Indenol

Indenol
	Chemical structure of 1-indenol
Identifiers
CAS Number	1-ol: 56631-57-3;
3D model (JSmol)	1-ol: Interactive image;
ChemSpider	1-ol: 280492;
EC Number	1-ol: 260-294-3;
PubChem CID	1-ol: 316919;
CompTox Dashboard (EPA)	1-ol: DTXSID20972073;
	InChI 1-ol: InChI=1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-6,9-10H Key: KWRSKZMCJVFUGU-UHFFFAOYSA-N;
	SMILES 1-ol: C1=CC=C2C(C=CC2=C1)O;
Properties
Chemical formula	C9H8O
Molar mass	132.162 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Indenols are hydroxylated indene. 3-Indenol is an enol forms of 1-indanone, and 2-indenol is an enol form of 2-indanone. Isomerization of 1-indenol can produce 1-indanone.^[1] Indenolol is a derivative of a phenolic indenol.^[2]

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Indenol

References

Related Articles

Identifiers
Chemical structure of 1-indenol
CAS Number	1-ol: 56631-57-3
3D model (JSmol)	1-ol: Interactive image
ChemSpider	1-ol: 280492
EC Number	1-ol: 260-294-3
PubChem CID	1-ol: 316919
CompTox Dashboard (EPA)	1-ol: DTXSID20972073
InChI 1-ol: InChI=1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-6,9-10H Key: KWRSKZMCJVFUGU-UHFFFAOYSA-N
SMILES 1-ol: C1=CC=C2C(C=CC2=C1)O
Properties
Chemical formula	C₉H₈O
Molar mass	132.162 g·mol⁻¹
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references