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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)-

Benzene, 1-bromo-3-(2-bromoethyl)-

BrCCc1cccc(c1)Br Request for Quotation
Chemical Name: Benzene, 1-bromo-3-(2-bromoethyl)-
CAS Number: 40422-70-6
Product Number: AG003J4T(AGN-PC-0015YM)
Synonyms:
MDL No:
Molecular Formula: C8H8Br2
Molecular Weight: 263.9571

Identification/Properties

Properties
BP:
77-78°C at 0.1 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
263.96g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
263.897g/mol
Monoisotopic Mass:
261.899g/mol
Topological Polar Surface Area:
0A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
93.3
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:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Bromo-3-(2-bromoethyl)benzene is a versatile chemical compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in the production of various organic molecules through its unique reactivity and structural features. In chemical synthesis, it is commonly used as a precursor for the synthesis of complex organic compounds, especially in the pharmaceutical and agrochemical industries.Due to the presence of two bromine atoms on the benzene ring, 1-Bromo-3-(2-bromoethyl)benzene undergoes various substitution and coupling reactions to introduce different functional groups. These reactions allow chemists to modify the structure of the molecule and create new compounds with specific properties and activities. Additionally, the presence of an ethyl group between the bromine atoms provides a flexible linker that can be further functionalized to introduce additional functionalities.Overall, the versatility and reactivity of 1-Bromo-3-(2-bromoethyl)benzene make it a valuable tool in organic synthesis, enabling chemists to access a diverse range of compounds for various applications in the field of chemistry and beyond.