1. Home
  2. Benzenemethanol, 2-chloro-3-fluoro-

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, 2-chloro-3-fluoro-

OCc1cccc(c1Cl)F Request for Quotation
Chemical Name: Benzenemethanol, 2-chloro-3-fluoro-
CAS Number: 96516-32-4
Product Number: AG005TVO(AGN-PC-02OSV2)
Synonyms:
MDL No:
Molecular Formula: C7H6ClFO
Molecular Weight: 160.5733

Identification/Properties

Properties
BP:
233.4±25.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
160.572g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
160.009g/mol
Monoisotopic Mass:
160.009g/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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


(2-Chloro-3-fluorophenyl)methanol, also known as $name$, is a versatile compound commonly employed in chemical synthesis. This compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and functional materials due to its unique structure and reactivity. In chemical synthesis, $name$ can be utilized as a key intermediate in the production of complex organic compounds. Its functional groups allow for selective modification and transformation, enabling chemists to craft intricate molecular structures with precision. By incorporating $name$ into synthesis routes, researchers can access diverse chemical space and develop novel compounds with potential applications in drug discovery, material science, and beyond.