1. Home
  2. Benzenemethanol, 3-(4-morpholinyl)-

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)-

Benzenemethanol, 3-(4-morpholinyl)-

OCc1cccc(c1)N1CCOCC1 Request for Quotation
Chemical Name: Benzenemethanol, 3-(4-morpholinyl)-
CAS Number: 145127-38-4
Product Number: AG001KLM(AGN-PC-0LX5CK)
Synonyms:
MDL No: MFCD07772812
Molecular Formula: C11H15NO2
Molecular Weight: 193.2423

Identification/Properties

Properties
BP:
379.6±42.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
193.246g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
193.11g/mol
Monoisotopic Mass:
193.11g/mol
Topological Polar Surface Area:
32.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
169
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The application of 3-Morpholinobenzyl Alcohol in chemical synthesis is widely recognized for its versatile properties and utility in various reactions. As a key intermediate in organic synthesis, this compound serves as a crucial building block for the preparation of diverse pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure enables it to participate in a range of transformations, including esterifications, amidations, and cycloadditions, making it a valuable reagent in the synthesis of complex molecules. Additionally, 3-Morpholinobenzyl Alcohol exhibits excellent chiral induction capabilities, allowing for the enantioselective synthesis of optically active compounds. Furthermore, its mild reaction conditions and compatibility with a variety of functional groups make it a preferred choice for chemists seeking efficient and robust methods for the construction of intricate molecular architectures.