1. Home
  2. Benzenemethanol, 3-chloro-a-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzenemethanol, 3-chloro-a-phenyl-

Clc1cccc(c1)C(c1ccccc1)O Request for Quotation
Chemical Name: Benzenemethanol, 3-chloro-a-phenyl-
CAS Number: 63012-03-3
Product Number: AG00E9CJ(AGN-PC-0T6V7L)
Synonyms:
MDL No:
Molecular Formula: C13H11ClO
Molecular Weight: 218.6788

Identification/Properties

Properties
BP:
342.6°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
218.68g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
218.05g/mol
Monoisotopic Mass:
218.05g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
189
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (3-Chlorophenyl)(phenyl)methanol, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure, consisting of a chlorophenyl group attached to a phenyl group connected to a methanol moiety, grants it valuable reactivity and functionality in various organic reactions.One key application of $name$ in chemical synthesis is as a building block for the construction of complex organic molecules. Its ability to undergo different chemical transformations, such as substitutions, additions, and reductions, makes it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.Additionally, $name$ can serve as a starting material for the preparation of chiral compounds. By utilizing its chiral centers and functional groups, chemists can access enantiomerically pure products important in drug discovery and asymmetric catalysis.Furthermore, the presence of the chlorophenyl group in $name$ offers opportunities for further derivatization or coupling reactions, enabling the introduction of additional functionalities or structural motifs into the final products.Overall, (3-Chlorophenyl)(phenyl)methanol plays a crucial role in advancing the field of chemical synthesis by providing chemists with a versatile and valuable building block for the creation of diverse and intricate organic molecules.