1185753-91-6

Basic information

• Product Name: dimethyl 5-(isobutyloxy)isophthalate
• Synonyms: dimethyl 5-(isobutyloxy)isophthalate
• CAS NO: 1185753-91-6
• Molecular Weight: 266.294
• Mol File: 1185753-91-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: dimethyl 5-(isobutyloxy)isophthalate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 5-(isobutyloxy)isophthalate(1185753-91-6)
• EPA Substance Registry System: dimethyl 5-(isobutyloxy)isophthalate(1185753-91-6)

Safety Data

• Hazardous Substances Data: 1185753-91-6(Hazardous Substances Data)

Upstream product

• 78-77-3 Isobutyl bromide 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 78-83-1 2-methyl-propan-1-ol 
• 618-83-7 5-Hydroxyisophthalic acid 

Downstream Products

• 1282520-84-6 3-isobutoxy-5-(methoxycarbonyl)benzoic acid 
• 1185753-93-8 5-(isobutyloxy)isophthalic acid 
• 1584144-28-4 dimethyl 5,5'-[2,2'-(4,6-diisobutoxyisophthaloyl)bis(hydrazinylcarbonyl)]bis(3-isobutoxybenzoate) 
• 1584144-31-9 5,5'-[2,2'-(4,6-diisobutoxyisophthaloyl)bis(hydrazinylcarbonyl)]bis-(3-isobutoxybenzoic acid) 
• 1282521-37-2 3-[(phosphonic acid diethyl ester)-methyl]-5-isobutoxy-N-(thiazol-2-yl)-benzamide 
• 1282520-83-5 3-(triphenylphosphonium bromide-methyl)-5-isobutoxy-N-(thiazol-2-yl)benzamide 
• 1282520-85-7 5-isobutoxy-N-(thiazol-2-yl)-isophthalic acid methyl ester 
• 1282520-87-9 3-bromomethyl-5-isobutoxy-N-(thiazol-2-yl)-benzamide 
• 1282520-86-8 3-hydroxymethyl-5-isobutoxy-N-(thiazol-2-yl)-benzamide 
• 1282520-01-7 3-[trans-2-(2-fluorophenyl)vinyl]-5-isobutoxy-N-(thiazol-2-yl)-benzamide 
• 1282519-27-0 3-[trans-2-(3,4-dimethoxyphenyl)vinyl]-5-isobutoxy-N-(thiazol-2-yl)-benzamide 

Relevant articles and documents

Synergistic recognition of halide anions and saccharides by oligohydrazide foldamers

We synthesized and characterized a new kind of hydrazide oligomer that contains two different types of binding moieties for halide anions and saccharides. The addition of either halide anions or saccharides can induce the oligomers to adopt folded conformations. More interestingly, the oligomers are able to complex both chloride anions and saccharides in the cavity at the same time, implying a synergistic molecular recognition. Benzoylbenzohydrazide oligomers containing two different types of binding moieties could be induced to adopt folded conformations by halide anions and saccharides. Moreover, the oligomers could synergistically host these two different kinds of guests in the cavity. Copyright

Two novel quadruple hydrogen-bonding motifs: the formation of supramolecular polymers, vesicles, and organogels

Two new hydrazide-based quadruple hydrogen-bonding motifs are described. Dipodals based on these two motifs are revealed to form supramolecular polymers, which can further aggregate to form vesicles and/or organogels in hydrocarbons. The quadruple hydroge

Organic nanotubes assembled from isophthalamides and their application as templates to fabricate Pt nanotubes

A new class of organic nanotubes have been assembled from simple isophthalamide derivatives and their surface can be conveniently coated with Pt, which form new Pt nanotubes after the inside organic materials are removed with hot methanol.