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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-methyl-1,3,4-oxadiazol-2-yl)methanol

Cc1nnc(o1)CO Request for Quotation
Chemical Name: (5-methyl-1,3,4-oxadiazol-2-yl)methanol
CAS Number: 915924-37-7
Product Number: AG00GTOF(AGN-PC-02O7UY)
Synonyms:
MDL No:
Molecular Formula: C4H6N2O2
Molecular Weight: 114.1026

Identification/Properties

Properties
BP:
248.2°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
114.104g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
114.043g/mol
Monoisotopic Mass:
114.043g/mol
Topological Polar Surface Area:
59.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
78.4
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


The compound 5-Methyl-1,3,4-oxadiazol-2-yl)methanol plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, it serves as a valuable intermediate in the preparation of various organic compounds. This compound can be utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science applications. Its functional groups allow for easy modification and derivatization, enabling the creation of diverse and complex molecules. Whether it is in the development of new drugs or the design of advanced materials, the application of (5-Methyl-1,3,4-oxadiazol-2-yl)methanol in chemical synthesis offers limitless possibilities for innovation and discovery.