Home Other Building Blocks Di-tert-butyl disulfide

Di-tert-butyl disulfide

CAS No.:
110-06-5
Catalog Number:
AG0035WK
Molecular Formula:
C8H18S2
Molecular Weight:
178.3585
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
95%
In Stock USA
United States
$32
- +
100g
95%
In Stock USA
United States
$88
- +
500g
95%
In Stock USA
United States
$350
- +
Product Description
Catalog Number:
AG0035WK
Chemical Name:
Di-tert-butyl disulfide
CAS Number:
110-06-5
Molecular Formula:
C8H18S2
Molecular Weight:
178.3585
MDL Number:
MFCD00008838
IUPAC Name:
2-(tert-butyldisulfanyl)-2-methylpropane
InChI:
InChI=1S/C8H18S2/c1-7(2,3)9-10-8(4,5)6/h1-6H3
InChI Key:
BKCNDTDWDGQHSD-UHFFFAOYSA-N
SMILES:
CC(SSC(C)(C)C)(C)C
EC Number:
203-734-1
NSC Number:
677434
Properties
Complexity:
80.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
178.085g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
178.352g/mol
Monoisotopic Mass:
178.085g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
50.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.9  
Literature
Title Journal
Reductive metalation of cyclic and acyclic pseudopeptidic bis-disulfides and back conversion of the resulting diamidato/dithiolato complexes to bis-disulfides. Inorganic chemistry 20100920
Preparation of DNA and RNA fragments containing guanine N(2)-thioalkyl tethers. Current protocols in nucleic acid chemistry 20100601
Synthesis of guanosine and deoxyguanosine phosphoramidites with cross-linkable thioalkyl tethers for direct incorporation into RNA and DNA. Nucleosides, nucleotides & nucleic acids 20091101
Synthesis of S-linked alpha(2-->9) octasialic acid via exclusive alpha S-glycosidic bond formation. Journal of the American Chemical Society 20090311
Mechanism of thiolate-disulfide interchange reactions in biochemistry. The Journal of organic chemistry 20080104
Computational rationalization of the dependence of the enantioselectivity on the nature of the catalyst in the vanadium-catalyzed oxidation of sulfides by hydrogen peroxide. Journal of the American Chemical Society 20050316
Density functional study on the mechanism of the vanadium-catalyzed oxidation of sulfides by hydrogen peroxide. The Journal of organic chemistry 20030530
Improved synthesis of tert-butanesulfinamide suitable for large-scale production. Organic letters 20030417
Enantioselective oxidation of di-tert-butyl disulfide with a vanadium catalyst: progress toward mechanism elucidation. The Journal of organic chemistry 20030110
Hydrolysis of terbufos using simulated environmental conditions: rates, mechanisms, and product analysis. Journal of agricultural and food chemistry 20011201
Enantioselective synthesis of tert-butyl tert-butanethiosulfinate catalyzed by cyclohexanone monooxygenase. Chirality 20010101
Evaluation of selected chemotypes in coupled cellular and molecular target-based screens identifies novel HIV-1 zinc finger inhibitors. Journal of medicinal chemistry 19960913
Properties