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(+)-Integerrinecic acid

Base Information
  • Chemical Name:(+)-Integerrinecic acid
  • CAS No.:469-45-4
  • Molecular Formula:C10H16O5
  • Molecular Weight:216.234
  • Hs Code.:
  • Mol file:469-45-4.mol
(+)-Integerrinecic acid

Synonyms:(+)-Integerrinecic acid;(R-(R*,R*-(E)))-5-ethylidene-2-hydroxy-2,3-dimethylhexanedioic acid;Hexanedioic acid, 5-ethylidene-2-hydroxy-2,3-dimethyl-, (R-(R*,R*-(E)))-;469-45-4

Suppliers and Price of (+)-Integerrinecic acid
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
Total 5 raw suppliers
Chemical Property of (+)-Integerrinecic acid
Chemical Property:
  • Vapor Pressure:1.13E-10mmHg at 25°C 
  • Boiling Point:466.7°Cat760mmHg 
  • Flash Point:250.2°C 
  • PSA:94.83000 
  • Density:1.241g/cm3 
  • LogP:0.87910 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:5
  • Exact Mass:216.09977361
  • Heavy Atom Count:15
  • Complexity:294
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC=C(CC(C)C(C)(C(=O)O)O)C(=O)O
  • Isomeric SMILES:C/C=C(\C[C@@H](C)[C@](C)(C(=O)O)O)/C(=O)O
Technology Process of (+)-Integerrinecic acid

There total 15 articles about (+)-Integerrinecic acid 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:
Multi-step reaction with 3 steps
1: Et3N, 2-fluoro-1-methylpyridinium p-toluenesulfonate / CH2Cl2
2: 96 percent / LiOH*H2O / tetrahydrofuran / 0 °C
3: strong alkali
With lithium hydroxide; strong alkali; 1-methyl-2-fluoropyridinium p-toluenesulfonate; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja00322a036
Guidance literature:
Multi-step reaction with 4 steps
1: BuLi, diisopropylamine / tetrahydrofuran; hexane / 1 h / -40 - -30 °C
2: Et3N, 2-fluoro-1-methylpyridinium p-toluenesulfonate / CH2Cl2
3: 96 percent / LiOH*H2O / tetrahydrofuran / 0 °C
4: strong alkali
With lithium hydroxide; n-butyllithium; strong alkali; 1-methyl-2-fluoropyridinium p-toluenesulfonate; triethylamine; diisopropylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/ja00322a036
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