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Kasugamycin hydrochloride

Base Information Edit
  • Chemical Name:Kasugamycin hydrochloride
  • CAS No.:6980-18-3
  • Deprecated CAS:11014-57-6,12609-82-4,39080-40-5,1135443-65-0,1135443-65-0,12609-82-4
  • Molecular Formula:C14H25N3O9
  • Molecular Weight:379.367
  • Hs Code.:
  • European Community (EC) Number:606-307-1,615-014-8
  • UNII:SXA18D440T
  • DSSTox Substance ID:DTXSID2040739
  • Wikipedia:Kasugamycin
  • Wikidata:Q27289442
  • ChEMBL ID:CHEMBL3186853
  • Mol file:6980-18-3.mol
Kasugamycin hydrochloride

Synonyms:3-O-(2-amino-4((carboxyiminomethyl)amino)-2,3,4,6-tetradeoxy-alpha-D-arabino-hexopyranosyl)-D-chiroinositol;kasugamycin;kasugamycin hydrochloride;kasugamycin hydrochloride monohydrate;kasugamycin monohydrochloride;kasugamycin, phosphate salt;kasugamycin, sulfate salt

Suppliers and Price of Kasugamycin hydrochloride
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
  • Usbiological
  • Kasugamycin
  • 10g
  • $ 552.00
  • TRC
  • Kasugamycin(~70%)
  • 1g
  • $ 45.00
  • Crysdot
  • Kasugamycin 95+%
  • 1g
  • $ 455.00
  • Chemenu
  • 2-(((2R,3S,5S,6R)-5-amino-2-methyl-6-(((1S,2R,3S,4S,5S,6S)-2,3,4,5,6-pentahydroxycyclohexyl)oxy)tetrahydro-2H-pyran-3-yl)amino)-2-iminoaceticacid 95%
  • 1g
  • $ 430.00
  • Biosynth Carbosynth
  • 3-O-[2-Amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-a-D-arabino-hexopyranosyl]-D-chiro-inositol
  • 250 g
  • $ 300.00
  • Biosynth Carbosynth
  • 3-O-[2-Amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-a-D-arabino-hexopyranosyl]-D-chiro-inositol
  • 100 g
  • $ 250.00
  • Biosynth Carbosynth
  • 3-O-[2-Amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-a-D-arabino-hexopyranosyl]-D-chiro-inositol
  • 50 g
  • $ 160.00
  • Biosynth Carbosynth
  • 3-O-[2-Amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-a-D-arabino-hexopyranosyl]-D-chiro-inositol
  • 25 g
  • $ 100.00
  • Biosynth Carbosynth
  • 3-O-[2-Amino-4-[(carboxyiminomethyl)amino]-2,3,4,6-tetradeoxy-a-D-arabino-hexopyranosyl]-D-chiro-inositol
  • 10 g
  • $ 65.00
  • American Custom Chemicals Corporation
  • KASUGAMYCIN (50 MG/ML IN DISTILLED WATER) 95.00%
  • 50MG
  • $ 806.69
Total 82 raw suppliers
Chemical Property of Kasugamycin hydrochloride Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:203oC (dec) 
  • Refractive Index:1.738 
  • Boiling Point:585.9 °C at 760 mmHg 
  • PKA:-0.62±0.41(Predicted) 
  • Flash Point:308.2 °C 
  • PSA:218.81000 
  • Density:1.97 g/cm3 
  • LogP:-3.13710 
  • Hydrogen Bond Donor Count:9
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:4
  • Exact Mass:415.1357571
  • Heavy Atom Count:27
  • Complexity:532
Purity/Quality:

99% *data from raw suppliers

Kasugamycin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:Pesticides -> Fungicides
  • Canonical SMILES:CC1C(CC(C(O1)OC2C(C(C(C(C2O)O)O)O)O)N)N=C(C(=O)O)N.Cl
  • Isomeric SMILES:C[C@@H]1[C@H](C[C@@H]([C@H](O1)OC2[C@@H]([C@H](C([C@@H]([C@@H]2O)O)O)O)O)N)N=C(C(=O)O)N.Cl
  • Description Trade names: “Kasugamin,” “Kasumin” Patent: JP 42006818; BE 657659: GB 1094566. Systemic fungicide and bactericide with protective and curative action. Controls rice blast caused by Pyricularia oryzae and other rice diseases, such as bacterial grain rot, bacterial seedling blight, and bacterial brown stripe caused by Pseudomonas spp. (15). Effective on other plant diseases, e.g., leaf mold and bacterial canker in tomatoes, bean halo blight, scab on apples, Cercospora spp. leaf spot on sugar beet, and bacterial soft rot on potatoes.
  • Uses Kasugamycin is an antibiotic aminoglycoside that inhibits protein synthesis.
Technology Process of Kasugamycin hydrochloride

There total 2 articles about Kasugamycin hydrochloride 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:

Reference yield:

Guidance literature:
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