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2,4,5-Trimethylthiophene-3-carbaldehyde

Base Information
  • Chemical Name:2,4,5-Trimethylthiophene-3-carbaldehyde
  • CAS No.:63826-44-8
  • Molecular Formula:C8H10OS
  • Molecular Weight:154.233
  • Hs Code.:2934999090
  • DSSTox Substance ID:DTXSID70377812
  • Wikidata:Q82167170
2,4,5-Trimethylthiophene-3-carbaldehyde

Synonyms:2,4,5-trimethylthiophene-3-carbaldehyde;63826-44-8;2,4,5-Trimethylthiophene-3-carboxaldehyde;2,3,5-Trimethylthiophene-4-carboxaldehyde;MFCD07368975;2,4,5-trimethyl-3-thiophenecarboxaldehyde;SCHEMBL11331148;DTXSID70377812;KHIVVVPWXLYVTJ-UHFFFAOYSA-N;GEO-02427;AKOS005257004;CS-0454463;FT-0609821;EN300-693139;W-200474

Suppliers and Price of 2,4,5-Trimethylthiophene-3-carbaldehyde
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Arctom
  • 2,4,5-Trimethylthiophene-3-carbaldehyde
  • 1g
  • $ 519.00
  • American Custom Chemicals Corporation
  • 2,3,5-TRIMETHYLTHIOPHENE-4-CARBOXALDEHYDE 95.00%
  • 5MG
  • $ 499.28
Total 3 raw suppliers
Chemical Property of 2,4,5-Trimethylthiophene-3-carbaldehyde
Chemical Property:
  • Vapor Pressure:0.0343mmHg at 25°C 
  • Boiling Point:242.3oC at 760 mmHg 
  • Flash Point:94.5oC 
  • PSA:45.31000 
  • Density:1.106g/cm3 
  • LogP:2.48580 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:154.04523611
  • Heavy Atom Count:10
  • Complexity:135
Purity/Quality:

97% *data from raw suppliers

2,4,5-Trimethylthiophene-3-carbaldehyde *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(SC(=C1C=O)C)C
Technology Process of 2,4,5-Trimethylthiophene-3-carbaldehyde

There total 8 articles about 2,4,5-Trimethylthiophene-3-carbaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With tin(IV) chloride; In dichloromethane; for 3h; Heating;
DOI:10.1007/BF00479334
Guidance literature:
Multi-step reaction with 3 steps
1: phosphoryl chloride / anschliessend mit wss. Natriumacetat behandeln
2: hydrazine hydrate; potassium hydroxide; ethylene glycol
3: phosphoryl chloride
With potassium hydroxide; hydrazine hydrate; ethylene glycol; trichlorophosphate;
DOI:10.1021/jo01156a016
Guidance literature:
Multi-step reaction with 3 steps
1: phosphoryl chloride / anschliessendes Behandeln mit wss. Natriumacetat
2: hydrazine hydrate; potassium hydroxide; ethylene glycol
3: phosphoryl chloride
With potassium hydroxide; hydrazine hydrate; ethylene glycol; trichlorophosphate;
DOI:10.1021/jo01156a016
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