Home Sulfos Methanesulfonic anhydride

Methanesulfonic anhydride

CAS No.:
7143-01-3
Catalog Number:
AG003RI1
Molecular Formula:
C2H6O5S2
Molecular Weight:
174.1960
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$39
- +
25g
95%
In Stock USA
United States
$47
- +
100g
95%
In Stock USA
United States
$119
- +
500g
95%
In Stock USA
United States
$443
- +
Product Description
Catalog Number:
AG003RI1
Chemical Name:
Methanesulfonic anhydride
CAS Number:
7143-01-3
Molecular Formula:
C2H6O5S2
Molecular Weight:
174.1960
MDL Number:
MFCD00007556
IUPAC Name:
methylsulfonyl methanesulfonate
InChI:
InChI=1S/C2H6O5S2/c1-8(3,4)7-9(2,5)6/h1-2H3
InChI Key:
IZDROVVXIHRYMH-UHFFFAOYSA-N
SMILES:
CS(=O)(=O)OS(=O)(=O)C
EC Number:
230-442-1
NSC Number:
65906
Properties
Complexity:
227  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
173.966g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
174.185g/mol
Monoisotopic Mass:
173.966g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
94.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.8  
Literature
Title Journal
'Greener' Friedel-Crafts acylations: a metal- and halogen-free methodology. Organic letters 20110506
Cyclopropenium-activated cyclodehydration of diols. Organic letters 20110218
Grunwald-Winstein analysis: isopropyl chloroformate solvolysis revisited. International journal of molecular sciences 20090301
Identification of stable S-adenosylmethionine (SAM) analogues derivatised with bioorthogonal tags: effect of ligands on the affinity of the E. coli methionine repressor, MetJ, for its operator DNA. Organic & biomolecular chemistry 20090221
Correlation of the rates of solvolysis of two arenesulfonyl chlorides and of trans-beta-styrenesulfonyl chloride - precursors in the development of new pharmaceuticals. International journal of molecular sciences 20081201
Concerted solvent processes for common sulfonyl chloride precursors used in the synthesis of sulfonamide-based drugs. International journal of molecular sciences 20080501
Oxidative rearrangement of indoles: a new approach to the EFHG-tetracyclic core of diazonamide A. The Journal of organic chemistry 20070413
Study of regioselective methanesulfonylation of simple aromatics with methanesulfonic anhydride in the presence of zeolite catalysts. Organic & biomolecular chemistry 20041107
Synthesis of carbonates and related compounds from carbon dioxide via methanesulfonyl carbonates. The Journal of organic chemistry 20030711
Synthesis and structure of novel 1lambda4,2,6-thiadiazines. The Journal of organic chemistry 20030516
Properties