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| Targets |
1,3-Dichloroisoquinoline is a heteroaromatic building block used in the synthesis of 1,3,4-trisubstituted isoquinoline derivatives. As a synthetic intermediate, it does not have specific biological targets. The isoquinoline scaffold is a privileged structure in medicinal chemistry, found in many bioactive compounds, including alkaloids and pharmaceuticals. The two chlorine substituents provide handles for nucleophilic aromatic substitution and cross-coupling reactions. The compound's derivatives may interact with various biological targets, depending on the final functionalization.
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| ln Vitro |
In vitro, 1,3-dichloroisoquinoline is used as a biochemical reagent and organic compound for life science research. It may be used in the facile synthesis of 1,3,4-trisubstituted isoquinoline derivatives. Cellular assays are typically performed on the final compounds synthesized from this building block. The compound's dichlorinated isoquinoline scaffold allows for various chemical transformations, making it valuable for drug discovery and chemical synthesis. The compound is also used in the synthesis of various heterocyclic compounds.
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| ln Vivo |
In vivo data for 1,3-dichloroisoquinoline is limited, as it is primarily a research reagent and synthetic intermediate. The compound is classified for research use only and is not intended for human or veterinary therapeutic applications. However, isoquinoline derivatives synthesized using this intermediate may have various biological activities. The compound's primary value lies in its use as a synthetic intermediate. Specific in vivo data for the parent compound is not available in the public literature.
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| Enzyme Assay |
In vitro enzyme/receptor binding assays for 1,3-dichloroisoquinoline are not typically performed, as it is a synthetic intermediate. The compound is used as a building block in organic synthesis to prepare 1,3,4-trisubstituted isoquinoline derivatives. A typical assay involves using the compound in chemical reactions, including nucleophilic aromatic substitution and cross-coupling reactions. The compound is dissolved in organic solvents such as DMSO or ethanol. The resulting products can be evaluated for biological activity. Enzyme inhibition or receptor binding assays can be performed on the final synthesized compounds. IC₅₀ or binding affinity values are calculated from dose-response curves.
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| Cell Assay |
Cellular assays for 1,3-dichloroisoquinoline are not standard, as the compound is primarily a synthetic intermediate. The compound is used in the preparation of 1,3,4-trisubstituted isoquinoline derivatives. A typical protocol for evaluating the biological activity of synthesized compounds involves culturing appropriate cell lines in growth medium at 37°C with 5% CO₂. Cells are treated with synthesized compounds at varying concentrations. Cell viability, proliferation, or specific signaling readouts are assessed. IC₅₀ or EC₅₀ values are calculated from dose-response curves.
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| Animal Protocol |
In vivo animal studies for 1,3-dichloroisoquinoline are not standard, as it is a synthetic intermediate rather than a therapeutic candidate. The compound is classified for research use only and is not intended for human or veterinary applications. Any animal studies would typically be conducted on the final isoquinoline derivatives synthesized using this building block. These studies would evaluate efficacy, pharmacokinetics, and safety in appropriate animal models. The compound's primary value lies in its use as a synthetic intermediate.
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| ADME/Pharmacokinetics |
Pharmacokinetic data for 1,3-dichloroisoquinoline is limited, as it is primarily a research reagent. The compound has a molecular weight of 198.05 g/mol and a molecular formula of C₉H₅Cl₂N. It is a solid at room temperature and is stored at room temperature under inert gas. As a dichlorinated isoquinoline, it may undergo metabolic dehalogenation and oxidation. Specific ADME data is not available.
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| Toxicity/Toxicokinetics |
1,3-Dichloroisoquinoline is classified for research use only and is not intended for human or veterinary applications. Standard safety precautions include handling with appropriate personal protective equipment (gloves, lab coat, safety goggles) in a well-ventilated area. The compound should be stored in a dry, cool place under inert gas away from incompatible materials. Acute toxicity data is not readily available in the public literature. As with all research chemicals, appropriate laboratory safety practices should be followed. No specific LD₅₀ values or detailed toxicological profiles are available in the public domain.
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| Additional Infomation |
1,3-Dichloroisoquinoline (CAS 7742-73-6) is a biochemical reagent with the molecular formula C₉H₅Cl₂N. It is a heteroaromatic building block used in the synthesis of 1,3,4-trisubstituted isoquinoline derivatives. The compound is classified as a research-use-only compound not intended for diagnostic or therapeutic purposes. It is available from multiple commercial suppliers.
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| Molecular Formula |
C9H5CL2N
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| Molecular Weight |
198.05
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| Exact Mass |
196.979
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| CAS # |
7742-73-6
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| PubChem CID |
298625
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| Appearance |
Off-white to gray solid
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| Density |
1.4±0.1 g/cm3
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| Boiling Point |
328.7±22.0 °C at 760 mmHg
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| Melting Point |
121-122 °C(lit.)
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| Flash Point |
182.6±7.9 °C
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| Vapour Pressure |
0.0±0.7 mmHg at 25°C
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| Index of Refraction |
1.661
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| LogP |
3.31
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| Hydrogen Bond Donor Count |
0
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| Hydrogen Bond Acceptor Count |
1
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| Rotatable Bond Count |
0
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| Heavy Atom Count |
12
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| Complexity |
163
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| Defined Atom Stereocenter Count |
0
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| SMILES |
ClC1=CC2=C(C(Cl)=N1)C=CC=C2
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| InChi Key |
BRGZEQXWZWBPJH-UHFFFAOYSA-N
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| InChi Code |
InChI=1S/C9H5Cl2N/c10-8-5-6-3-1-2-4-7(6)9(11)12-8/h1-5H
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| Chemical Name |
1,3-dichloroisoquinoline
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| HS Tariff Code |
2934.99.9001
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| Storage |
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month |
| Shipping Condition |
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
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| Solubility (In Vitro) |
DMSO: ~25 mg/mL (~126.2 mM; with ultrasonication)
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| Solubility (In Vivo) |
Solubility in Formulation 1: ≥ 2.5 mg/mL (12.62 mM) (saturation unknown) in 10% DMSO + 90% Corn Oil (add these co-solvents sequentially from left to right, and one by one), Clear solution.
For example, if 1 mL of working solution is to be prepared, you can add 100 μL of DMSO stock solution (25.0 mg/mL) to 900 μL of corn oil and mix well. (Please use freshly prepared in vivo formulations for optimal results.) |
| Preparing Stock Solutions | 1 mg | 5 mg | 10 mg | |
| 1 mM | 5.0492 mL | 25.2461 mL | 50.4923 mL | |
| 5 mM | 1.0098 mL | 5.0492 mL | 10.0985 mL | |
| 10 mM | 0.5049 mL | 2.5246 mL | 5.0492 mL |
*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.
Calculation results
Working concentration： mg/mL；
Method for preparing DMSO stock solution： mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.
Method for preparing in vivo formulation:：Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O，mix and clarify.
(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
(2) Be sure to add the solvent(s) in order.
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