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Aklavin

Base Information
  • Chemical Name:Aklavin
  • CAS No.:60504-57-6
  • Deprecated CAS:11002-83-8
  • Molecular Formula:C30H35NO10
  • Molecular Weight:569.609
  • Hs Code.:
  • UNII:T87WN25BNW
  • DSSTox Substance ID:DTXSID30209246
  • Nikkaji Number:J17.925F
  • Wikidata:Q27105019
  • ChEMBL ID:CHEMBL3040622
  • Mol file:60504-57-6.mol
Aklavin

Synonyms:aclacinomycin;aclacinomycin B;aclacinomycin Hydrochloride;aclacinomycin M;aclacinomycin N;aclacinomycin S;aclacinomycin T;aclacinomycin X;aclacinomycin Y;aclacinomycins;MA 144 N1;MA 144 S1;siwenmycin

Suppliers and Price of Aklavin
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
  • TRC
  • Aklavine
  • 1mg
  • $ 170.00
  • American Custom Chemicals Corporation
  • AKLAVINE 95.00%
  • 5MG
  • $ 503.21
Total 6 raw suppliers
Chemical Property of Aklavin
Chemical Property:
  • Vapor Pressure:1.2E-22mmHg at 25°C 
  • Refractive Index:1.6310 (estimate) 
  • Boiling Point:734.5°C at 760 mmHg 
  • Flash Point:398°C 
  • PSA:163.06000 
  • Density:1.2894 (rough estimate) 
  • LogP:2.15830 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:6
  • Exact Mass:569.22609631
  • Heavy Atom Count:41
  • Complexity:1020
Purity/Quality:

99% *data from raw suppliers

Aklavine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1(CC(C2=C(C3=C(C=C2C1C(=O)OC)C(=O)C4=C(C3=O)C(=CC=C4)O)O)OC5CC(C(C(O5)C)O)N(C)C)O
  • Isomeric SMILES:CC[C@]1(C[C@@H](C2=C(C3=C(C=C2[C@H]1C(=O)OC)C(=O)C4=C(C3=O)C(=CC=C4)O)O)O[C@H]5C[C@@H]([C@@H]([C@@H](O5)C)O)N(C)C)O
  • Recent ClinicalTrials:Selinexor and HAAG With/Without HMA in Relapsed/Refractory Acute Leukemia (AML) Patients
Technology Process of Aklavin

There total 16 articles about Aklavin 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 5 steps
1: 11 percent / potassium carbonate / methanol / 1.75 h / 65 °C
2: trifluoroacetic acid / Ambient temperature
3: 30 percent / p-toluenesulfonic acid monohydrate / benzene / 50 °C
4: sodium methoxide / methanol / 2 h / -20 °C
5: NaBH3CN, AcOH / H2O / 1 h / Ambient temperature
With sodium methylate; sodium cyanoborohydride; potassium carbonate; toluene-4-sulfonic acid; acetic acid; trifluoroacetic acid; In methanol; water; benzene;
DOI:10.1021/ja00404a047
Guidance literature:
Multi-step reaction with 4 steps
1: trifluoroacetic acid / Ambient temperature
2: 30 percent / p-toluenesulfonic acid monohydrate / benzene / 50 °C
3: sodium methoxide / methanol / 2 h / -20 °C
4: NaBH3CN, AcOH / H2O / 1 h / Ambient temperature
With sodium methylate; sodium cyanoborohydride; toluene-4-sulfonic acid; acetic acid; trifluoroacetic acid; In methanol; water; benzene;
DOI:10.1021/ja00404a047
Guidance literature:
Multi-step reaction with 4 steps
1: trifluoroacetic acid / Ambient temperature
2: 30 percent / p-toluenesulfonic acid monohydrate / benzene / 50 °C
3: sodium methoxide / methanol / 2 h / -20 °C
4: NaBH3CN, AcOH / H2O / 1 h / Ambient temperature
With sodium methylate; sodium cyanoborohydride; toluene-4-sulfonic acid; acetic acid; trifluoroacetic acid; In methanol; water; benzene;
DOI:10.1021/ja00404a047
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