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Thymine propenal

Base Information Edit
  • Chemical Name:Thymine propenal
  • CAS No.:85394-19-0
  • Molecular Formula:C8H8N2O3
  • Molecular Weight:180.163
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20234603
  • Nikkaji Number:J1.480.979A,J783.549C
  • Wikidata:Q76386725
  • ChEMBL ID:CHEMBL176501
  • Mol file:85394-19-0.mol
Thymine propenal

Synonyms:(E)-isomer of 3-(thymin-1'-yl)-2-propenal;3-(thymin-1'-yl)-2-propenal;thymine propenal;thymine-N(1)-2-propenal;TNPP

Suppliers and Price of Thymine propenal
Supply Marketing:Edit
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
Total 4 raw suppliers
Chemical Property of Thymine propenal Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:72.19000 
  • Density:1.374g/cm3 
  • LogP:-0.07310 
  • XLogP3:-0.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:180.05349212
  • Heavy Atom Count:13
  • Complexity:317
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CN(C(=O)NC1=O)C=CC=O
  • Isomeric SMILES:CC1=CN(C(=O)NC1=O)/C=C/C=O
Technology Process of Thymine propenal

There total 8 articles about Thymine propenal 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 water; at 25 ℃; Product distribution; Mechanism; Rate constant; effect of pH;
DOI:10.1021/jo00001a011
Guidance literature:
With sodium phenyl phosphate; In [D3]acetonitrile; water-d2; at 20 ℃; Mechanism; other hydroperoxymononucleosides;
DOI:10.1021/ja00127a038
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