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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)-

2H-1,4-Benzoxazine-2-methanol, 3,4-dihydro-

OCC1CNc2c(O1)cccc2 Request for Quotation
Chemical Name: 2H-1,4-Benzoxazine-2-methanol, 3,4-dihydro-
CAS Number: 82756-74-9
Product Number: AG008IW3(AGN-PC-0KL7KR)
Synonyms:
MDL No:
Molecular Formula: C9H11NO2
Molecular Weight: 165.1891

Identification/Properties

Computed Properties
Molecular Weight:
165.192g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
165.079g/mol
Monoisotopic Mass:
165.079g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
152
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3,4-Dihydro-2H-benzo[b][1,4]oxazin-2-yl)methanol, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties and reactivity.One of the key applications of $name$ in chemical synthesis is its role as a precursor in the formation of heterocyclic compounds. By undergoing selective chemical transformations, such as oxidation or reduction reactions, $name$ can be strategically modified to introduce specific functional groups into the resulting molecules. This ability to tailor the structure of organic compounds makes $name$ an essential component in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, the presence of the oxazin ring in $name$ offers opportunities for diversification through ring-opening reactions. These processes enable the incorporation of different substituents onto the oxazin scaffold, leading to the development of novel compounds with potentially enhanced properties or biological activities. By leveraging the reactivity of $name$ in chemical synthesis, researchers can access a wide range of structurally diverse molecules for various applications in the field of medicinal chemistry and material science.