91095-84-0 Usage
Uses
Used in Pharmaceutical Industry:
Pentanoic acid, 3-hydroxy-2-methylene-, 1,1-dimethylethyl ester, (S)is used as a chiral building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of enantiomerically pure compounds, which are essential in the development of effective and safe medications.
Used in Agrochemical Industry:
Pentanoic acid, 3-hydroxy-2-methylene-, 1,1-dimethylethyl ester, (S)is used as a chiral building block in the synthesis of agrochemicals. Its ability to create enantiomerically pure compounds makes it valuable in the development of effective and environmentally friendly pesticides and other agricultural products.
Used as a Flavoring Agent:
Pentanoic acid, 3-hydroxy-2-methylene-, 1,1-dimethylethyl ester, (S)is used as a flavoring agent in the food and beverage industry. Its fruity odor and liquid form make it suitable for adding unique and pleasant flavors to various products.
Used in Organic Chemical Reactions:
Pentanoic acid, 3-hydroxy-2-methylene-, 1,1-dimethylethyl ester, (S)is used in various organic chemical reactions and processes for the production of different compounds. Its versatile structure allows for its use in a wide range of applications, making it a valuable component in the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 91095-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,9 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91095-84:
(7*9)+(6*1)+(5*0)+(4*9)+(3*5)+(2*8)+(1*4)=140
140 % 10 = 0
So 91095-84-0 is a valid CAS Registry Number.
91095-84-0Relevant academic research and scientific papers
SYNTHESIS OF POTENTIALLY ALLERGENIC CHIRAL α-(HYDROXYALKYL)ACRYLATES
Papageorgiou, Christos,Benezra, Claude
, p. 1303 - 1306 (2007/10/02)
The title componds have been synthesized with 75percent enantiomeric excess from chiral p-tolylsulfoxides 1 and aldehydes, followed by thermal elimination of the sulfoxide.
