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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)-morpholin-3-ylmethanol hydrochloride

OC[C@H]1COCCN1.Cl Request for Quotation
Chemical Name: (S)-morpholin-3-ylmethanol hydrochloride
CAS Number: 218594-79-7
Product Number: AG0032HE(AGN-PC-0WA31D)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO2
Molecular Weight: 153.6073

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-morpholin-3-ylmethanol hydrochloride is a valuable chemical reagent commonly used in organic synthesis. Its unique structure and properties make it an important building block in the preparation of various compounds, especially in the pharmaceutical and agrochemical industries.One of the key applications of (S)-morpholin-3-ylmethanol hydrochloride in chemical synthesis is as a chiral auxiliary. Due to its chiral nature, this compound can be used to introduce chirality into molecules during reactions. By attaching the (S)-morpholin-3-ylmethanol group to a substrate, stereochemical control can be achieved, leading to the formation of enantiomerically pure products. This is particularly useful in the synthesis of pharmaceuticals and other bioactive molecules where chirality plays a crucial role in determining biological activity.Moreover, (S)-morpholin-3-ylmethanol hydrochloride can also serve as a versatile protecting group in organic synthesis. By selectively masking functional groups on a molecule with this reagent, unwanted reactions can be prevented, allowing for specific transformations to occur at other sites. Once the desired reactions are complete, the protecting group can be easily removed, revealing the original functional groups intact.Overall, the use of (S)-morpholin-3-ylmethanol hydrochloride in chemical synthesis offers chemists a powerful tool to control stereochemistry and protect functional groups, enabling the efficient and selective synthesis of complex molecules with high levels of purity and yield.