6308-13-0 Usage
Description
2,3-dibromopropyl acetate is a chemical compound with the molecular formula C5H8Br2O2. It is a colorless liquid with a strong, sweet odor.
Used in Chemical Industry:
2,3-dibromopropyl acetate is used as a solvent for various industrial applications, providing a medium for chemical reactions to occur.
Used in Pharmaceutical Industry:
2,3-dibromopropyl acetate is used as an intermediate in the synthesis of pharmaceuticals, contributing to the production of various medications.
Used in Agrochemical Industry:
2,3-dibromopropyl acetate is used as an intermediate in the synthesis of agrochemicals, playing a role in the development of agricultural products.
Used in Environmental Management:
2,3-dibromopropyl acetate is considered a hazardous substance and is used with caution to prevent environmental contamination, particularly to aquatic organisms. Proper disposal methods are essential to minimize its harmful effects on the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6308-13-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6308-13:
(6*6)+(5*3)+(4*0)+(3*8)+(2*1)+(1*3)=80
80 % 10 = 0
So 6308-13-0 is a valid CAS Registry Number.
6308-13-0Relevant articles and documents
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Schuetz,Millard
, p. 297,299 (1959)
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REACTIONS OF HALOGEN FLUORIDES XII. REACTION OF BROMINE TRIFLUORIDE WITH BROMINE-CONTAINING ESTERS. A NEW METHOD FOR THE SYNTHESIS OF FLUOROALKYL 2-FLUOROACRYLATES
Kartashov, A. V.,Chuvatkin, N. N.,Boguslavskaya, L. S.
, p. 2243 - 2248 (2007/10/02)
Being weak Lewis bases, esters reduce the reactivity of bromine trifluoride in the substitutive fluorination of organic bromine derivatives.For this reason the rate of the reaction of bromine trifluoride with bromine-containing esters depends not only on the electronic characteristics of the substituents at the reaction center but also on the basicity of the ester.As a rule, the selectivity of the reaction increases with increase in the basicity of the ester.The reaction of bromine trifluoride or chlorine monofluoride with fluoroalkyl 2,3-dibromopropionates can be used successfully for the synthesis of monomers (fluoroalkyl 2-fluoroacrylates).
