2-Phenylacetic dithioperoxyanhydride

Modify Date: 2024-01-02 19:33:06

2-Phenylacetic dithioperoxyanhydride Structure
2-Phenylacetic dithioperoxyanhydride structure
Common Name 2-Phenylacetic dithioperoxyanhydride
CAS Number 15088-78-5 Molecular Weight 302.411
Density 1.3±0.1 g/cm3 Boiling Point 481.1±48.0 °C at 760 mmHg
Molecular Formula C16H14O2S2 Melting Point 59-63 °C(lit.)
MSDS Chinese USA Flash Point 210.1±19.6 °C

 Names

Name Phenylacetyl disulfide
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 481.1±48.0 °C at 760 mmHg
Melting Point 59-63 °C(lit.)
Molecular Formula C16H14O2S2
Molecular Weight 302.411
Flash Point 210.1±19.6 °C
Exact Mass 302.043518
PSA 84.74000
LogP 4.68
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.638

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 2
HS Code 2930909090

 Synthetic Route

~95%

2-Phenylacetic dithioperoxyanhydride Structure

2-Phenylacetic ...

CAS#:15088-78-5

Literature: Kodomari, Mitsuo; Fukuda, Masaharu; Yoshitomi, Suehiko Synthesis, 1981 , # 8 p. 637 - 638

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2-Phenylacetic dithioperoxyanhydride Structure

2-Phenylacetic ...

CAS#:15088-78-5

Literature: Journal of Organic Chemistry, , vol. 42, # 13 p. 2224 - 2229

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2-Phenylacetic dithioperoxyanhydride Structure

2-Phenylacetic ...

CAS#:15088-78-5

Literature: Journal of the American Chemical Society, , vol. 28, p. 1459

 Customs

HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles4

More Articles
Synthesis and biological activity of PTEN-resistant analogues of phosphatidylinositol 3,4,5-trisphosphate.

J. Am. Chem. Soc. 128(51) , 16464-5, (2006)

The activation of phosphatidylinositol 3-kinase (PI 3-K) and subsequent production of PtdIns(3,4,5)P3 launches a signal transduction cascade that impinges on a plethora of downstream effects on cell p...

Synthesis of antisense oligonucleotides: Replacement of 3H-1, 2-benzodithiol-3-one 1, 1-dioxide (Beaucage reagent) with phenylacetyl disulfide (PADS) as efficient sulfurization reagent: From bench to bulk manufacture of active pharmaceutical ingredient. Cheruvallath ZS, et al.

Org. Process Res. Dev. 4(3) , 199-204, (2000)

Use of phenylacetyl disulfide (PADS) in the synthesis of oligodeoxyribonucleotide phosphorothioates. Cheruvallath ZS, et al.

Nucleosides Nucleotides Nucleic Acids 18(3) , 485-492, (1999)

 Synonyms

Bis(phenylacetyl) Disulfide
PADS
bis-phenylacetyl-disulfane
2-Phenylacetic dithioperoxyanhydride
DIPHENYLACETYL DISULFIDE
Diphenacetyldisulfid
Phenylacetyl Disulfide
PHENYLACETYL DISULPHIDE
Bis-phenylacetyl-disulfan
MFCD03453048
Dibenzyldithioperoxyanhydride
Bis-phenylacetyl-disulfid
Phenylacetyldisulfide
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