Weight | 134.182 g/mol |
---|---|
Formula | C8H10N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
1,2,3,4-Tetrahydroquinoxaline (3476-89-9)
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- Enantioselective Hydrogenation of 2-Methylquinoxaline to ()-(2S)-2-Methyl-1,2,3,4-tetrahydroquinoxaline by Iridium Catalysis (Organometallics, 1998)
- Novel potassium channel openers. Part 4: transformation of the 1,4-benzoxazine skeleton into 1,4-benzothiazine, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroquinoxaline, indoline, and 1,5-benzoxazepine (Bioorganic & Medicinal Chemistry, 2000)
- Revised Structure for the Product from the Reaction of 3-Hydrazinocarbonylmethylene-2-oxo-1, 2, 3, 4-tetrahydroquinoxaline with Nitrous Acid (Chemical & Pharmaceutical Bulletin, 1984)
- Inter- and intramolecular Mitsunobu reaction and metal complexation study: synthesis of S-amino acids derived chiral 1,2,3,4-tetrahydroquinoxaline, benzo-annulated [9]-N3 peraza, [12]-N4 peraza-macrocycles (Organic and Biomolecular Chemistry, 2012)
- Quinoxaline Studies. IV. The Preparation of dl-2,6-Dimethyl-1,2,3,4-tetrahydroquinoxaline and dl-2,7-Dimethyl-1,2,3,4-tetrahydroquinoxaline (Journal of the American Chemical Society, 1952)
- Quinoxaline studies. XVI. Unequivocal synthesis of (S)-2-methyl-1,2,3,4-tetrahydroquinoxaline (Journal of Organic Chemistry, 1970)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CNC2=CC=CC=C2N1
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InChIKeyHORKYAIEVBUXGM-UHFFFAOYSA-N
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