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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)-

(3-phenyl-1,2-oxazol-5-yl)methanamine;hydrochloride

NCc1onc(c1)c1ccccc1.Cl Request for Quotation
Chemical Name: (3-phenyl-1,2-oxazol-5-yl)methanamine;hydrochloride
CAS Number: 13608-55-4
Product Number: AG009XDD(AGN-PC-06D8OA)
Synonyms:
MDL No:
Molecular Formula: C10H11ClN2O
Molecular Weight: 210.6601

Identification/Properties

Computed Properties
Molecular Weight:
210.661g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
210.056g/mol
Monoisotopic Mass:
210.056g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
157
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Phenylisoxazol-5-yl)methylamine hydrochloride is a versatile compound that finds numerous applications in chemical synthesis. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, (3-Phenylisoxazol-5-yl)methylamine hydrochloride can be used as a key intermediate in the preparation of various biologically active compounds. Its functional groups and unique structure make it an important component in the creation of novel drug candidates, particularly in the development of potential treatments for various diseases.Furthermore, this compound's reactivity and stability make it a preferred choice in the synthesis of complex organic molecules. Its presence can significantly enhance the efficiency and selectivity of various chemical reactions, ultimately leading to the streamlined production of target compounds.Overall, the (3-Phenylisoxazol-5-yl)methylamine hydrochloride plays a crucial role in chemical synthesis, enabling researchers and chemists to explore new avenues in drug discovery, material science, and other diverse fields of chemistry.