Weight | 147.177 g/mol |
---|---|
Formula | C9H9NO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
1,4-Dihydro-3(2H)-isoquinolinone (24331-94-0)
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- Synthesis of 3,4dihydro5[11C]methoxy1(2H)isoquinolinone as a potential tracer for poly(ADPribose) synthetase (Journal of Labelled Compounds and Radiopharmaceuticals, 2000)
- 1,4-Dihydro-3 (2H)-isoquinolinone derivatives (1976)
- Biodistribution of 3,4-dihydro-5-[11c]methoxy-1(2h)-isoquinolinone, a potential pet tracer for poly(adp-ribose) synthetase (Nuclear Medicine and Biology, 2000)
- Preparation of carbon-14 labeled 3,4-dihydro-5-methyl-1(2H)-isoquinolinone (Journal of Labelled Compounds and Radiopharmaceuticals, 1994)
- Synthesis of a new anticonvulsant labelled with 14C: 1, 4-dihydro-1-[4-(ethylaminoacetyl)-aminophenyl]-3 (2H)-isoquinolinone (Journal of Labelled Compounds and Radiopharmaceuticals, 1978)
- ChemInform Abstract: KINETIK STUDIES ON THE PREPARATION OF 1-PHENYL-1,4-DIHYDRO-3(2H)-ISOQUINOLINONE AND ITS 4-ALKYL DERIVATIVES BY MEANS OF AMIDOALKYLATION INVOLVING CYCLIZATION (ChemInform, 1973)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C2=CC=CC=C2CNC1=O
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InChIKeyMGZGPQCRWVOGFE-UHFFFAOYSA-N
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Alternate Names
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Synthesis
Reactant
+
2-Methylbenzylamine
(Schotten-Baumann amide from acid)
2-PHENYLACETAMIDE
+
Reactant
(Alkylation of primary amines)
Similar Compounds
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(14097-39-3)
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ethyl 1,2,3,4-tetrahydro-3-isoquinolinecarboxylate hydrochloride
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(dimethylamino)(2-methylphenyl)acetic acid hydrochloride
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2-(2-aminophenyl)-N,N-dimethylacetamide
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[2-(pyrrolidin-1-ylmethyl)phenyl]methanol
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Phenylacetylglycine
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