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Cryptophycin 21

Base Information
  • Chemical Name:Cryptophycin 21
  • CAS No.:168569-15-1
  • Molecular Formula:C34H41ClN2O8
  • Molecular Weight:641.161
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401046568
  • Nikkaji Number:J833.403J
  • Wikidata:Q105100122
  • Metabolomics Workbench ID:139818
  • ChEMBL ID:CHEMBL502895
Cryptophycin 21

Synonyms:Cryptophycin 21;Cryptophycin-21;CHEMBL502895;SCHEMBL10048476;ATKRDMWWPRZLSY-BJJCRNJMSA-N;DTXSID401046568;168569-15-1

Suppliers and Price of Cryptophycin 21
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 0 raw suppliers
Chemical Property of Cryptophycin 21
Chemical Property:
  • XLogP3:5.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:8
  • Exact Mass:640.2551440
  • Heavy Atom Count:45
  • Complexity:1050
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C)CC1C(=O)OC(CC=CC(=O)NC(C(=O)NCCC(=O)O1)CC2=CC(=C(C=C2)OC)Cl)C(C)C3C(O3)C4=CC=CC=C4
  • Isomeric SMILES:C[C@@H]([C@@H]1C/C=C/C(=O)N[C@@H](C(=O)NCCC(=O)O[C@H](C(=O)O1)CC(C)C)CC2=CC(=C(C=C2)OC)Cl)[C@@H]3[C@H](O3)C4=CC=CC=C4
Technology Process of Cryptophycin 21

There total 5 articles about Cryptophycin 21 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 lithium chloride; In acetone; at 100 ℃; for 72h;
DOI:10.1021/np0499665
Guidance literature:
cryptophycin-1; With hydrogenchloride; In 1,2-dimethoxyethane; at 20 ℃; for 18h;
With potassium carbonate; In 1,2-dimethoxyethane; for 2h;
DOI:10.1021/np0499665
Guidance literature:
Multi-step reaction with 2 steps
1.1: 1.2 mg / m-chloroperbenzoic acid / CH2Cl2 / 2 h / 60 °C
2.1: aq. HCl / 1,2-dimethoxy-ethane / 18 h / 20 °C
2.2: 16 mg / K2CO3 / 1,2-dimethoxy-ethane / 2 h
With hydrogenchloride; 3-chloro-benzenecarboperoxoic acid; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1021/np0499665
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