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Merck
CN

554324

二硫化二苯乙酰

96%

别名:

二苯乙酰基二硫化物, 双(苯乙酰基)二硫化物

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关于此项目

线性分子式:
(C6H5CH2COS)2
化学文摘社编号:
分子量:
302.41
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Form:
solid
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产品名称

二硫化二苯乙酰, 96%

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

SMILES string

O=C(Cc1ccccc1)SSC(=O)Cc2ccccc2

InChI key

IXGZXXBJSZISOO-UHFFFAOYSA-N

assay

96%

form

solid

mp

59-63 °C (lit.)

functional group

disulfide
phenyl

Quality Level

Application

苯乙酰二硫化物(PADS)可作为硫转移剂用于硫代磷酸寡核苷酸。

General description

苯乙酰二硫化物在磷酸盐制备过程中用作硫化试剂。苯乙硫醇磺酸盐与硫代乙酸在三乙胺的作用下反应可合成苯基乙酰二硫化物。

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

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A study on the use of phenylacetyl disulfide in the solid-phase synthesis of oligodeoxynucleoside phosphorothioates.
Roelen HCPF, et al.
J. R. Neth. Chem. Soc., 110(7-8), 325-331 (1991)
"Organic disulfides and related substances. XXIII. Unsymmetrical carbonyl disulfides and cognate compounds"
Fiel L and Buckman DJ
The Journal of Organic Chemistry, 32(11), 3467-3470 (1967)
Andreas Aemissegger et al.
Tetrahedron, 63(27), 6185-6190 (2007-07-02)
The synthesis of 1-(2-nitrophenylethyl) caged O-phosphorothioylserine, -threonine and -tyrosine derivatives is reported. These amino acid building blocks can be directly incorporated into peptides by Fmoc-based solid phase synthesis as their pentafluorophenyl esters or as symmetric anhydrides. Upon irradiation with UV
Use of phenylacetyl disulfide (PADS) in the synthesis of oligodeoxyribonucleotide phosphorothioates.
Cheruvallath ZS, et al.
Nucleosides, nucleotides & nucleic acids, 18(3), 485-492 (1999)
Honglu Zhang et al.
Journal of the American Chemical Society, 128(51), 16464-16465 (2006-12-21)
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 physiology. Control of PI 3-K and PtdIns(3,4,5)P3 levels is an important therapeutic target

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