The IUPAC name of the spiro compound | 11 | NOMENCLATURE OF ORGANIC COMPOUNDS | CHEMISTRY | DIN... - YouTube
3S,4S,5R,6S,7R)-1-oxaspiro[2.5]octane-4,5,6,7-tetrol, get quote
![36929-66-5 | 1-Oxaspiro[2.5]octane-2-carbonitrile | C8H11NO](https://www.keyorganics.net/app/uploads/2022/08/PS-10258.png "36929-66-5 | 1-Oxaspiro[2.5]octane-2-carbonitrile | C8H11NO")
36929-66-5 | 1-Oxaspiro[2.5]octane-2-carbonitrile | C8H11NO
The IUPAC name of the spiro compound
The correct IUPAC name of spiro compound is - Sarthaks eConnect | Largest Online Education Community
3R,4S,5S,6S)-4-[(2R,3R)-2-Methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1- oxaspiro[2.5]octane-5,6-diol | C15H24O4 | ChemSpider
![1-Oxaspiro[2.5]octane | C7H12O - PubChem](https://pubchem.ncbi.nlm.nih.gov/image/imgsrv.fcgi?cid=9100&t=l "1-Oxaspiro[2.5]octane | C7H12O - PubChem")
1-Oxaspiro[2.5]octane | C7H12O - PubChem
![4R)-2,3β-Bis(4-nitrophenyl)-2-aza-5-oxaspiro[3.4]octane-1-one | Chemical Substance Information | J-GLOBAL](https://jglobal.jst.go.jp/images/chemical/detail/017/386/J1.738.681F.png "4R)-2,3β-Bis(4-nitrophenyl)-2-aza-5-oxaspiro[3.4]octane-1-one | Chemical Substance Information | J-GLOBAL")
4R)-2,3β-Bis(4-nitrophenyl)-2-aza-5-oxaspiro[3.4]octane-1-one | Chemical Substance Information | J-GLOBAL
![1-oxaspiro[2.5]octane-2-carboxylic acid - 6326-84-7, C8H12O3, density, melting point, boiling point, structural formula, synthesis](https://www.chemsynthesis.com/molimg/1/big/17/17813.gif "1-oxaspiro[2.5]octane-2-carboxylic acid - 6326-84-7, C8H12O3, density, melting point, boiling point, structural formula, synthesis")
1-oxaspiro[2.5]octane-2-carboxylic acid - 6326-84-7, C8H12O3, density, melting point, boiling point, structural formula, synthesis
![5-OXA-2-AZA-SPIRO[3.4]OCTANE HEMIOXALATE 10-467856 | CymitQuimica](https://static.cymitquimica.com/products/10/img/467856.png "5-OXA-2-AZA-SPIRO[3.4]OCTANE HEMIOXALATE 10-467856 | CymitQuimica")
5-OXA-2-AZA-SPIRO[3.4]OCTANE HEMIOXALATE 10-467856 | CymitQuimica
![4,5-DIMETHYL-1-OXASPIRO[2.5]OCTANE_Chemical Cloud Database](http://www.chemcd.com/createImage?smile=CC1CCCC2%28C1C%29CO2&size=big.jpg "4,5-DIMETHYL-1-OXASPIRO[2.5]OCTANE_Chemical Cloud Database")
4,5-DIMETHYL-1-OXASPIRO[2.5]OCTANE_Chemical Cloud Database
![909406-73-1|6-Oxaspiro[2.5]octane-1-carboxylic acid| Ambeed](https://file.ambeed.com/static/upload/proimg/443/909406-73-1.png "909406-73-1|6-Oxaspiro[2.5]octane-1-carboxylic acid| Ambeed")
909406-73-1|6-Oxaspiro[2.5]octane-1-carboxylic acid| Ambeed
![Spiro[2.5]octane, 1,1-dichloro- 15997-13-4 wiki](https://structimg.guidechem.com/5/53/1375612.png "Spiro[2.5]octane, 1,1-dichloro- 15997-13-4 wiki")
Spiro[2.5]octane, 1,1-dichloro- 15997-13-4 wiki
![An Efficient Synthesis of 6‐oxa‐spiro[3.4]octan‐1‐one Derivates Through 3‐diazochroman‐4‐one and Alkene - Xiao - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/4d7c95fc-37d0-48cc-80d0-8091b7571053/adsc201701197-toc-0001-m.jpg "An Efficient Synthesis of 6‐oxa‐spiro[3.4]octan‐1‐one Derivates Through 3‐diazochroman‐4‐one and Alkene - Xiao - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library")
An Efficient Synthesis of 6‐oxa‐spiro[3.4]octan‐1‐one Derivates Through 3‐diazochroman‐4‐one and Alkene - Xiao - 2018 - Advanced Synthesis & Catalysis - Wiley Online Library
1-Oxaspiro[2.5]octane, 5,5-dimethyl-4-(3-methyl-1,3-butadienyl)- | C14H22O | ChemSpider
![1-Oxaspiro[2.5]octane, 5,5-dimethyl-4-(3-methyl-1,3-butadienyl)- | C14H22O - PubChem](https://pubchem.ncbi.nlm.nih.gov/image/imgsrv.fcgi?cid=5362888&t=l "1-Oxaspiro[2.5]octane, 5,5-dimethyl-4-(3-methyl-1,3-butadienyl)- | C14H22O - PubChem")
1-Oxaspiro[2.5]octane, 5,5-dimethyl-4-(3-methyl-1,3-butadienyl)- | C14H22O - PubChem
![1523618-29-2 | 5-oxa-2-aza-spiro[3.4]octane hemioxalate | C14H24N2O6](https://www.keyorganics.net/app/uploads/2022/08/AS-34427.png "1523618-29-2 | 5-oxa-2-aza-spiro[3.4]octane hemioxalate | C14H24N2O6")
1523618-29-2 | 5-oxa-2-aza-spiro[3.4]octane hemioxalate | C14H24N2O6
The IUPAC name of the spiro compound
8-hydroxy-5-oxaspiro[2.5]octane-8-carboxylic acid, get quote
![2S)-2-methyl-1-oxaspiro[2.5]octane | C8H14O - PubChem](https://pubchem.ncbi.nlm.nih.gov/image/imgsrv.fcgi?cid=88574631&t=l "2S)-2-methyl-1-oxaspiro[2.5]octane | C8H14O - PubChem")
2S)-2-methyl-1-oxaspiro[2.5]octane | C8H14O - PubChem
![FO74734 | 36929-66-5 | 1-OXASPIRO[2.5]OCTANE-2-CARBONITRILE](https://www.biosynth.com/storage/ChemAxonStructureImages/FO/74/FO74734_structure.png "FO74734 | 36929-66-5 | 1-OXASPIRO[2.5]OCTANE-2-CARBONITRILE")
FO74734 | 36929-66-5 | 1-OXASPIRO[2.5]OCTANE-2-CARBONITRILE
![2-Oxa-5-azaspiro[3.4]octane oxalate, 96%, Thermo Scientific™ | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-1389264-18-9.jpg-250.jpg "2-Oxa-5-azaspiro[3.4]octane oxalate, 96%, Thermo Scientific™ | Fisher Scientific")
2-Oxa-5-azaspiro[3.4]octane oxalate, 96%, Thermo Scientific™ | Fisher Scientific
1-oxaspiro[2.5]octane-2-carboxylic acid - ChemSink
![Buy Ethyl 1-oxaspiro[2.5]octane-2-carboxylate - 6975-17-3 | Benchchem](https://www.benchchem.com/img/structure/B1295103.png "Buy Ethyl 1-oxaspiro[2.5]octane-2-carboxylate - 6975-17-3 | Benchchem")
Buy Ethyl 1-oxaspiro[2.5]octane-2-carboxylate - 6975-17-3 | Benchchem
1-Oxaspiro[2.5]octane | C7H12O | ChemSpider
![Ethyl 1-oxaspiro[2.5]octane-6-carboxylate 95% | CAS: 171361-65-2 | AChemBlock](http://inter.achemblock.com/media/catalog/10776.png "Ethyl 1-oxaspiro[2.5]octane-6-carboxylate 95% | CAS: 171361-65-2 | AChemBlock")