1-METHYL-1H-INDOLE-5-CARBALDEHYDE

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CAS:90923-75-4
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CAS:90923-75-4
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1-METHYL-1H-INDOLE-5-CARBALDEHYDE Basic information
Product Name:1-METHYL-1H-INDOLE-5-CARBALDEHYDE
Synonyms:1-methyl-1H-indole-5-carbaldehyde(SALTDATA: FREE);5-Formyl-1-methyl-1H-indole;1-Methylindolecarbaldehyde;1-Methyl-1H-indole-5-carboxaldehyde97%;1-Methylindole-5-carboxaldehyde;1-METHYL-1H-INDOLE-5-CARBOXALDEHYDE;1-METHYL-1H-INDOLE-5-CARBALDEHYDE;1H-Indole-5-carboxaldehyde, 1-methyl- (9CI)
CAS:90923-75-4
MF:C10H9NO
MW:159.18
EINECS:
Product Categories:ALDEHYDE
Mol File:90923-75-4.mol
1-METHYL-1H-INDOLE-5-CARBALDEHYDE Structure
1-METHYL-1H-INDOLE-5-CARBALDEHYDE Chemical Properties
Melting point 84-85.5
Boiling point 318.7±15.0 °C(Predicted)
density 1.10±0.1 g/cm3(Predicted)
storage temp. 2-8°C
form Solid
AppearanceOff-white to light yellow Solid
Sensitive Air & Moisture Sensitive
InChIInChI=1S/C10H9NO/c1-11-5-4-9-6-8(7-12)2-3-10(9)11/h2-7H,1H3
InChIKeyXIVDZBIBWGQOTI-UHFFFAOYSA-N
SMILESN1(C)C2=C(C=C(C=O)C=C2)C=C1
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 26-36
WGK Germany 3
Hazard Note Harmful
HazardClass IRRITANT
HS Code 2933998090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
1-METHYL-1H-INDOLE-5-CARBALDEHYDE Usage And Synthesis
Synthesis
Indole-5-carboxaldehyde

1196-69-6

Iodomethane

74-88-4

1-METHYL-1H-INDOLE-5-CARBALDEHYDE

90923-75-4

To a solution of 5-indolecarboxaldehyde (1.0 g, 6.9 mmol) in N,N-dimethylformamide (DMF, 15 mL) was added sodium hydride (303 mg, 60% oil dispersion, 7.59 mmol) in one portion. The reaction mixture was stirred at room temperature for 30 minutes. Subsequently, iodomethane (1.96 g, 13.8 mmol) was added to the reaction system and the mixture was continued to stir overnight. Upon completion of the reaction, ethyl acetate (200 mL) was added to dilute the reaction mixture, and the organic phase was washed sequentially with water (3 x 20 mL) and saturated saline (25 mL). The organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated to afford 1-methyl-1H-indole-5-carbaldehyde as an orange oil (1.0 g, 91% yield). The product was characterized by 1H NMR (200 MHz, CDCl3): δ 10.05 (s, 1H), 8.09 (s, 1H), 7.90-7.80 (m, 1H), 7.35-7.15 (m, 2H), 6.85-6.80 (m, 1H), 3.95 (s, 3H).

References[1] Patent: WO2004/52890, 2004, A1. Location in patent: Page 91-92
[2] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 7, p. 2060 - 2079
[3] European Journal of Medicinal Chemistry, 2018, vol. 158, p. 167 - 183
[4] Patent: US2005/209274, 2005, A1. Location in patent: Page/Page column 27
[5] Journal of Organometallic Chemistry, 2011, vol. 696, # 5, p. 1072 - 1083
1-METHYL-1H-INDOLE-5-CARBALDEHYDE Preparation Products And Raw materials
Raw materials1H-Indole, 1-methyl-5-(2-phenylethenyl)-, (E)- (9CI)-->Indole-5-carboxaldehyde-->Iodomethane-->Dimethyl carbonate-->Sodium hydride-->N,N-Dimethylformamide
Tag:1-METHYL-1H-INDOLE-5-CARBALDEHYDE(90923-75-4) Related Product Information
Indole-5-carboxaldehyde