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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)-

(S)-(2-Hydroxymethyl)morpholine hydrochloride

OC[C@@H]1CNCCO1.Cl Request for Quotation
Chemical Name: (S)-(2-Hydroxymethyl)morpholine hydrochloride
CAS Number: 1313584-92-7
Product Number: AG000VZP(AGN-PC-0WA2QQ)
Synonyms:
MDL No: MFCD13191722
Molecular Formula: C5H12ClNO2
Molecular Weight: 153.6073

Identification/Properties

Computed Properties
Molecular Weight:
153.606g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
153.056g/mol
Monoisotopic Mass:
153.056g/mol
Topological Polar Surface Area:
41.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
67.4
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2S)-2-Morpholinemethanol hydrochloride, a versatile compound in chemical synthesis, plays a crucial role in various synthetic processes. Its unique properties and reactivity make it an ideal reagent for several key applications in organic chemistry. One of the primary uses of (2S)-2-Morpholinemethanol hydrochloride is as a chiral building block in the synthesis of pharmaceutical compounds. Its chirality allows for the creation of enantiomerically pure molecules, essential in drug discovery and development. By incorporating this compound into the synthesis of pharmaceutical intermediates, researchers can efficiently access new drug candidates with high levels of stereochemical control.Additionally, (2S)-2-Morpholinemethanol hydrochloride serves as a valuable protecting group in organic synthesis. Its ability to selectively block specific functional groups during complex chemical transformations enables chemists to perform intricate reactions with precision and control. By strategically incorporating this compound as a protecting group, chemists can manipulate the reactivity of other functional groups in a molecule, opening up new possibilities for synthetic pathways.Furthermore, (2S)-2-Morpholinemethanol hydrochloride can function as a catalyst or a ligand in various synthetic reactions. Its presence can facilitate key bond-forming processes, accelerate reaction rates, and improve overall yields. In complex chemical transformations, the addition of (2S)-2-Morpholinemethanol hydrochloride as a catalyst or ligand can enhance the efficiency and selectivity of the reaction, making it a valuable tool for synthetic chemists.Overall, (2S)-2-Morpholinemethanol hydrochloride stands as a versatile and indispensable reagent in chemical synthesis, offering a wide range of applications in the creation of complex molecules with defined stereochemistry and functionality. Its utility in pharmaceutical synthesis, as a protecting group, and as a catalyst highlights its significance in modern organic chemistry.