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6308-13-0

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6308-13-0 Usage

General Description

2,3-dibromopropyl acetate is a chemical compound with the molecular formula C5H8Br2O2. It is a colorless liquid with a strong, sweet odor, and is primarily used as a solvent in various industrial applications. It is also used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. The compound is considered to be toxic if ingested or inhaled, and can cause irritation to the skin and eyes. It is classified as a hazardous substance and should be handled with caution. Additionally, 2,3-dibromopropyl acetate is known to be harmful to aquatic organisms and should be disposed of properly to prevent environmental contamination.

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).

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