Description
1-Chloroisoquinoline (CAS No. 19493-44-8) is a high-purity heterocyclic organic compound with the molecular formula C9H6ClN. This versatile chemical building block is widely used in pharmaceutical research, agrochemical development, and materials science. The compound features a chlorinated isoquinoline backbone, offering unique reactivity for nucleophilic substitution and metal-catalyzed coupling reactions. Our product is rigorously tested to ensure ≥98% purity (HPLC) and is supplied as a crystalline solid with excellent shelf stability. Ideal for use as a precursor in the synthesis of biologically active molecules, 1-chloroisoquinoline is packaged under inert atmosphere to guarantee optimal quality. Available in research quantities from 100mg to bulk scale, with custom packaging options upon request.
Properties
- CAS Number: 19493-44-8
- Complexity: 138
- IUPAC Name: 1-chloroisoquinoline
- InChI: InChI=1S/C9H6ClN/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-6H
- InChI Key: MSQCQINLJMEVNJ-UHFFFAOYSA-N
- Exact Mass: 163.0188769
- Molecular Formula: C9H6ClN
- Molecular Weight: 163.60
- SMILES: C1=CC=C2C(=C1)C=CN=C2Cl
- Topological: 12.9
- Monoisotopic Mass: 163.0188769
- Synonyms: 1-chloroisoquinoline, Isoquinoline, 1-chloro-, DTXSID60173143, NSC 170839, DTXCID9095634, 628-561-2, inchi=1/c9h6cln/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-6, 19493-44-8, 1-Chloro-isoquinoline, 1-Chloroisoquinone, chloroisoquinoline, MFCD00024134, 1-chloro isoquinoline, Isoquinoline, chloro-, 1-chlorisochinolin, NSC170839, 1-Chloroisoquinoline, 95%, SCHEMBL144590, SCHEMBL939304, SCHEMBL5656885, SCHEMBL6450446, SCHEMBL15515508, ALBB-023931, BCP08062, BBL104227, SBB059626, STL558241, AKOS003399220, AB01423, CS-W002145, FS-2246, NSC-170839, AC-23203, BP-10100, SY008071, DB-019131, C2097, ST45022775, EN300-101914, AC-907/25004869, F8885-1665
Application
1-Chloroisoquinoline serves as a key intermediate in the synthesis of pharmaceutical compounds, particularly those targeting neurological disorders. Researchers utilize this compound in palladium-catalyzed cross-coupling reactions to create novel isoquinoline derivatives. In material science, it functions as a precursor for organic semiconductors and luminescent materials. The chlorinated position offers excellent reactivity for further functionalization in medicinal chemistry applications.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (97.9%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
- STOT SE 3 (97.9%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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