What is the 1,3-Dibromopropane?

1,3-Dibromopropane is colourless to slightly yellow liquid, while it's Molecular Formula is C3H6Br2. colourless to slightly yellow liquid 1,3-Dibromopropane is used to prepare C3-bridged compounds through C-N coupling reactions. It is used in the preparation of 2,3,4,5-tetrahydro-7,7-diphenylimidazo- [2,1-b]-thiazine-6(7H)-one by reacting with potassium salt of 5,5-diphenyl-2-thiohydantoin.

What is the CAS number for 1,3-Dibromopropane?

The CAS number of 1,3-Dibromopropane is 109-64-8.

What is 1,3-Dibromopropane (109-64-8) used for?

1,3-Dibromopropane is a dihalogenated propane, which is a colorless to slightly yellow liquid with a sweet odor. It is soluble in ether, acetone, and chloroform, but insoluble in water. 1,3-Dibromopropane undergoes reduction catalyzed by electrogenerated solution-phase nickel(I) salen and nickel(I) salen confined in a polymer film on the surface of a carbon electrode, resulting in the formation of cyclopropane and propylene. Additionally, 1,3-dibromopropane decomposes when exposed to heat for an extended period and is partially converted to 1,2-dibromopropane. Boiling with water leads to the production of propylene glycol, and it is also used to study the substrate specificity of haloalkane dehalogenases.InChI:InChI=1/C3H6Br2/c1-3-5-11-19-15(17)13-9-7-8-10-14(13)16(18)20-12-6-4-2/h7-10H,3-6,11-12H2,1-2H3

What is the 1,3-Dibromopropane?

1,3-Dibromopropane is colourless to slightly yellow liquid, while it's Molecular Formula is C3H6Br2. colourless to slightly yellow liquid 1,3-Dibromopropane is used to prepare C3-bridged compounds through C-N coupling reactions. It is used in the preparation of 2,3,4,5-tetrahydro-7,7-diphenylimidazo- [2,1-b]-thiazine-6(7H)-one by reacting with potassium salt of 5,5-diphenyl-2-thiohydantoin.

What is the CAS number for 1,3-Dibromopropane?

The CAS number of 1,3-Dibromopropane is 109-64-8.

What is 1,3-Dibromopropane (109-64-8) used for?

1,3-Dibromopropane is a dihalogenated propane, which is a colorless to slightly yellow liquid with a sweet odor. It is soluble in ether, acetone, and chloroform, but insoluble in water. 1,3-Dibromopropane undergoes reduction catalyzed by electrogenerated solution-phase nickel(I) salen and nickel(I) salen confined in a polymer film on the surface of a carbon electrode, resulting in the formation of cyclopropane and propylene. Additionally, 1,3-dibromopropane decomposes when exposed to heat for an extended period and is partially converted to 1,2-dibromopropane. Boiling with water leads to the production of propylene glycol, and it is also used to study the substrate specificity of haloalkane dehalogenases.InChI:InChI=1/C3H6Br2/c1-3-5-11-19-15(17)13-9-7-8-10-14(13)16(18)20-12-6-4-2/h7-10H,3-6,11-12H2,1-2H3

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109-64-8

Product Name：1,3-Dibromopropane
Molecular Formula：C₃H₆Br₂
Purity：99%
Molecular Weight：201.889

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Product Details

pd_meltingpoint:-34 °C(lit.)

Appearance:colourless to slightly yellow liquid

Purity:99%

Chemical plants supply high-quality 1,3-Dibromopropane 109-64-8 in bulk

Molecular Formula:C3H6Br2
Molecular Weight:201.889
Appearance/Colour:colourless to slightly yellow liquid
Vapor Pressure:0mmHg at 25°C
Melting Point:-34 °C(lit.)
Refractive Index:n20/D 1.524(lit.)
Boiling Point:167 °C at 760 mmHg
Flash Point:54.4 °C
PSA：0.00000
Density:1.933 g/cm³
LogP:2.16630

1,3-Dibromopropane(Cas 109-64-8) Usage

Hazard	Colorless liquid; sweet odor. Insoluble in water; soluble in organic solvents. Combustible.
Synthesis	1,3-Dibromopropane can be prepared via the free radical addition between allyl bromide and hydrogen bromide. It can derived from the reaction of propylene glycol with brominated hydrochloric acid.
Purification Methods	1,3-Dibromopropane [109-64-8] M 201.9, f -34.4o, b 63 -63.5o/26mm, 76 -77o/40mm, 9 0o/80mm, 165o/atm, d 4 1.977, n 1.522. Wash the dibromide with dilute aqueous Na2CO3, then water. Dry and fractionally distil it under reduced pressure. [Beilstein 1 IV 216.]
General Description	1,3-Dibromopropane is a dihalogenated propane. It undergoes reduction catalyzed by electrogenerated solution-phase nickel(I) salen and nickel(I) salen confined in a polymer film on the surface of a carbon electrode to afford cyclopropane and propylene, respectively.