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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)-

1,4-Oxazepine, hexahydro-, hydrochloride

C1CNCCOC1.Cl Request for Quotation
Chemical Name: 1,4-Oxazepine, hexahydro-, hydrochloride
CAS Number: 178312-62-4
Product Number: AG0025X2(AGN-PC-03YNWE)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO
Molecular Weight: 137.6079

Identification/Properties

Properties
MP:
156-154 °C
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
137.607g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
137.061g/mol
Monoisotopic Mass:
137.061g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
47.3
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Oxazepane hydrochloride, also known as oxazepane HCl, is a versatile chemical compound extensively utilized in chemical synthesis processes. This compound serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. In the realm of organic synthesis, 1,4-Oxazepane hydrochloride acts as a key intermediate in the production of complex organic molecules with diverse functionalities. Its unique molecular structure provides opportunities for chemists to introduce specific functional groups and chiral centers, making it a valuable tool in the synthesis of biologically active compounds and sophisticated materials. By integrating 1,4-Oxazepane hydrochloride into synthetic routes, chemists can achieve precise control over the stereochemistry and reactivity of the final products, enabling the development of novel chemical entities with potential applications in the pharmaceutical and chemical industries.