88284-48-4,MFCD00799598
Catalog No.:AA0032T9

88284-48-4 | 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$6.00   $4.00
- +
1g
95%
in stock  
$22.00   $16.00
- +
5g
≥95%
in stock  
$38.00   $27.00
- +
10g
95%
in stock  
$58.00   $41.00
- +
25g
95%
in stock  
$143.00   $100.00
- +
100g
95%
in stock  
$539.00   $378.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0032T9
Chemical Name:
2-(Trimethylsilyl)phenyl trifluoromethanesulfonate
CAS Number:
88284-48-4
Molecular Formula:
C10H13F3O3SSi
Molecular Weight:
298.3541
MDL Number:
MFCD00799598
SMILES:
O=S(=O)(C(F)(F)F)Oc1ccccc1[Si](C)(C)C
Properties
Properties
 
BP:
70 °C2 mm Hg(lit.)  
Form:
Liquid  
Refractive Index:
n20/D 1.456(lit.)  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
381  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Literature

Title: Tandem carbon-carbon bond insertion and intramolecular aldol reaction of benzyne with aroylacetones: novel formation of 4,4'-disubstituted 1,1'-binaphthols.

Journal: Chemical communications (Cambridge, England) 20121121

Title: The benzyne Fischer-indole reaction.

Journal: Organic letters 20110715

Title: 1,3-Dipolar cycloaddition of sugar azides with benzyne: a novel synthesis of 1,2,3-benzotriazolyl glycoconjugates.

Journal: Carbohydrate research 20110601

Title: Reaction of arynes with amino acid esters.

Journal: Chemical communications (Cambridge, England) 20110528

Title: Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate: a versatile precursor to o-benzyne.

Journal: The Journal of organic chemistry 20091120

Quotation Request
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SDS
Tags:88284-48-4 Molecular Formula|88284-48-4 MDL|88284-48-4 SMILES|88284-48-4 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate
Catalog No.: AA0032T9
88284-48-4,MFCD00799598
88284-48-4 | 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate
Pack Size: 250mg
Purity: 95%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 95%
in stock
$22.00 $16.00
Pack Size: 5g
Purity: ≥95%
in stock
$38.00 $27.00
Pack Size: 10g
Purity: 95%
in stock
$58.00 $41.00
Pack Size: 25g
Purity: 95%
in stock
$143.00 $100.00
Pack Size: 100g
Purity: 95%
in stock
$539.00 $378.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0032T9
Chemical Name: 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate
CAS Number: 88284-48-4
Molecular Formula: C10H13F3O3SSi
Molecular Weight: 298.3541
MDL Number: MFCD00799598
SMILES: O=S(=O)(C(F)(F)F)Oc1ccccc1[Si](C)(C)C
Properties
BP: 70 °C2 mm Hg(lit.)  
Form: Liquid  
Refractive Index: n20/D 1.456(lit.)  
Storage: Inert atmosphere;2-8℃;  
Complexity: 381  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Literature fold

Title: Tandem carbon-carbon bond insertion and intramolecular aldol reaction of benzyne with aroylacetones: novel formation of 4,4'-disubstituted 1,1'-binaphthols.

Journal: Chemical communications (Cambridge, England)20121121

Title: The benzyne Fischer-indole reaction.

Journal: Organic letters20110715

Title: 1,3-Dipolar cycloaddition of sugar azides with benzyne: a novel synthesis of 1,2,3-benzotriazolyl glycoconjugates.

Journal: Carbohydrate research20110601

Title: Reaction of arynes with amino acid esters.

Journal: Chemical communications (Cambridge, England)20110528

Title: Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate: a versatile precursor to o-benzyne.

Journal: The Journal of organic chemistry20091120

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