Weight | 144.174 g/mol |
---|---|
Formula | C6H12N2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Methyl piperazine-1-carboxylate (50606-31-0)
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- Methylated analogues of methyl (R)-4-(3,4-dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate (GR-89,696) as highly potent -receptor agonists : Stereoselective synthesis, opioid-receptor affinity, receptor selectivity, and functional studies (Journal of Medicinal Chemistry, 2001)
- [The whole body autoradiographic studies on the distribution of 14C-labelled sodium 7 beta-[(2R, 3S)-2-(4-ethyl-2, 3-dioxo-1-piperazine-carboxamido)-3-hydroxybutanamido]-7 alpha-methoxy-3-[(1-methyl-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylate (14C-T-1982) in mice]. (The Journal of Antibiotics, 1982)
- Process for preparing 2-methyl-2-hydroxypropyl piperazine-1-carboxylate compounds (1981)
- Synthesis of tert-Butyl-4-(4-amino-3-methyl-5-nitrophenyl)piperazine-1-carboxylate (Fine chemicals, 2010)
- ChemInform Abstract: Methylated Analogues of Methyl (R)-4-(3,4-Dichlorophenylacetyl)-3- (pyrrolidin-1-ylmethyl)piperazine-1-carboxylate (GR-89,696) as Highly Potent -Receptor Agonists: Stereoselective Synthesis, Opioid-Receptor Affinity, Receptor Selectivity, and Functional Studies. (ChemInform, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)N1CCNCC1
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InChIKeyZPJZSEHCMJYUPI-UHFFFAOYSA-N
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