71172-41-3 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 2,3-DIBROMOISOBUTYRATE is used as a key intermediate in the synthesis of various pharmaceutical products for its ability to facilitate the creation of complex organic molecules. Its unique chemical structure allows it to be a valuable component in the development of new drugs and medicines.
Used in Organic Synthesis:
ETHYL 2,3-DIBROMOISOBUTYRATE is used as a reagent in organic synthesis for its capacity to react with other compounds to form new organic molecules. This property makes it instrumental in the production of a wide range of organic compounds used in various industries, including the chemical and pharmaceutical sectors.
Used in Research and Development:
In the field of research and development, ETHYL 2,3-DIBROMOISOBUTYRATE is utilized as a building block for the synthesis of novel organic compounds. Its application in this context aids scientists in exploring new chemical reactions and developing innovative materials with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 71172-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,1,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71172-41:
(7*7)+(6*1)+(5*1)+(4*7)+(3*2)+(2*4)+(1*1)=103
103 % 10 = 3
So 71172-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10Br2O2/c1-3-10-5(9)6(2,8)4-7/h3-4H2,1-2H3
71172-41-3Relevant articles and documents
Kinetics and Mechanism of Bromine Addition to Derivatives of Unsaturated Aliphatic Carboxylic Acids in Aqueous Solution
Mohamed Farook, Syed Ahamed,Viswanathan, Seshaiyer,Ganesan, Ramachandran
, p. 1394 - 1400 (2007/10/02)
This paper deals with the kinetics of bromine addition to unsaturated compounds in presence of added bromide ions at 22, 30, 38, 46, and 54 deg C.The substrates used were acrylamide (AAm), methyl acrylate (MA), ethyl acrylate (EA), butyl acrylate (BA), t-butyl acrylate (tBA), methacrylamide (MAAm), methyl methacrylate (MMA), ethyl methacrylate (EMA), methyl crotonate (MC), and ethyl crotonate (EC).The kinetics was followed potentiometrically.The activation parameters (ΔH*, ΔS*, and ΔG*) were calculated and compared.Estimation of product ratio of bromohydrin to dibromide showed the absence of any correlation of the product formation with reactivity of the substrates.The observed parameters are discussed in relation to the proposed reaction mechanisms.
