16308-65-9

Basic information

• Product Name: 5-TERT-BUTYL METHYLISOPHTHALATE
• Synonyms: 5-TERT-BUTYLBENZENE-1,3-BIS-METHYL CARBOXYLATE;5-TERT-BUTYL METHYLISOPHTHALATE;METHYL 5-TERT-BUTYL-ISOPHTHALATE DIESTER;5-Tetr-butyl methylisophthalate;DIMETHYL 5-TERT-BUTYLISOPHTHALATE
• CAS NO: 16308-65-9
• Molecular Formula: C₁₄H₁₈O₄
• Molecular Weight: 250.29
• Mol File: 16308-65-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 334.6°C at 760 mmHg
• Flash Point: 160.2°C
• Appearance: /
• Density: 1.079g/cm³
• Vapor Pressure: 0.000126mmHg at 25°C
• Refractive Index: 1.499
• CAS DataBase Reference: 5-TERT-BUTYL METHYLISOPHTHALATE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-TERT-BUTYL METHYLISOPHTHALATE(16308-65-9)
• EPA Substance Registry System: 5-TERT-BUTYL METHYLISOPHTHALATE(16308-65-9)

Safety Data

• Hazardous Substances Data: 16308-65-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H18O4/c1-14(2,3)11-7-9(12(15)17-4)6-10(8-11)13(16)18-5/h6-8H,1-5H3

Upstream product

• 186581-53-3 diazomethane 
• 2359-09-3 5-t-butylisophthalic acid 
• 253185-03-4 tert-butylbenzene 
• 124-38-9 carbon dioxide 
• 67-56-1 methanol 
• 593-71-5 Chloroiodomethane 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 922-67-8 propynoic acid methyl ester 
• 98-19-1 5-tert-Butyl-m-xylene 

Downstream Products

• 377731-29-8 3-(tert-butyl)-5-(methoxycarbonyl)benzoic acid 
• 1333204-25-3 C₄₀H₃₈N₄ 
• 22157-91-1 1,3-bis(hydroxymethyl)-5-tert-butylbenzene 
• 180740-69-6 5-tert-butylbenzene-1,3-dicarbaldehyde 
• 75894-05-2 1-bis(1-hydroxy-1-methylethyl)-5-(1,1-dimethylethyl)benzene 

Relevant articles and documents

SYNTHETIC METHODS PERTAINING TO TERT-BUTYL-BENZENE-BASED COMPOUNDS

According to some aspects, the present disclosure pertains to methods of forming dimethyl 5-tert-butylisophthalate which comprise comprising converting 5-tert-butylisophthalic acid into dimethyl 5-tert-butylisophthalate in synthesis procedures that compri

BISAMIDE CYTOKINE INHIBITORS

The present invention provides low molecular weight compounds useful as cytokine inhibitors, and compositions thereof. In particular, compounds of the invention are bisamides and are useful as anti-inflammatory agents. In one aspect the compounds have the

Dimetalation: The acidity of monometalated arenes towards superbasic reagents

Twofold hydrogen/metal interconversions ("dimetalations") can be accomplished with "spiny" arenes (tert-butylbenzene, 1,4-di-tert-butylbenzene, 1,1,3,3-tetramethylindane and congeners) and N,N-crowded anilines (2,2,6,6-tetramethyl-1-phenylpiperidine and N