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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)-

8-chloro-3,4-dihydro-2H-1,4-benzoxazine

Clc1cccc2c1OCCN2 Request for Quotation
Chemical Name: 8-chloro-3,4-dihydro-2H-1,4-benzoxazine
CAS Number: 939759-05-4
Product Number: AG006AER(AGN-PC-00VAI3)
Synonyms:
MDL No:
Molecular Formula: C8H8ClNO
Molecular Weight: 169.6082

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
169.608g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
169.029g/mol
Monoisotopic Mass:
169.029g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
142
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2H-1,4-Benzoxazine, 8-chloro-3,4-dihydro- is a versatile compound widely utilized in chemical synthesis due to its unique properties. It serves as a key intermediate in the manufacturing of various pharmaceuticals, agrochemicals, and fine chemicals. This compound plays a crucial role in the synthesis of organic molecules with applications across industries such as pharmaceuticals, materials science, and agrochemicals. Its chlorinated structure imparts specific reactivity that is valuable in constructing complex molecular structures. In chemical synthesis, 2H-1,4-Benzoxazine, 8-chloro-3,4-dihydro- acts as a building block, enabling the creation of diverse compounds with tailored properties and functionalities. Its strategic use in synthesis pathways allows for the efficient production of advanced materials and compounds with high purity and specificity.