Cas no 36643-28-4 (Stannylium, tributyl-)
Stannylium, tributyl- structure
Product Name:Stannylium, tributyl-
CAS No:36643-28-4
MF:C12H27Sn
MW:290.052783250809
CID:309946
PubChem ID:37499
Update Time:2025-04-19
Stannylium, tributyl- Chemical and Physical Properties
Names and Identifiers
-
- Stannylium, tributyl-
- tributylstannanylium
- n-Tributyltin ion
- Tin(1+),tributyl-, ion (8CI)
- Tributylstannylium
- Tributyltin
- Tributyltin cation
- Tributyltin ion
- Tri-n-butyltin
- 36643-28-4
- Tri-n-butyltin (TBT)
- DTXSID9075030
- TRIBUTYLTIN-CATION
- BAA46123
- NS00108470
- Tin(1+), tributyl-, ion
-
- Inchi： 1S/3C4H9.Sn/c3*1-3-4-2;/h3*1,3-4H2,2H3;/q;;;+1
- InChI Key： LSKGFBJLYWXIOF-UHFFFAOYSA-N
- SMILES： [Sn+](CCCC)(CCCC)CCCC
Computed Properties
- Exact Mass: 291.113478g/mol
- Monoisotopic Mass: 291.113478g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 13
- Rotatable Bond Count: 9
- Complexity: 72.1
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 0?2
Stannylium, tributyl- Related Literature
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1. Synthesis of 1,2-fused indoles by radical cyclisation1Christopher J. Moody,Claire L. Norton Synthesis of 12-fused indoles by radical cyclisation1. Christopher J. Moody Claire L. Norton J. Chem. Soc. Perkin Trans. 1 1997 2639
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2. Tributyltin(IV) penta(methoxycarbonyl)cyclopentadienides [SnBu3L2]+-[C5(CO2Me)5]–. X-Ray crystal structure of the diaquatributyltin(IV) salt, [SnBu3(OH2)2][C5(CO2Me)5], and electron spin resonance spectrum of the radical C5(CO2Me)5Alwyn G. Davies,Jeffrey P. Goddard,Michael B. Hursthouse,Nigel P. C. Walker J. Chem. Soc. Dalton Trans. 1986 1873
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3. Radical-nucleophilic substitution (SRN1) reactions. Part 7.1 Reactions of aliphatic α-substituted nitro compounds.Suleiman I. Al-Khalil,W. Russell Bowman,Katherine Gaitonde,Madeleine A. Marley (née Nagel),Geoffrey D. Richardson J. Chem. Soc. Perkin Trans. 2 2001 1557
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Akio Takuwa,Yutaka Nishigaichi,Seiji Ebara,Hidetoshi Iwamoto Chem. Commun. 1998 1789
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5. Tandem radical translocation and homolytic aromatic substitution: a convenient and efficient route to oxindolesAthelstan L. J. Beckwith,John M. D. Storey J. Chem. Soc. Chem. Commun. 1995 977
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