| Weight | 190.29 g/mol |
|---|---|
| Formula | C12H18N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
1-benzyl-1,4-diazepane (4410-12-2)
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- Neutral and Cationic Rare Earth Metal Alkyl and Benzyl Compounds with the 1,4,6-Trimethyl-6-pyrrolidin-1-yl-1,4-diazepane Ligand and Their Performance in the Catalytic Hydroamination/Cyclization of Aminoalkenes (Organometallics, 2008)
- Development of 6-benzyl substituted 4-aminocarbonyl-1,4-diazepane-2,5-diones as orally active human chymase inhibitors (Bioorganic & Medicinal Chemistry Letters, 2007)
- Discovery of novel series of 6-benzyl substituted 4-aminocarbonyl-1,4-diazepane-2,5-diones as human chymase inhibitors using structure-based drug design. (Bioorganic & Medicinal Chemistry, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNCCN(C1)CC2=CC=CC=C2
-
InChIKeyJTJTYCPQUOROFM-UHFFFAOYSA-N
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Synthesis
Reactant
+
N1-Benzyl-N1-methylethane-1,2-diamine
(Reductive amination)
N-(2-aminoethyl)-N-benzyl-N-ethylamine
+
Reactant
(Alkylation of primary amines)
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