99953-33-0 Usage
Description
Methyl 3-bromo-2,2-difluoropropanoate is a colorless liquid chemical compound with the molecular formula C5H7BrF2O2. It has a strong, fruity odor and is commonly used as a building block in organic synthesis.
Uses
Used in Pharmaceutical Industry:
Methyl 3-bromo-2,2-difluoropropanoate is used as a building block for the production of various drugs. Its unique chemical structure allows for the creation of new and innovative pharmaceutical compounds.
Used in Agrochemical Industry:
Methyl 3-bromo-2,2-difluoropropanoate is used in the production of pest control products. Its properties make it a valuable component in the development of effective and targeted agrochemicals.
Used in Specialty Chemicals Manufacturing:
Methyl 3-bromo-2,2-difluoropropanoate is used in the manufacturing of specialty chemicals, where its unique properties can be leveraged to create high-value products.
Used as a Laboratory Reagent:
Methyl 3-bromo-2,2-difluoropropanoate is used as a reagent in laboratory research, where it can be employed in various chemical reactions and experiments to further scientific understanding and discovery.
Safety Considerations:
Methyl 3-bromo-2,2-difluoropropanoate is considered to be a moderately hazardous chemical. Appropriate safety measures should be taken when handling and storing it to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 99953-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,9,5 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 99953-33:
(7*9)+(6*9)+(5*9)+(4*5)+(3*3)+(2*3)+(1*3)=200
200 % 10 = 0
So 99953-33-0 is a valid CAS Registry Number.
99953-33-0Relevant articles and documents
REACTIONS OF HALOGEN FLUORIDES. XIII. NEW POSSIBILITIES FOR OXIDATIVE NUCLEOPHILIC FLUORINATION OF BROMINE-SUBSTITUTED ESTERS BY THE HEXACHLOROMELAMINE-HYDROGEN FLUORIDE SYSTEM
Chuvatkin, N. N.,Panteleeva, I. Yu.,Kurskii, Yu. A.,Boguslavskaya, L. S.
, p. 1450 - 1456 (2007/10/02)
Primary, secondary, and tertiary bromine atoms in bromine-substituted esters, including the bromine atoms of the CBr2 group at the α position to the ester group, are substituted effectively by a bromine atom in the hexachloromelamine-liquid hydrogen fluoride system under normal conditions.New methods were developed for the production of alkyl and fluoroalkyl 2,3-dihalogeno-2-fluoropropionates, which are key compounds in the synthesis of α-fluoroacrylates.
