1. Home
  2. Benzenemethanamine, 2-(4-morpholinylmethyl)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Benzenemethanamine, 2-(4-morpholinylmethyl)-

NCc1ccccc1CN1CCOCC1 Request for Quotation
Chemical Name: Benzenemethanamine, 2-(4-morpholinylmethyl)-
CAS Number: 91271-82-8
Product Number: AG00GUBR(AGN-PC-0LK93M)
Synonyms:
MDL No:
Molecular Formula: C12H18N2O
Molecular Weight: 206.2841

Identification/Properties

Properties
BP:
318.4 °C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
206.289g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
206.142g/mol
Monoisotopic Mass:
206.142g/mol
Topological Polar Surface Area:
38.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
181
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Morpholin-4-ylmethylbenzylamine, also known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. In organic synthesis, it serves as a valuable building block for the construction of various complex molecules due to its ability to participate in a range of important chemical reactions.One of the key applications of 2-Morpholin-4-ylmethylbenzylamine in chemical synthesis is as a primary amine in the formation of amide linkages. This compound can undergo amide formation reactions with carboxylic acids or acid chlorides, leading to the formation of amide bonds. These amide linkages are vital in the synthesis of peptides, pharmaceuticals, and various organic compounds.Additionally, 2-Morpholin-4-ylmethylbenzylamine can also act as a nucleophilic reagent in various transformations, such as nucleophilic substitution and addition reactions. Its morpholine moiety can serve as a nucleophile, attacking electrophilic centers in organic molecules to introduce new functional groups or stereochemistry.Furthermore, this compound can be employed in the synthesis of heterocyclic compounds, such as benzimidazoles, benzothiazoles, and other nitrogen-containing rings. These heterocycles are prevalent in pharmaceuticals, agrochemicals, and materials science, making 2-Morpholin-4-ylmethylbenzylamine a valuable starting material for their preparation.Overall, the versatile nature of 2-Morpholin-4-ylmethylbenzylamine makes it a valuable asset in chemical synthesis, enabling the construction of diverse organic molecules with various functionalities and applications.