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CAS

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6308-13-0

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.

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  • 6308-13-0 Structure

  • Basic information

    1. Product Name: 2,3-dibromopropyl acetate
    2. Synonyms: 1-Propanol, 2,3-dibromo-, acetate
    3. CAS NO:6308-13-0
    4. Molecular Formula: C5H8Br2O2
    5. Molecular Weight: 259.9238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6308-13-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 263.1°C at 760 mmHg
    3. Flash Point: 112.9°C
    4. Appearance: N/A
    5. Density: 1.839g/cm3
    6. Vapor Pressure: 0.0105mmHg at 25°C
    7. Refractive Index: 1.512
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-dibromopropyl acetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-dibromopropyl acetate(6308-13-0)
    12. EPA Substance Registry System: 2,3-dibromopropyl acetate(6308-13-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6308-13-0(Hazardous Substances Data)

6308-13-0 Usage

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

Pd(0)-based synthetic approaches to 1,1-disubstituted-3,4-dimethylenecyclopentanes as intermediates in the preparation of a,a-disubstituted amino acid derivatives possessing indane and diazaindane skeletons

Loepez, Anna,Moreno-Manas, Marcial,Pleixats, Roser,Roglans, Anna

, p. 355 - 362 (2007/10/03)

A comparison is established between ethyl nitroacetate and ethyl N(diphenylmelhylene)glycinate as anionic glycine equivalents for the preparation of bicyclic or tricyclic a.adisubstituted amino acids. Palladiummediated approaches to 1.1disubstituted-3,4-di methylene cyclopentanes are presented (intramolecular reductive coupling of 2.6-dibromol.6dienes and cycloisomerization of 1.6enynes). Springer-Verlag Iberica 1997.

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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