dibromo(chloro)acetaldehyde

Base Information

Chemical Name:dibromo(chloro)acetaldehyde
CAS No.:64316-11-6
Molecular Formula:C2H Br2 Cl O
Molecular Weight:236.29
Hs Code.:

Synonyms:Acetaldehyde,dibromochloro- (9CI); Chlorodibromoacetaldehyde; Dibromochloroacetaldehyde

Suppliers and Price of dibromo(chloro)acetaldehyde

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Chlorodibromoacetaldehyde(>90%)
50mg
$ 135.00

Total 5 raw suppliers

Chemical Property of dibromo(chloro)acetaldehyde

Chemical Property:

Vapor Pressure:9.98mmHg at 25°C
Boiling Point:129.8°C at 760 mmHg
Flash Point:32.3°C
PSA：17.07000
Density:2.444g/cm³
LogP:1.86770

Purity/Quality:

99% ^*data from raw suppliers

Chlorodibromoacetaldehyde(>90%) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of dibromo(chloro)acetaldehyde

There total 3 articles about dibromo(chloro)acetaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 473-29-0
N,N-Dichlorobenzenesulfonamide

: 598-16-3
1,1,2-tribromoethylene

: 98-10-2
benzenesulfonamide

: 64316-11-6
dibromochloroacetaldehyde

Guidance literature:: With air; Multistep reaction; 1) 85-90 deg C, 7.5 h, 2) heating;

Reference yield:

: 621-62-5
chloroacetaldehyde diethyl acetal

: 64316-11-6
dibromochloroacetaldehyde

Guidance literature:: With bromine; erst in der Kaelte und dann bei 100grad und man destilliert das erhaltene Chlordibromaldehydalkoholat, das hierbei in Aethylalkohol und Chlordibromaldehyd gespalten wird;