Home Other Building Blocks 1,8-Naphthosultone

1,8-Naphthosultone

CAS No.:
83-31-8
Catalog Number:
AG003DS9
Molecular Formula:
C10H6O3S
Molecular Weight:
206.2178
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%(HPLCGC)
In Stock USA
United States
$53
- +
5g
98%(HPLCGC)
In Stock USA
United States
$126
- +
25g
98%(HPLCGC)
In Stock USA
United States
$314
- +
Product Description
Catalog Number:
AG003DS9
Chemical Name:
1,8-Naphthosultone
CAS Number:
83-31-8
Molecular Formula:
C10H6O3S
Molecular Weight:
206.2178
MDL Number:
MFCD00237293
IUPAC Name:
2-oxa-3λ6-thiatricyclo[6.3.1.04,12]dodeca-1(11),4,6,8(12),9-pentaene 3,3-dioxide
InChI:
InChI=1S/C10H6O3S/c11-14(12)9-6-2-4-7-3-1-5-8(13-14)10(7)9/h1-6H
InChI Key:
IEIADDVJUYQKAZ-UHFFFAOYSA-N
SMILES:
O=S1(=O)Oc2c3c1cccc3ccc2
EC Number:
201-468-0
NSC Number:
26341
Properties
Complexity:
330  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
206.004g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
206.215g/mol
Monoisotopic Mass:
206.004g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
51.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.3  
Literature
Title Journal
Synthesis and reactivity of a bis-sultone cross-linker for peptide conjugation and [18F]-radiolabelling via unusual 'double click' approach. Organic & biomolecular chemistry 20120207
Sultone opening with [18F]fluoride: an efficient 18F-labelling strategy for PET imaging. Chemical communications (Cambridge, England) 20111107
Isolation of a sultone as an unusual acetolysis product. Carbohydrate research 20110501
4-Benzyloxy-gamma-sultone derivatives: discovery of a novel family of non-nucleoside inhibitors of human cytomegalovirus and varicella zoster virus. Journal of medicinal chemistry 20090326
Chloroalkylsulfonate ionic liquids by ring opening of sultones with organic chloride salts. Chemical communications (Cambridge, England) 20080907
Delta-sultone formation through Rh-catalyzed C-H insertion. Organic letters 20071011
Studies of the chemical selectivity of hapten, reactivity, and skin sensitization potency. 1. Synthesis and studies on the reactivity toward model nucleophiles of the (13)C-labeled skin sensitizers hex-1-ene- and hexane-1,3-sultones. Chemical research in toxicology 20010101
Studies of the chemical selectivity of hapten, reactivity, and skin sensitization potency. 2. nmr studies of the covalent binding of the (13)c-labeled skin sensitizers 2-[13C]- and 3-[13C]hex-1-ene- and 3-[13C]hexane-1,3-sultones to human serum albumin. Chemical research in toxicology 20010101
Properties