1. Home
  2. 1-Propene, 3-bromo-2-(bromomethyl)-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-Propene, 3-bromo-2-(bromomethyl)-

BrCC(=C)CBr Request for Quotation
Chemical Name: 1-Propene, 3-bromo-2-(bromomethyl)-
CAS Number: 15378-31-1
Product Number: AG003J04(AGN-PC-0NC45L)
Synonyms:
MDL No:
Molecular Formula: C4H6Br2
Molecular Weight: 213.8984

Identification/Properties

Properties
BP:
184.314 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Refractive Index:
n20/D 1.550
Computed Properties
Molecular Weight:
213.9g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
213.882g/mol
Monoisotopic Mass:
211.884g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
43.5
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2810
Hazard Statements:
H301-H318-H402-H412
Precautionary Statements:
P264-P270-P273-P280-P301+P310-P305+P351+P338-P310-P321-P330-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Bromo-2-(bromomethyl)prop-1-ene, also known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique chemical properties. This compound serves as a valuable building block for the synthesis of various organic molecules, particularly in the field of organic chemistry. One of the primary applications of 3-Bromo-2-(bromomethyl)prop-1-ene is in the preparation of complex organic compounds through multi-step synthesis processes.In chemical synthesis, 3-Bromo-2-(bromomethyl)prop-1-ene acts as a crucial intermediate that undergoes different chemical reactions to introduce specific functional groups or structural modifications into the final target molecule. Its reactivity allows for the formation of carbon-carbon and carbon-heteroatom bonds, enabling chemists to create a wide range of intricate molecular structures with tailored properties and functionalities.Furthermore, the presence of bromine atoms in the molecule enhances its versatility in cross-coupling reactions and other transformations, making it a valuable tool for synthetic chemists working on the development of novel materials, pharmaceuticals, and agrochemicals. By incorporating 3-Bromo-2-(bromomethyl)prop-1-ene into synthetic pathways, researchers can access a diverse array of organic compounds with important applications in various industries.