113150-67-7 Usage
Description
BENZYL-VINYL CARBONATE is an organic compound that is utilized as a reagent in the synthesis of various carbonates and is also employed in the production of immunosuppressive compounds. It is a versatile molecule with potential applications in different industries due to its unique chemical properties.
Uses
Used in Pharmaceutical Industry:
BENZYL-VINYL CARBONATE is used as a reagent for the synthesis of immunosuppressive compounds, which are essential in the development of medications that help prevent the body's immune system from attacking transplanted organs or treating autoimmune diseases. Its role in this application is to facilitate the creation of these vital compounds, contributing to advancements in medical treatments.
Used in Chemical Synthesis:
In the chemical industry, BENZYL-VINYL CARBONATE is used as a reagent for the synthesis of varying carbonates. These carbonates have a wide range of applications, from being used as solvents, propellants, and fuels to their utilization in the production of polymers and pharmaceuticals. BENZYL-VINYL CARBONATE plays a crucial role in the creation of these diverse carbonates, showcasing its importance in the chemical synthesis process.
Check Digit Verification of cas no
The CAS Registry Mumber 113150-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,5 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113150-67:
(8*1)+(7*1)+(6*3)+(5*1)+(4*5)+(3*0)+(2*6)+(1*7)=77
77 % 10 = 7
So 113150-67-7 is a valid CAS Registry Number.
113150-67-7Relevant articles and documents
Vinyl carbonates as novel alkoxycarbonylation reagents in enzymatic synthesis of carbonates
Pozo,Pulido,Gotor
, p. 6477 - 6484 (2007/10/02)
Carbonates could be obtained by enzymatic alkoxycarbonylation from vinyl carbonates, which are easily prepared from vinyl chloroformate. The reaction was catalyzed by Candida antarctica lipases, SP 435 and SP 435 A. The method could be also used for the synthesis of carbamates. When racemic alcohols were used, lipase catalyzed their resolution, and chiral carbonates were obtained with different enantiomeric excesses depending upon the structure of the alcohol.
