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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)-

1,3-oxazol-2-ylmethanamine;hydrochloride

NCc1ncco1.Cl Request for Quotation
Chemical Name: 1,3-oxazol-2-ylmethanamine;hydrochloride
CAS Number: 1041053-44-4
Product Number: AG00380N(AGN-PC-080U2H)
Synonyms:
MDL No:
Molecular Formula: C4H7ClN2O
Molecular Weight: 134.5642

Identification/Properties

Computed Properties
Molecular Weight:
134.563g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
134.025g/mol
Monoisotopic Mass:
134.025g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
57.7
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


Our product, Oxazol-2-ylmethanamine hydrochloride, plays a crucial role in chemical synthesis due to its versatile applications. As a primary amine derivative, it serves as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Oxazol-2-ylmethanamine hydrochloride is commonly employed in the synthesis of pharmaceutical compounds, where its amine functionality facilitates the formation of important drug intermediates. Its presence enables selective functional group transformations, making it an essential reagent in the pharmaceutical industry.Furthermore, in the realm of agrochemicals, this compound is utilized to synthesize crop protection agents and herbicides. Its unique structure allows for the introduction of specific functional groups that enhance the efficacy of these agricultural products.In addition, Oxazol-2-ylmethanamine hydrochloride finds utility in the production of specialty chemicals used in various industries. Its ability to participate in diverse chemical reactions makes it a valuable component in the synthesis of customized chemicals for industrial applications.Overall, the application of Oxazol-2-ylmethanamine hydrochloride in chemical synthesis showcases its significance as a multifunctional reagent that contributes to the creation of a wide range of essential compounds across different sectors.