Diisopropyl xanthogen disulfide
CAS No. 105-65-7
Diisopropyl xanthogen disulfide ( NSC 1339; NSC-1339; NSC1339; Isopropylxanthic disulfide )
Catalog No. M27975 CAS No. 105-65-7
Diisopropyl xanthogen disulfide can be used to synthesize a proligand for metal complexes related to the molybdenum cofactor.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 45 | Get Quote |
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10MG | 63 | Get Quote |
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25MG | 103 | Get Quote |
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50MG | 150 | Get Quote |
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100MG | 223 | Get Quote |
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500MG | 482 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameDiisopropyl xanthogen disulfide
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NoteResearch use only, not for human use.
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Brief DescriptionDiisopropyl xanthogen disulfide can be used to synthesize a proligand for metal complexes related to the molybdenum cofactor.
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DescriptionDiisopropyl xanthogen disulfide can be used to synthesize a proligand for metal complexes related to the molybdenum cofactor.
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SynonymsNSC 1339; NSC-1339; NSC1339; Isopropylxanthic disulfide
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PathwayOthers
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TargetOther Targets
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RecptorHIV
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Research Area——
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Indication——
Chemical Information
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CAS Number105-65-7
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Formula Weight238.3
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Molecular FormulaC8H14O4S2
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(C)OC(=O)SSC(=O)OC(C)C
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Epiafzelechin-(2beta...
The seeds of Vitis vinifera.
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Dihydroresveratrol
Dihydroresveratrol is a major metabolite of resveratrol that is produced by animal-associated bacteria, including the gut microbiota.Dihydroresveratrol and dihydroresveratrol monosulfate are detectable in urine.
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Nogo-66 (1-40)
Peptide fragment corresponding to residues 1 - 40 of Nogo-66, the domain of the myelin protein Nogo that inhibits axonal outgrowth. Acts as a competitive antagonist at the Nogo-66 receptor (NgR); blocks Nogo-66- and CNS myelin-induced inhibition of axonal growth, but does not reduce myelin-associated glycoprotein (MAG) inhibition of neurite outgrowth in vitro. Promotes regeneration of hemisected spinal axons and locomotor recovery following spinal injury in vivo.