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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-(hydroxymethyl)pyridin-3-yl]methanol;hydrochloride

OCc1ncccc1CO.Cl Request for Quotation
Chemical Name: [2-(hydroxymethyl)pyridin-3-yl]methanol;hydrochloride
CAS Number: 423169-40-8
Product Number: AG0072Q2(AGN-PC-01LRA4)
Synonyms:
MDL No:
Molecular Formula: C7H10ClNO2
Molecular Weight: 175.6128

Identification/Properties

Computed Properties
Molecular Weight:
175.612g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
175.04g/mol
Monoisotopic Mass:
175.04g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
97.6
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:
2
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

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Chemical Structure


Pyridine-2,3-diyldimethanol hydrochloride, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules and pharmaceutical intermediates. With its unique structure and reactivity, $name$ plays a crucial role in the formation of complex organic structures through multi-step chemical reactions. Its applications range from the synthesis of specialized polymers to the production of advanced materials in the pharmaceutical industry. By incorporating $name$ into chemical reactions, chemists can efficiently construct diverse molecular architectures with tailored properties and functionalities.