| Weight | 208.058 g/mol |
|---|---|
| Formula | C9H6BrN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
1-bromoisoquinoline (1532-71-4)
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- Reactions of 1- and 3-bromoisoquinoline with potassium amide in liquid ammonia. Nucleophilic substitution of 3-bromoisoquinoline by the ANRORC mechanism (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- Studies on Quinoline and Isoquinoline Derivatives. IX. Synthesis of Pyrrolo [1,2-b] isoquinolines from 3-Bromoisoquinoline Derivatives (Chemical & Pharmaceutical Bulletin, 1983)
- Kiloscale BuchwaldHartwig Amination: Optimized Coupling of Base-Sensitive 6-Bromoisoquinoline-1-carbonitrile with (S)-3-Amino-2-methylpropan-1-ol (Organic Process Research & Development, 2014)
- Ring fissions during reactions of aminobromoisoquinolines with potassium amide in liquid ammonia : Formation of 1-cyanoisoindole from 3-amino-4-bromoisoquinoline (Tetrahedron Letters, 1972)
- ChemInform Abstract: DIDEHYDROHETARENES PART 32, ANRORG MECHANISM PART 11, REACTIONS OF 1 AND 3BROMOISOQUINOLINE WITH POTASSIUM AMIDE IN LIQUID AMMONIA, NUCLEOPHILIC SUBSTITUTION OF 3BROMOISOQUINOLINE BY THE ANRORC MECHANISM (ChemInform, 1974)
- ChemInform Abstract: STUDIES ON QUINOLINE AND ISOQUINOLINE DERIVATIVES. IX. SYNTHESIS OF PYRROLO(1,2-B)ISOQUINOLINES FROM 3-BROMOISOQUINOLINE DERIVATIVES (ChemInform, 1983)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=CN=C2Br
-
InChIKeyYWWZASFPWWPUBN-UHFFFAOYSA-N
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Similar Compounds
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