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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)-

(2-bromo-3-chlorophenyl)methanol

OCc1cccc(c1Br)Cl Request for Quotation
Chemical Name: (2-bromo-3-chlorophenyl)methanol
CAS Number: 1232407-29-2
Product Number: AG000K83(AGN-PC-0CHGOD)
Synonyms:
MDL No: MFCD12923275
Molecular Formula: C7H6BrClO
Molecular Weight: 221.4789

Identification/Properties

Computed Properties
Molecular Weight:
221.478g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
219.929g/mol
Monoisotopic Mass:
219.929g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


2-Bromo-3-chlorobenzyl alcohol is a versatile compound that finds application in a variety of chemical synthesis processes. This compound serves as a valuable building block in the creation of complex organic molecules due to its unique reactivity and structural properties. In chemical synthesis, 2-Bromo-3-chlorobenzyl alcohol can be used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its functional groups allow for selective derivatization, enabling the introduction of specific chemical functionalities at desired positions in the molecule. Furthermore, the presence of both bromine and chlorine atoms provides opportunities for various cross-coupling reactions and substitution reactions, leading to the development of novel chemical entities with potential applications in drug discovery and material science.