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经验公式(希尔记法):
C10H9NO
化学文摘社编号:
分子量:
159.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Segment
assay
97%
mp
81-85 °C (lit.)
functional group
aldehyde
SMILES string
Cn1c(C=O)cc2ccccc12
InChI
1S/C10H9NO/c1-11-9(7-12)6-8-4-2-3-5-10(8)11/h2-7H,1H3
InChI key
IBNGPIOSWCMJGG-UHFFFAOYSA-N
Application
1-Methylindole-2-carboxaldehyde may be used in the synthesis of indole-based melatonin analog hydrazone derivatives and (E)-5-((benzyloxy)methyl)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-3-((1-methyl-1H-indol-2-yl)methylene)dihydrofuran-2(3H)-one.
Reactant for preparation of:
- Deazapurine isosteres from acylindoles via pyridine ring annulation
- 2,4-dichlorocinnamohydroxamic acid analogs for enhancing pharmacokinetics of botulinum neurotoxin serotype A protease inhibitors
- Tetrahydrocarbazoles via organocatalytic cascade Friedel-Crafts alkylation/Michael addition/aromatization reaction
- Azides, imines and amines via flow processes of amines and trimethylsilyl azide and aza-Wittig reaction
- 3-indolylpyridinedicarbonitriles as anti-inflammatory agents
- Bis(indolyl)methanes as antimicrobial and antioxidant agents
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
