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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)-

methyl morpholine-2-carboxylate;hydrochloride

COC(=O)C1CNCCO1.Cl Request for Quotation
Chemical Name: methyl morpholine-2-carboxylate;hydrochloride
CAS Number: 937063-34-8
Product Number: AG003S11(AGN-PC-08XSRY)
Synonyms:
MDL No: MFCD17167182
Molecular Formula: C6H12ClNO3
Molecular Weight: 181.6174

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
181.616g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
181.051g/mol
Monoisotopic Mass:
181.051g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
126
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


Methyl morpholine-2-carboxylate hydrochloride is a versatile compound widely used in chemical synthesis as a key building block. With its unique chemical structure, this reagent plays a crucial role in various organic reactions, particularly in the formation of heterocyclic compounds. Due to its ability to act as a nucleophile and form stable intermediates, Methyl morpholine-2-carboxylate hydrochloride is commonly employed in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its reactivity and compatibility with a wide range of other reagents make it a valuable tool for synthetic chemists aiming to create complex molecular structures efficiently and selectively.