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S-Deoxo-(R)-sparasomycin

Base Information
  • Chemical Name:S-Deoxo-(R)-sparasomycin
  • CAS No.:60484-34-6
  • Molecular Formula:C13H19N3O4S2
  • Molecular Weight:345.4377
  • Hs Code.:
  • NSC Number:250424,212568
  • ChEMBL ID:CHEMBL115026
S-Deoxo-(R)-sparasomycin

Synonyms:NSC212568;S-Deoxo-(R)-sparasomycin;CHEMBL115026;SPARSOMYCIN, S-DEOXO-(R)-;NSC250424;NSC-212568;NSC-250424;61827-17-6;60484-34-6

Suppliers and Price of S-Deoxo-(R)-sparasomycin
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 S-Deoxo-(R)-sparasomycin
Chemical Property:
  • Density:1.376g/cm3 
  • XLogP3:-0.1
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:8
  • Exact Mass:345.08169844
  • Heavy Atom Count:22
  • Complexity:506
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C(=O)NC(=O)N1)C=CC(=O)NC(CO)CSCSC
  • Isomeric SMILES:CC1=C(C(=O)NC(=O)N1)/C=C/C(=O)NC(CO)CSCSC
Technology Process of S-Deoxo-(R)-sparasomycin

There total 8 articles about S-Deoxo-(R)-sparasomycin 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 borohydride; In 1,2-dimethoxyethane; 1.) -78 deg C; 2.) room temp., 2 h;
DOI:10.1021/jo00329a027
Guidance literature:
Multi-step reaction with 6 steps
1: 73 percent / 5percent aq NaOH / H2O / 16 h / Ambient temperature
2: 63 percent / K2S2O8, AgNO3 / H2O / 1.) 90-100 deg C; 2.) room temp. 16 h
3: 40 percent / dimethylformamide / 96 h / Ambient temperature
4: 90 percent / NaOH / methanol; dioxane; H2O / 16 h / 40 °C
5: 1.) Triethylamine; 2.) Hydroxybenztriazole, DCC / DMF, room temp., 16 h
6: 63 percent / LiBH4 / 1,2-dimethoxy-ethane / 1.) -78 deg C; 2.) room temp., 2 h
With sodium hydroxide; dipotassium peroxodisulfate; lithium borohydride; benzotriazol-1-ol; silver nitrate; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo00329a027
Guidance literature:
Multi-step reaction with 5 steps
1: 63 percent / K2S2O8, AgNO3 / H2O / 1.) 90-100 deg C; 2.) room temp. 16 h
2: 40 percent / dimethylformamide / 96 h / Ambient temperature
3: 90 percent / NaOH / methanol; dioxane; H2O / 16 h / 40 °C
4: 1.) Triethylamine; 2.) Hydroxybenztriazole, DCC / DMF, room temp., 16 h
5: 63 percent / LiBH4 / 1,2-dimethoxy-ethane / 1.) -78 deg C; 2.) room temp., 2 h
With sodium hydroxide; dipotassium peroxodisulfate; lithium borohydride; benzotriazol-1-ol; silver nitrate; triethylamine; dicyclohexyl-carbodiimide; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jo00329a027
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