87656-31-3 Usage
Uses
Used in Perfumery Industry:
2-(diMethoxyMethyl)Methyl benzoate is used as a perfume fixative for its ability to extend the longevity of fragrances, helping to maintain the scent over time.
Used in Pest Control:
2-(diMethoxyMethyl)Methyl benzoate is used as an insecticide for its effectiveness in treating scabies and lice, serving as a topical antiparasitic agent.
Used in Pharmaceutical Industry:
2-(diMethoxyMethyl)Methyl benzoate is used in the manufacturing of pharmaceutical products, capitalizing on its insecticidal properties for medicinal purposes.
Used in Soap Manufacturing:
2-(diMethoxyMethyl)Methyl benzoate is used in the production of soap, where its pleasant odor and fixative properties enhance the sensory experience and effectiveness of the product.
Used in Flavoring Industry:
2-(diMethoxyMethyl)Methyl benzoate is used as a flavoring agent, leveraging its sweet, balsamic scent to improve the taste and aroma of various food products.
It is crucial to handle 2-(diMethoxyMethyl)Methyl benzoate with care, as it has the potential to cause irritation or allergic reactions in some individuals, necessitating proper precautions during its use in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 87656-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,5 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87656-31:
(7*8)+(6*7)+(5*6)+(4*5)+(3*6)+(2*3)+(1*1)=173
173 % 10 = 3
So 87656-31-3 is a valid CAS Registry Number.
87656-31-3Relevant academic research and scientific papers
Synthesis of isocoumarins via palladium catalyzed reactions of methyl 2- (2',2'-dibromovinyl)benzoates
Wang, Le,Shen, Wang
, p. 7625 - 7628 (2007/10/03)
3-Substituted isocoumarins are synthesized in good to excellent yields via palladium catalyzed coupling of 2-(2',2'-dibromovinyl)benzoates and organostannanes. The process involves a Stille reaction, and a subsequent annulation reaction.