84739
Sulfur trioxide triethylamine complex
technical, ≥95% sulfur basis
Synonym(s):
NSC 68185, NSC 8168, Triethylamine sulfur trioxide complex
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About This Item
Linear Formula:
(CH3CH2)3N · SO3
CAS Number:
Molecular Weight:
181.25
Beilstein:
3993165
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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grade
technical
Quality Level
Assay
≥95% sulfur basis
form
powder
reaction suitability
reagent type: oxidant
mp
~85 °C
storage temp.
2-8°C
SMILES string
O=S(=O)=O.CCN(CC)CC
InChI
1S/C6H15N.O3S/c1-4-7(5-2)6-3;1-4(2)3/h4-6H2,1-3H3;
InChI key
YYHPEVZFVMVUNJ-UHFFFAOYSA-N
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Application
Reactant for reagent for synthesis of:
- Anticoagulant and antiplatelet persulfated glycosides or flavonoids containing an oligopolysulfated moiety
- Narciclasine derivatives for use as anticancer agents
- Sulfate-conjugated methylprednisolone for use as a colon-specific prodrug
- Tetrasaccharide substrates of heparanase by glycosylation of disaccharides
- Synthetic heparin oligosaccharide microarrays for analysis of heparin-protein interactions
- Dexamethasone 21-sulfate sodium for use as a colon-specific prodrug
Other Notes
Reagent used for the sulfation of alcohols and other compounds
related product
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Currently available anticoagulants for prevention and treatment of thrombosis have several limitations, thus, small organic scaffolds that can dissolve clots in vivo in a dose dependent manner with lesser side effects are highly desirable. Here we report the synthesis of
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E.E. Gilbert
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