39630-68-7

Basic information

• Product Name: 5-HYDROXY-ISOPHTHALIC ACID DIETHYL ESTER
• Synonyms: diethyl 5-hydroxyisophthalate
• CAS NO: 39630-68-7
• Molecular Formula: C₁₂H₁₄O₅
• Molecular Weight: 238.24
• Mol File: 39630-68-7.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 382.7°C at 760 mmHg
• Flash Point: 145.3°C
• Appearance: /
• Density: 1.211g/cm³
• Vapor Pressure: 2.11E-06mmHg at 25°C
• Refractive Index: 1.532
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-HYDROXY-ISOPHTHALIC ACID DIETHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 5-HYDROXY-ISOPHTHALIC ACID DIETHYL ESTER(39630-68-7)
• EPA Substance Registry System: 5-HYDROXY-ISOPHTHALIC ACID DIETHYL ESTER(39630-68-7)

Safety Data

• Hazardous Substances Data: 39630-68-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O5/c1-3-16-11(14)8-5-9(7-10(13)6-8)12(15)17-4-2/h5-7,13H,3-4H2,1-2H3

Upstream product

• 23351-91-9 5-bromoisophthalic acid 
• 121-91-5 isophthalic acid 
• 64-17-5 ethanol 
• 22326-31-4 5-sulfoisophthalic acid 
• 618-83-7 5-Hydroxyisophthalic acid 

Downstream Products

• 113585-32-3 C₃₄H₄₆O₁₀ 
• 208511-31-3 N,N-bis[2-(3,5-bis(ethoxycarbonyl)phenoxy)ethyl]-p-toluene sulfonamide 
• 371919-09-4 tetra(ethylene glycol) bis(3,5-diethoxycarbonyl)phenyl ether 
• 153707-56-3 3,5-bis(hydroxymethyl)phenol 
• 918402-87-6 5-tert-butoxycarbonyloxy-isophthalic acid diethyl ester 
• 350671-22-6 N,N'-Bis[2-(6-aminopyridyl)]-5-(4-nitrophenylmethyloxy)isophthaldiamide 
• 350671-23-7 N,N'-Bis[2-(6-butyrylaminopyridyl)]-5-(4-nitrophenylmethyloxy)isophthaldiamide 
• 251912-48-8 [5-(benzyloxy)-1,3-phenylene]dimethanol 
• 251912-33-1 O-benzyl-3,5-bis(phenylthiomethyl)phenol 
• 147566-72-1 1,3-bis((3,5-diethoxycarbonylphenoxy)methyl)benzene 
• 155186-12-2 α,α'-bis<3,5-bis(dicarbethoxy)phenoxy>-o-xylene 

Relevant articles and documents

THE INHIBITION OF GLUTAMATE DEHYDROGENASE BY DERIVATIVES OF ISOPHTHALIC ACID

A range of compounds, structurally related to glutamate, have been tested as inhibitors of pea leaf glutamate dehydrogenase assayed in either direction.Only 5-N-substituted derivatives of aminoisophthalic acid completely inhibited the enzyme when tested at concentrations equal to either those of 2-oxoglutarate or glutamate.A minimum of three carbon atoms attached linearly to the amino group was required for maximum inhibition, inhibition was removed if there was any substitution on the first carbon.The 5-N-substituted derivatives also inhibited yeast (to a greater extent) and bovine liver (to a lesser extent) glutamate dehydrogenases.Key Word Index - Pisum sativum; Leguminoseae; yeast; bovine; glutamate dehydrogenase inhibition; isophthalic acid derivatives.

Nano composite of polynucleotide and gold nano rod, and preparation method and applications thereof

The invention discloses a nano composite of polynucleotide and gold nano rod, and a preparation method and applications thereof. The surface of a nano gold rod is modified by a polynucleotide carrier compound, which is modified by lipoic acid having high

In-situ generation of differential sensors that fingerprint kinases and the cellular response to their expression

Mitogen-activated protein (MAP) kinases are responsible for many cellular functions, and their malfunction manifests itself in several human diseases. Usually, monitoring the phosphorylation states of MAP kinases in vitro requires the preparation and puri