53045-70-8 Usage
Uses
Used in Food Industry:
2-ethyl-but-3-en-1-ol serves as a flavoring agent, enhancing the taste and aroma of various food products due to its distinctive fruit-like scent.
Used in Perfume and Fragrance Industry:
2-ethyl-but-3-en-1-ol is utilized in the production of perfumes and fragrances, contributing to the creation of pleasant and long-lasting scents for personal care and household products.
Used in Pharmaceutical Industry:
Leveraging its antimicrobial properties, 2-ethyl-but-3-en-1-ol finds application in the pharmaceutical sector, potentially aiding in the development of treatments and products that combat microbial infections.
Used in Cosmetic Industry:
Similarly, in cosmetics, the antimicrobial nature of 2-ethyl-but-3-en-1-ol makes it a valuable ingredient for the development of skincare and beauty products that require preservation and hygiene.
Safety Considerations:
While 2-ethyl-but-3-en-1-ol is considered relatively safe for use, its flammability and potential to cause skin and eye irritation necessitate careful handling and adherence to safety guidelines during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 53045-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,0,4 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53045-70:
(7*5)+(6*3)+(5*0)+(4*4)+(3*5)+(2*7)+(1*0)=98
98 % 10 = 8
So 53045-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O/c1-3-6(4-2)5-7/h3,6-7H,1,4-5H2,2H3
53045-70-8Relevant articles and documents
Catalytic Regiodivergent Kinetic Resolution of Allylic Epoxides: A New Entry to Allylic and Homoallylic Alcohols with High Optical Purity
Pineschi, Mauro,Del Moro, Federica,Crotti, Paolo,Di Bussolo, Valeria,Macchia, Franco
, p. 2099 - 2105 (2007/10/03)
A novel regiodivergent kinetic resolution of a series of allylic epoxides with alkylzinc reagents is described. Results demonstrate the potential of chiral copper-phosphoramidite catalysts for enantiomer differentiation of allylic epoxides, allowing a chiral catalyst-stereoregulated synthesis of cyclic allylic and homoallylic alcohols with high optical purities.
