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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-Dioxane-2-methanamine, N-methyl-, hydrochloride (1:1)

CNCC1COCCO1.Cl Request for Quotation
Chemical Name: 1,4-Dioxane-2-methanamine, N-methyl-, hydrochloride (1:1)
CAS Number: 918621-33-7
Product Number: AG00H2ZZ(AGN-PC-09QBPD)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO2
Molecular Weight: 167.6339

Identification/Properties

Computed Properties
Molecular Weight:
167.633g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
167.071g/mol
Monoisotopic Mass:
167.071g/mol
Topological Polar Surface Area:
30.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
77.5
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(1,4-Dioxan-2-yl)-N-methylmethanamine hydrochloride plays a crucial role in chemical synthesis as a versatile building block. Due to its unique structure and properties, this compound is commonly employed in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its incorporation into synthetic routes facilitates the introduction of a methylmethylamine moiety, which serves as a key functional group in the design and production of target molecules. The hydrochloride salt form enhances the compound's solubility and stability, making it an ideal reagent for organic reactions. By utilizing 1-(1,4-Dioxan-2-yl)-N-methylmethanamine hydrochloride in chemical synthesis, researchers and chemists can efficiently access a range of complex compounds with diverse applications and biological activities.