| Weight | 134.182 g/mol |
|---|---|
| Formula | C8H10N2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5,6,7,8-tetrahydro-1,6-naphthyridine (80957-68-2)
80957-68-2
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- Methods for the synthesis of 5,6,7,8-tetrahydro-1,8-naphthyridine fragments for V3 integrin antagonists (Journal of Organic Chemistry, 2004)
- ITH4012 (Ethyl 5-Amino-6,7,8,9-tetrahydro-2-methyl-4-phenylbenzol[1,8]naphthyridine-3-carboxylate), a Novel Acetylcholinesterase Inhibitor with Calcium Promotor and Neuroprotective Properties (Journal of Pharmacology and Experimental Therapeutics, 2004)
- Ready access to 7,8-dihydro- and 1,2,3,4-tetrahydro-1,6-naphthyridine-5(6H)-ones from simple pyridine precursors (Journal of Heterocyclic Chemistry, 2006)
- Antivertigo Agents. III. Synthesis of 5, 6, 7, 8-Tetrahydro-1, 6-naphthyridine Methyl Homologs (Chemical & Pharmaceutical Bulletin, 1984)
- A FACILE SYNTHESIS OF THE 3-AMINO-5,6,7,8-TETRAHYDRO[1,6]NAPHTHYRIDINE SYSTEM AND SOME ALKYLATED AND POLYCYCLIC HOMOLOGUES (Synthetic Communications, 2001)
- New heterocyclic systems based on 1-hydrazino-5,6,7,8-tetrahydro[2,7]naphthyridine: 7,8,9,10-tetra-hydro[1,2,4]triazolo[3,4-a]- and 7,8,9,10-tetra-hydro[1,2,4]triazolo[5,1-a][2,7]naphthyridines (Chemistry of Heterocyclic Compounds, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 80957-68-2
-
SMILESC1CNCC2=C1N=CC=C2
-
InChIKeyFPEAARFNXIWCTP-UHFFFAOYSA-N
Suppliers
Most-cited Publications
Safety
Alternate Names
Estimated Properties
| Boiling Point | 241.58 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 241.14 C | EPI Suite |
| Density | 1.07 g/cm3 | EPA T.E.S.T. |
| Flash Point | 103.08 C | EPA T.E.S.T. |
| Melting Point | 55.59 C | EPI Suite |
| Water Solubility | 28351.2 mg/L | EPA T.E.S.T. |
| Water Solubility | 1e+06 mg/L | EPI Suite |
External Links
Synthesis
Reactant
+
3-(Aminomethyl)pyridine
(Reductive amination)
2-(2-Aminoethyl)pyridine
+
Reactant
(Alkylation of primary amines)
Reactant
+
CID 5477082
(Chan-Lam coupling reaction)
Similar Compounds
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(6304-27-4)
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(1609399-80-5)
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[(5,6-dimethyl-3-pyridinyl)methyl]amine dihydrochloride
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(1269198-98-2)
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6-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine dihydrochloride
(108989-52-2)
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(533-37-9)
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(873407-11-5)
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33611-48-2
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Ambcb9032118
(1048664-75-0)
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(2706-56-1)
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(19363-94-1)
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2-(azetidin-3-yl)pyridine dihydrochloride
(206446-45-9)
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(2-morpholin-4-yl-2-pyridin-3-ylethyl)amine
(410544-52-4)
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[2-(1H-indol-3-yl)ethyl](3-pyridinylmethyl)amine hydrobromide
(1609409-22-4)
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418782-49-7
(418782-49-7)
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135481-57-1
(135481-57-1)
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(874814-64-9)
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3-Ethyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine dihydrochloride
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AC1LIYMD
(869942-14-3)
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Ambcb9019031
(1048673-58-0)
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(2-phenylethyl)(pyridin-2-ylmethyl)amine
(418776-49-5)
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(1-methyl-2-pyridin-2-ylethyl)amine
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1,2,3,4-Tetrahydroisoquinoline
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[1-(5-methyl-2-pyridinyl)propyl]amine dihydrochloride
(1269384-23-7)
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20173-04-0
(20173-04-0)
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N-(2-Aminoethyl)nicotinamide
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n-(2-amino-ethyl)-nicotinamide dihydrochloride
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1-(6-Methylpyridin-2-yl)propan-2-amine
(71271-62-0)
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5,6,7,8-tetrahydro-1,6-naphthyridine
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