| Weight | 163.607 g/mol |
|---|---|
| Formula | C9H6ClN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-chloroisoquinoline (1532-91-8)
Suppliers
Most-cited Publications
- Synthesis and Reactions of Isoquinoline Derivatives II.1 Synthesis of 3-Chloroisoquinoline-4-aldehydes (Synthesis, 1988)
- Synthesis of 6-chloroisoquinoline-5,8-diones and pyrido[3,4-b]phenazine-5,12-diones and evaluation of their cytotoxicity and DNA topoisomerase II inhibitory activity (Bioorganic & Medicinal Chemistry, 2007)
- Synthesis of 1-amino-4-chloroisoquinoline. A new approach to 1-aminoisoquinoline (Journal of Heterocyclic Chemistry, 1978)
- Synthesis and reactions of isoquinolines. IV: Reactions of 3-chloroisoquinoline-4-carbaldehydes (Heterocycles, 1989)
- On the Reaction of 1-Chloroisoquinoline and 4-Chloroquinazoline with Several Ketone Carbanions (Chemical & Pharmaceutical Bulletin, 1970)
- Lanthanide perchlorate complexes of 4-chloroquinoline-1-oxide and 5-chloroisoquinoline-2-oxide (Inorganica Chimica Acta, 1987)
Alternate Names
-
SMILESC1=CC=C2C(=C1)C=NC=C2Cl
-
InChIKeyLBEQEEIDWHKVAR-UHFFFAOYSA-N
External Links
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LabBot found multiple suppliers for 
4-chloroisoquinoline
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