3-BROMO-5-CHLOROBENZYLALCOHOL


Chemical Name: 3-BROMO-5-CHLOROBENZYLALCOHOL
CAS Number: 917562-09-5
Product Number: AG006PZA(AGN-PC-0WAG62)
Synonyms:
MDL No:
Molecular Formula: C7H6BrClO
Molecular Weight: 221.4789

Identification/Properties


Properties
BP:
297.9±25.0 °C(Predicted)
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



(3-Bromo-5-chlorophenyl)methanol, also known as BCMP, is a valuable chemical compound used in various chemical synthesis applications. This versatile compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and various fine chemicals.In organic chemistry, BCMP is commonly employed as a building block in the synthesis of complex molecules due to its unique chemical reactivity. Its functional groups allow for facile modification and transformation, making it a popular choice in the preparation of diverse organic compounds.BCMP's structural features, including the bromine and chlorine substituents on the phenyl ring, enable it to participate in a wide range of chemical reactions such as nucleophilic substitutions, Grignard reactions, and oxidative transformations. These reactions offer chemists the opportunity to create structurally diverse and biologically active molecules for various applications in the pharmaceutical and agrochemical industries. Furthermore, BCMP's ability to act as a chiral auxiliary or as a directing group in transition metal-catalyzed reactions adds to its utility in asymmetric synthesis and the construction of complex molecular architectures.Overall, the application of (3-Bromo-5-chlorophenyl)methanol in chemical synthesis is essential for advancing the fields of medicinal chemistry, materials science, and organic synthesis by providing chemists with a versatile building block for creating novel and valuable compounds.