| 词条 | 1,3-Diisopropylbenzene |
| 释义 |
| ImageFile = 1,3-Diisopropylbenzene.svg | ImageSize = 112 px | ImageAlt = | IUPACName = | OtherNames = m-Diisopropylbenzene |Section1={{Chembox Identifiers | CASNo = 99-62-7 | PubChem = 7450 | ChemSpiderID = 7170 | UNII = 482VXW192E | EC_number = 202-773-1 | ChEMBL = 31352 | SMILES = CC(C)C1=CC(=CC=C1)C(C)C | StdInChI=1S/C12H18/c1-9(2)11-6-5-7-12(8-11)10(3)4/h5-10H,1-4H3 | StdInChIKey = UNEATYXSUBPPKP-UHFFFAOYSA-N }} |Section2={{Chembox Properties | C=12|H=18 | Appearance = Colorless liquid | Density = 0.8559 | MeltingPtC = −63 | BoilingPtC = 203 | Solubility = 0.0425 g/l }} |Section3={{Chembox Hazards | GHSPictograms = {{GHS07}}{{GHS08}}{{GHS09}} | GHSSignalWord = Warning | HPhrases = {{H-phrases|335|336|361|400|410}} | PPhrases = {{P-phrases|201|202|261|271|273|281|304+340|308+313|312|391|403+233|405|501}} | MainHazards = | FlashPt = | AutoignitionPtF = 840 }} }}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] References1. ^{{Ullmanns|title=Resorcinol|authors=K. W. Schmiedel, D. Decker|doi=10.1002/14356007.a23_111.pub2|year=2012}} {{DEFAULTSORT:Diisopropylbenzene, 1,3-}} 2 : Alkylbenzenes|Isopropyl compounds |
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