2017 - 2020 (2007/10/03)
(Matrix Presented) A novel and highly stereoselective synthesis of aza-spirocycles is described. An application of this methodology is illustrated as a short and concise total synthesis of 2-epi-(±)-perhydrohistrionicotoxin with high diastereomeric contro
