1. Home
  2. (R)-Morpholin-3-ylmethanol hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

(R)-Morpholin-3-ylmethanol hydrochloride

OC[C@@H]1COCCN1.Cl Request for Quotation
Chemical Name: (R)-Morpholin-3-ylmethanol hydrochloride
CAS Number: 1212377-10-0
Product Number: AG0035TJ(AGN-PC-0WA2OX)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO2
Molecular Weight: 153.6073

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
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

Request for Quotation

Customer Feedback

Chemical Structure


(R)-Morpholin-3-ylmethanol hydrochloride, a versatile compound commonly employed in chemical synthesis, functions as a pivotal building block for the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a chiral synthon, facilitating the preparation of enantiomerically enriched molecules through asymmetric transformations. Its unique structural features make it an essential reagent in the development of complex organic molecules by enabling stereoselective reactions and creating diverse molecular architectures. Additionally, (R)-Morpholin-3-ylmethanol hydrochloride exhibits excellent reactivity and compatibility with a wide range of functional groups, offering chemists a reliable tool for the synthesis of intricate organic compounds with high efficiency and purity.