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15088-78-5

15088-78-5 | Disulfide, bis(phenylacetyl)

CAS No: 15088-78-5 Catalog No: AG001MX3 MDL No:MFCD00513572

Product Description

Catalog Number:
AG001MX3
Chemical Name:
Disulfide, bis(phenylacetyl)
CAS Number:
15088-78-5
Molecular Formula:
C16H14O2S2
Molecular Weight:
302.4112
MDL Number:
MFCD00513572
IUPAC Name:
S-(2-phenylacetyl)sulfanyl 2-phenylethanethioate
InChI:
InChI=1S/C16H14O2S2/c17-15(11-13-7-3-1-4-8-13)19-20-16(18)12-14-9-5-2-6-10-14/h1-10H,11-12H2
InChI Key:
IXGZXXBJSZISOO-UHFFFAOYSA-N
SMILES:
O=C(Cc1ccccc1)SSC(=O)Cc1ccccc1

Properties

Complexity:
286  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
302.044g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
302.406g/mol
Monoisotopic Mass:
302.044g/mol
Rotatable Bond Count:
7  
Topological Polar Surface Area:
84.7A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7  

Literature

Title Journal
Sulfurization of dinucleoside phosphite triesters with chiral disulfides. Nucleosides, nucleotides & nucleic acids 20110901
An alternative advantageous protocol for efficient synthesis of phosphorothioate oligonucleotides utilizing phenylacetyl disulfide (PADS). Nucleosides, nucleotides & nucleic acids 20070101
Development of siRNA for therapeutics: efficient synthesis of phosphorothioate RNA utilizing phenylacetyl disulfide (PADS). Bioorganic & medicinal chemistry letters 20060501
Solid phase synthesis of phosphorothioate oligonucleotides utilizing diethyldithiocarbonate disulfide (DDD) as an efficient sulfur transfer reagent. Nucleosides, nucleotides & nucleic acids 20030401

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