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
登录 查看组织和合同定价。
选择尺寸
变更视图
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
Quality Level
assay
96%
form
solid
mp
59-63 °C (lit.)
functional group
disulfide, phenyl
SMILES string
O=C(Cc1ccccc1)SSC(=O)Cc2ccccc2
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
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。
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。
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)
Caged O-phosphorothioyl amino acids as building blocks for Fmoc-based solid phase peptide synthesis.
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
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)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 554324-25G | 04061832419756 |