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Technology Process of 1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone

1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone

Base Information
  • Chemical Name:1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone
  • CAS No.:81241-99-8
  • Molecular Formula:C20H25 N3 O2
  • Molecular Weight:339.44
  • Hs Code.:
  • European Community (EC) Number:617-207-2
  • Mol file:81241-99-8.mol
1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone

Synonyms:1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone;81241-99-8;1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, 2-(4-methoxyphenyl)-2-methylhydrazone;(2S)-2-{(E)-[(4-Methoxyphenyl)(methyl)hydrazono]methyl}-1,3,3-trimethyl-2-indolinol;1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-,(4-methoxyphenyl)methylhydrazone

Suppliers and Price of 1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of 1H-Indole-2-carboxaldehyde, 2,3-dihydro-2-hydroxy-1,3,3-trimethyl-, (4-methoxyphenyl)methylhydrazone
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:500.895°C at 760 mmHg 
  • Flash Point:256.733°C 
  • PSA：48.30000 
  • Density:1.111g/cm3 
  • LogP:3.29840 
  • XLogP3:4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:339.19467705
  • Heavy Atom Count:25
  • Complexity:487
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1(C2=CC=CC=C2N(C1(C=NN(C)C3=CC=C(C=C3)OC)O)C)C
  • Isomeric SMILES:CC1(C2=CC=CC=C2N([C@]1(/C=N/N(C)C3=CC=C(C=C3)OC)O)C)C
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