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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)-

(3S,5S)-3,5-Dimethylmorpholine hydrochloride

C[C@H]1COC[C@@H](N1)C.Cl Request for Quotation
Chemical Name: (3S,5S)-3,5-Dimethylmorpholine hydrochloride
CAS Number: 154634-94-3
Product Number: AG007XG6(AGN-PC-0WAIDN)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO
Molecular Weight: 151.6345

Identification/Properties

Computed Properties
Molecular Weight:
151.634g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
151.076g/mol
Monoisotopic Mass:
151.076g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
66.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3S,5S)-3,5-Dimethylmorpholine hydrochloride, also known as $name$, is a versatile chemical compound widely used in chemical synthesis. It serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. With its unique structural features, (3S,5S)-3,5-Dimethylmorpholine hydrochloride plays a crucial role in promoting specific stereochemical outcomes in organic reactions. Its presence in a reaction mixture can influence the formation of chiral centers, leading to the production of enantiomerically pure compounds. This compound is particularly useful in asymmetric synthesis, where the control of stereochemistry is essential for obtaining desired optical isomers. In addition, (3S,5S)-3,5-Dimethylmorpholine hydrochloride acts as an effective catalyst or reagent in various transformations, enabling chemists to achieve complex molecular structures with high efficiency and selectivity. Its broad applicability and robust reactivity make it a valuable tool for synthetic chemists seeking to access a diverse range of chemical products.