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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)-

4-(2-bromoethyl)morpholine;hydrobromide

BrCCN1CCOCC1.Br Request for Quotation
Chemical Name: 4-(2-bromoethyl)morpholine;hydrobromide
CAS Number: 42802-94-8
Product Number: AG0033SM(AGN-PC-03C6QD)
Synonyms:
MDL No: MFCD00463351
Molecular Formula: C6H13Br2NO
Molecular Weight: 274.9815

Identification/Properties

Properties
MP:
222-224℃ (methanol )
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
274.984g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
274.934g/mol
Monoisotopic Mass:
272.936g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
73.5
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


4-(2-Bromoethyl)morpholine Hydrobromide is a versatile chemical compound that finds its primary application in chemical synthesis processes. This compound serves as an essential building block in the creation of various advanced materials and pharmaceutical intermediates. In the realm of organic synthesis, it is used as a key reagent in the preparation of heterocyclic compounds and functionalized molecules. By incorporating 4-(2-Bromoethyl)morpholine Hydrobromide into reaction pathways, chemists can introduce specific functionalities and structural motifs into target molecules with precision. Its unique molecular structure imparts distinct characteristics to the products formed, making it a valuable tool for constructing complex organic frameworks. Additionally, the presence of the bromoethyl group opens up opportunities for further derivatization, enabling the synthesis of a wide range of compounds with tailored properties. Through strategic utilization in chemical transformations, 4-(2-Bromoethyl)morpholine Hydrobromide facilitates the development of novel compounds with diverse applications across various industries, including pharmaceuticals, agrochemicals, and materials science.