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Diphenyl diselenide - 96%, high purity , CAS No.1666-13-3
Basic Description
Synonyms
1,2-Diphenyldiselane | Q3538196 | Diphenyl diselenide, 98% | 9ATU3Z459Q | DTXSID6061864 | 1,2-Diphenyldiselane # | A810750 | AC-11061 | InChI=1/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10 | C12H10Se2 | NSC49763 | NSC-49763 | UNII-9ATU3Z459Q | D
Specifications & Purity
≥96%
Biochemical and Physiological Mechanisms
Diphenyl diselenide inhibits δ-aminolevulinate dehydratase (δ-ALA-D) from brain, liver and kidney in vitro.
Storage Temp
Argon charged
Shipped In
Normal
Product Description
Diphenyl diselenide (Ph2Se2) is an organoselenium compound. Its crystalline structure, toxicokinetic properties,antioxidant and anti-inflammatory activities have been investigated. Its ability to reverse the oxidative brain damage and mitochondrial dysfunction induced by acetaminophen has been studied in mice. It reacts with thallium (Tl) to form TI (SePh). It participates in a four-component radical coupling to form substituted cyclopentanes.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Benzene and substituted derivatives
Alternative Parents
Organoselenium compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Monocyclic benzene moiety - Hydrocarbon derivative - Organoselenium compound - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
(phenyldiselanyl)benzene
INCHI
InChI=1S/C12H10Se2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
InChIKey
YWWZCHLUQSHMCL-UHFFFAOYSA-N
Smiles
C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
Isomeric SMILES
C1=CC=C(C=C1)[Se][Se]C2=CC=CC=C2
WGK Germany
3
RTECS
JM9152500
UN Number
3283
Molecular Weight
312.13
Beilstein
2047179
Reaxy-Rn
2047179
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2047179&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Insoluble in water, soluble in toluene
Sensitivity
Moisture &air sensitive
Boil Point(°C)
202°C/11mmHg
Melt Point(°C)
60-63°C
Molecular Weight
312.100 g/mol
XLogP3
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
3
Exact Mass
313.911 Da
Monoisotopic Mass
313.911 Da
Topological Polar Surface Area
0.000 Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
128.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Linzhi Shen, Ziwen Xiong, Zhaohui Du, Hao Wang, Wenrui Li, Zhen Zhang, Hao Wu, Changsong Zhou, Yaming Zhou, Guanghua Tang, Jing Liu, Hongmin Yang.
(2024)
Unveiling the electron-acceptor effect in selenium-doped Cu-N-C catalyst with atomically dispersed active sites for boosting Hg0 oxidation. SEPARATION AND PURIFICATION TECHNOLOGY,
334
(126078).
2.
Chengfei Liu, Banruo Xianyu, Yiheng Dai, Shuojiong Pan, Tianyu Li, Huaping Xu.
(2023)
Intracellular Hyperbranched Polymerization for Circumventing Cancer Drug Resistance. ACS Nano,
17
(12):
(11905–11913).
3.
Jianfa Chen, Chong Lin, Mengmeng Zhang, Tianxiang Jin, Yong Qian.
(2020)
Constructing Nitrogen, Selenium Co-Doped Graphene Aerogel Electrode Materials for Synergistically Enhanced Capacitive Performance. ChemElectroChem,
7
(15):
(3311-3318).
4.
Jia Liu, Xiaoning Ma, Yanping Tong, Meidong Lang.
(2019)
Syntheses of diselenide-containing dynamic polymers and their application in polymer alloys. APPLIED SURFACE SCIENCE,
467-468
(477).
5.
Shenjie Li, Daocheng Pan.
(2012)
Cu2SnSe3 and alloyed (ZnSe)x(Cu2SnSe3)1−x nanocrystals with a metastable zincblende and wurtzite structure. JOURNAL OF CRYSTAL GROWTH,
358
(38).
6.
Kewei Gu, Tingting Wang, Guowei Yang, Nan Yu, Chengchao Du, Junli Wang.
(2024)
Inorganic–Organic Hybrid Layered Semiconductor AgSePh: Quasi-Solution Synthesis, Optical Properties, and Thermolysis Behavior. INORGANIC CHEMISTRY,
63
(14):
(6465-6473).
7.
Jinlin Wang, Can Wu, Wang Zhang, Yang Zhao, Kai Ding, Jie Xiao, Xiaoyuan Zeng, Yingjie Zhang.
(2025)
Promoting polysulfide conversion by catalytic of ZnSe nanoparticles for room-temperature sodium-sulfur battery. Journal of Energy Storage,
119
(116374).
8.
Yu Qiao, Wenzhong Ma, You Zhang, Tiansheng Gao, Haicun Yang, Zheng Cao, Jing Zhong.
(2024)
Ultra-high stretchability and shape fixation rate shape memory polyurethanes based on cyclic polytetrahydrofuran molecular rings. POLYMER,
311
(127578).
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8 Citations
H2125124