Taxonomic Classification

Taxonomy Tree

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	Metal aryls Organotin compounds Organic salts Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Metal aryl - Monocyclic benzene moiety - Hydrocarbon derivative - Organic salt - Organotin compound - Organometallic compound - Organic post-transition metal moeity - 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
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. DOI: 10.1186/s13321-016-0174-y

3D Structure

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Solubility	Insoluble in water, slightly soluble in ethanol, soluble in benzene, toluene, xylene, chloroform, carbon tetrachloride, etc.
Flash Point(°F)	231.8 °F
Flash Point(°C)	231 °F
Boil Point(°C)	>420°C
Melt Point(°C)	224-227°C
Molecular Weight	427.100 g/mol
XLogP3
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	0
Rotatable Bond Count	4
Exact Mass	428.059 Da
Monoisotopic Mass	428.059 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	25
Formal Charge	0
Complexity	301.000
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

Documents & Articles

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Citations of This Product

References

1. Miao Wang, Guo-Ming Weng, Ghulam Yasin, Mohan Kumar, Wei Zhao. (2020) A high-performance tin phosphide/carbon composite anode for lithium-ion batteries. DALTON TRANSACTIONS, 49 (46): (17026-17032). [PMID:33196073] [10.1039/D0DT03139A]
2. Sachin Mane, Yu-Xia Li, Xiao-Qin Liu, Lin-Bing Sun. (2019) Development of High Yielded Sn-Doped Porous Carbons for Selective CO2 Capture. ACS Sustainable Chemistry & Engineering, [PMID:] [10.1021/acssuschemeng.9b00462]
3. Xiao Wang, Yuan Gao, Wenjie Wang, Anjun Qin, Jing Zhi Sun, Ben Zhong Tang. (2016) Different amine-functionalized poly(diphenylsubstituted acetylenes) from the same precursor. Polymer Chemistry, 7 (33): (5312-5321). [PMID:] [10.1039/C6PY01175F]
4. Yu Gu, Jiahao Liu, Wei Gao, Meichen Liu, Chunwang Yi. (2024) One-pot in situ bulk polymerization of triblock copolymer PCL-b-PA6-b-PCL based on PA6 by using tetraphenyl tin. POLYMER, [PMID:] [10.1016/j.polymer.2024.126968]
5. Jiao Wang, Zhiyuan Mi, Caihong Lu, Zhenhua Han, Yuxin Wu, Xiaolong Fu, Guofang Zhang. (2024) Preparation of carbon nanotube-filled bismuth/tin green nanocomposites and their efficient catalytic activity in the thermal decomposition of ammonium perchlorate. Surfaces and Interfaces, [PMID:] [10.1016/j.surfin.2024.103866]

Solution Calculators

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Reviews

Canonical Smiles	C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
IUPAC Name	tetraphenylstannane
InChIKey	CRHIAMBJMSSNNM-UHFFFAOYSA-N
INCHI	1S/4C6H5.Sn/c41-2-4-6-5-3-1;/h41-5H;
Isomeric SMILES	C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4
WGK Germany	3
PubChem CID	61146
UN Number	3146
Molecular Weight	427.13
Beilstein	3145840
Reaxy-Rn	3145842

Tetraphenyltin - analytical standard , CAS No.595-90-4

Specifications