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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-Pyridinemethanol, 6-chloro-

OCc1cccc(n1)Cl Request for Quotation
Chemical Name: 2-Pyridinemethanol, 6-chloro-
CAS Number: 33674-97-4
Product Number: AG003BYU(AGN-PC-0JNGQX)
Synonyms:
MDL No: MFCD07774110
Molecular Formula: C6H6ClNO
Molecular Weight: 143.5709

Identification/Properties

Properties
BP:
251.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
143.57g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
143.014g/mol
Monoisotopic Mass:
143.014g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89.1
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(6-Chloropyridin-2-yl)methanol is a versatile compound extensively used in chemical synthesis due to its unique reactivity and functional groups. This compound serves as a vital building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its application lies in its ability to act as a nucleophile in organic reactions, enabling the formation of new carbon-carbon or carbon-heteroatom bonds. Additionally, (6-Chloropyridin-2-yl)methanol can be utilized as a precursor for the synthesis of complex molecules with diverse properties, making it an indispensable tool for researchers and chemists in the field.