1,3-Diisopropylbenzene

1,3-Diisopropylbenzene
Names
	Other names m-Diisopropylbenzene
Identifiers
CAS Number	99-62-7;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL31352;
ChemSpider	7170;
ECHA InfoCard	100.002.521
EC Number	202-773-1;
PubChem CID	7450;
UNII	482VXW192E;
CompTox Dashboard (EPA)	DTXSID8026640 ;
	InChI InChI=1S/C12H18/c1-9(2)11-6-5-7-12(8-11)10(3)4/h5-10H,1-4H3 Key: UNEATYXSUBPPKP-UHFFFAOYSA-N;
	SMILES CC(C)C1=CC(=CC=C1)C(C)C;
Properties
Chemical formula	C12H18
Molar mass	162.276 g·mol−1
Appearance	Colorless liquid
Density	0.8559
Melting point	−63 °C (−81 °F; 210 K)
Boiling point	203 °C (397 °F; 476 K)
Solubility in water	0.0425 g/l
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H335, H336, H361, H400, H410
GHS precautionary statements	P201, P202, P261, P271, P273, P281, P304+340, P308+313, P312, P391, P403+233, P405, P501
Autoignition; temperature	449 °C; 840 °F; 722 K
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

1,3-Diisopropylbenzene is the aromatic hydrocarbon with the formula C₆H₄(CHMe₂)₂ (Me = CH₃). It is one of three isomeric diisopropylbenzenes. This colorless liquid is prepared by thermal isomerization of 1,4-diisopropylbenzene. It is the principal industrial precursor to resorcinol via the Hock rearrangement.[1]

References

K. W. Schmiedel; D. Decker (2012). "Resorcinol". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a23_111.pub2.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] K. W. Schmiedel; D. Decker (2012). "Resorcinol". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a23_111.pub2.