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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)-

(5-chloropyrimidin-2-yl)methanol

OCc1ncc(cn1)Cl Request for Quotation
Chemical Name: (5-chloropyrimidin-2-yl)methanol
CAS Number: 944902-98-1
Product Number: AG003MLV(AGN-PC-0ALQXM)
Synonyms:
MDL No: MFCD10697136
Molecular Formula: C5H5ClN2O
Molecular Weight: 144.5590

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
144.558g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
144.009g/mol
Monoisotopic Mass:
144.009g/mol
Topological Polar Surface Area:
46A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
83
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(5-Chloropyrimidin-2-yl)methanol is a versatile chemical compound commonly used in chemical synthesis processes. Its unique structure makes it particularly suitable for various applications in the field of organic chemistry. One key application of this compound is as a building block in the synthesis of pharmaceutical intermediates and active ingredients.Due to the presence of the chloropyrimidine moiety, (5-Chloropyrimidin-2-yl)methanol serves as a valuable starting material for the preparation of diverse pharmaceutical compounds. Its functional groups can be selectively modified to introduce specific functionalities required for the desired pharmacological properties. This compound can be utilized in the construction of biologically active molecules, such as antiviral agents, antibacterial drugs, and antifungal substances.Moreover, the introduction of (5-Chloropyrimidin-2-yl)methanol in chemical synthesis enables the creation of novel compounds with potential therapeutic applications. By incorporating this building block into synthetic pathways, chemists can access structurally complex molecules that exhibit promising biological activities. The versatility and reactivity of this compound make it an essential component in the development of new pharmaceuticals and research chemicals.