Structure via PubChem · Public domain (PubChem)
Burgess reagent
Sign in to saveAlso known as methyl-N-(triethylammoniumsulfonyl)carbamate
chemical compound
In the Vinony graph
Within Vinony's link graph, Burgess reagent is referenced by 17 other articles, and connects out to organic chemistry, alcohols and digital object identifier.
Vinony files it under Carbamates, Chembox having GHS data and Chembox image size set.
Its subject is documented across 11 Wikipedia language editions.
Chemical data
- Formula
- C8H18N2O4S
- Molecular weight
- 238.31 g/mol
- IUPAC name
- (1E)-1-methoxy-N-(triethylazaniumyl)sulfonylmethanimidate
- SMILES
- CC[N+](CC)(CC)S(=O)(=O)/N=C(\[O-])/OC
- InChIKey
- YSHOWEKUVWPFNR-UHFFFAOYSA-N
- XLogP
- 2
- Polar surface area
- 87.2 Ų
- H-bond donors
- 0
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 238.099
Show 5 more facts
- chemical formula
- C₈H₁₈N₂O₄S
- canonical SMILES
- CC[N+](CC)(CC)S(=O)(=O)N=C([O-])OC
- isomeric SMILES
- CC[N+](CC)(CC)S(=O)(=O)/N=C(\[O-])/OC
- Commons category
- Burgess reagent
- melting point
- 77.0
Sources (2)
via Wikidata · CC0
Connections
organic chemistry
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alcohols
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digital object identifier
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chemical formula
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alkene
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methanol
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molar mass
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bibcode
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CAS Registry Number
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chemical reagent
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PubChem
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simplified molecular input line entry specification
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Georgia Tech
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chemical nomenclature
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ChemSpider
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zwitterion
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carbamate
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International Chemical Identifier
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European Chemicals Agency
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Globally Harmonized System of Classification and Labelling of Chemicals
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