1. Home
  2. 2-Pyridinemethanol, 5-bromo-4-chloro-

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)-

2-Pyridinemethanol, 5-bromo-4-chloro-

OCc1ncc(c(c1)Cl)Br Request for Quotation
Chemical Name: 2-Pyridinemethanol, 5-bromo-4-chloro-
CAS Number: 103971-44-4
Product Number: AG007FBJ(AGN-PC-02K52X)
Synonyms:
MDL No:
Molecular Formula: C6H5BrClNO
Molecular Weight: 222.4670

Identification/Properties

Computed Properties
Molecular Weight:
222.466g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
220.924g/mol
Monoisotopic Mass:
220.924g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
114
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The application of (5-Bromo-4-chloropyridin-2-yl)methanol in chemical synthesis is significant in the field of organic chemistry. This compound serves as a versatile building block for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for selective functionalization at the bromine and chlorine positions, enabling the creation of complex molecular structures with specific properties.In the synthesis of pharmaceutical compounds, (5-Bromo-4-chloropyridin-2-yl)methanol can be used as a key intermediate in the production of bioactive molecules such as antiviral agents, anti-inflammatory drugs, and enzyme inhibitors. The bromine and chlorine substituents provide strategic locations for further derivatization, leading to the development of novel drug candidates with improved efficacy and selectivity.Furthermore, in the agrochemical industry, this compound finds applications in the synthesis of pesticides, herbicides, and fungicides. By incorporating (5-Bromo-4-chloropyridin-2-yl)methanol into the molecular structure of agrochemical products, chemists can tailor the properties of these compounds to target specific pests or pathogens while minimizing environmental impact.Overall, the versatility of (5-Bromo-4-chloropyridin-2-yl)methanol in chemical synthesis opens up diverse pathways for the creation of valuable compounds with wide-ranging applications in the fields of medicine, agriculture, and materials science.