ChemicalBook--->CAS DataBase List--->4494-18-2

4494-18-2

4494-18-2 Structure

4494-18-2 Structure
IdentificationBack Directory
[Name]

ISOQUINOLINE-1-CARBALDEHYDE
[CAS]

4494-18-2
[Synonyms]

Isoquinaldaldehyde
1-FORMYLISOQUINOLINE
1-Isoquinolinecarbaldehyde
ISOQUINOLINE-1-CARBALDEHYDE
1-isquinolinecarboxaldehyde
1-Isoquinolinecarboxaldehyde
Isoquinoline-1-carboxaldehyde
Isoquinoline-1-carbaldehyde ,97%
ISOQUINOLINE-1-CARBALDEHYDE ISO 9001:2015 REACH
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C10H7NO
[MDL Number]

MFCD06738864
[MOL File]

4494-18-2.mol
[Molecular Weight]

157.17
Chemical PropertiesBack Directory
[Melting point ]

55-55.5 °C
[Boiling point ]

308.6±15.0 °C(Predicted)
[density ]

1.223±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[pka]

2.06±0.30(Predicted)
[Appearance]

Off-white to pink Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H302-H335-H315
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xn
[Risk Statements ]

22-36-20/21/22
[Safety Statements ]

26-36/37-24/25
[HS Code ]

29334900
Hazard InformationBack Directory
[Chemical Properties]

Yellow solid
[Synthesis]

1-METHYLISOQUINOLINE

1721-93-3

ISOQUINOLINE-1-CARBALDEHYDE

4494-18-2

1. Synthesis of 1-isoquinolinecarboxaldehyde: 1-methylisoquinoline (300 mg, 2.10 mmol) was dissolved in 1,4-dioxane (20 mL). Selenium dioxide (323 mg, 2.91 mmol) was added to the solution, followed by heating and refluxing under nitrogen protection for 1.5 hours. After completion of the reaction, it was cooled to room temperature and the reaction mixture was filtered through diatomaceous earth. The filtrate was distilled under reduced pressure to remove the solvent. The resulting residue was purified by silica gel column chromatography using n-hexane/ethyl acetate (5:1, v/v) as eluent, and the eluent grades containing the target product were collected, resulting in 1-isoquinolinecarboxaldehyde (252 mg, 77% yield) as a white solid. The structure of the product was confirmed by 1H-NMR (CDCl3) δ: 7.73-7.79 (m, 2H), 7.88-7.93 (m, 2H), 8.74-8.76 (m, 1H), 9.30-9.33 (m, 1H), 10.39 (s, 1H) and MS (ESI) m/z 158 (M++1).

[References]

[1] Patent: EP1346982, 2003, A1
[2] Bioorganic and Medicinal Chemistry, 2012, vol. 20, # 3, p. 1201 - 1212
[3] Journal of Medicinal Chemistry, 2018, vol. 61, # 7, p. 2753 - 2775
[4] Organic and Biomolecular Chemistry, 2012, vol. 10, # 6, p. 1239 - 1245
[5] Patent: CN103570683, 2018, B. Location in patent: Paragraph 0221; 0226-0228
Spectrum DetailBack Directory
[Spectrum Detail]

ISOQUINOLINE-1-CARBALDEHYDE(4494-18-2)1HNMR
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