Name | 4-Benzylmorpholine-2-carbonitrile |
Synonyms | 2-Cyano-4-benzylmorpholine 4-Benzylmorpholine-2-carbonitrile 4-BENZYLMORPHOLINE-2-CARBONITRILE 4-Benzyl-2-Morpholinecarbonitrile 4-(Phenylmethyl)-2-morpholinecarbonitrile 2-Morpholinecarbonitrile, 4-(phenylmethyl)- |
CAS | 126645-52-1 |
InChI | InChI=1/C12H14N2O/c13-8-12-10-14(6-7-15-12)9-11-4-2-1-3-5-11/h1-5,12H,6-7,9-10H2 |
Molecular Formula | C12H14N2O |
Molar Mass | 202.25 |
Density | 1.14 |
Melting Point | 161.3℃ |
Boling Point | 343.1±42.0 °C(Predicted) |
Flash Point | 161.3°C |
Solubility | Chloroform (Slightly), Ethyl Acetate (Slightly) |
Vapor Presure | 7.2E-05mmHg at 25°C |
Appearance | Oil |
Color | vColourless |
pKa | 4.89±0.10(Predicted) |
Storage Condition | Refrigerator |
Refractive Index | 1.568 |
MDL | MFCD08751344 |
Hazard Symbols | T - Toxic |
Risk Codes | 25 - Toxic if swallowed |
Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
WGK Germany | 3 |
use | 4-benzylmorpholin-2-methanonitrile is used as an intermediate in medicine and chemical industry. Morpholine compounds are widely found in natural products and have strong biological activity. They are the pharmacophore of many drugs. The biological activity test results of the synthesized morpholine derivatives show that these derivatives have pharmacological activities such as lowering cholesterol, anti-hyperlipidemia, treating arteriosclerosis and anti-inflammatory. |
preparation | the target compound 4-benzyl morpholine -2-nitrile can be prepared by benzyl chloride reaction with morpholine -2-nitrile as the starting material or cyanide prepared from 4-benzyl morpholine -2-formaldehyde as the starting material. The synthesis reaction formula of 4-benzylmorpholine-2-methylonitrile is as follows: fig. 1 the synthesis reaction formula of 4-benzylmorpholine-2-methylonitrile |