255062-86-3

Basic information

• Product Name: 2-octyloxybenzoic acid hydrazide
• Synonyms: 2-octyloxybenzoic acid hydrazide
• CAS NO: 255062-86-3
• Molecular Weight: 264.368
• Mol File: 255062-86-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-octyloxybenzoic acid hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-octyloxybenzoic acid hydrazide(255062-86-3)
• EPA Substance Registry System: 2-octyloxybenzoic acid hydrazide(255062-86-3)

Safety Data

• Hazardous Substances Data: 255062-86-3(Hazardous Substances Data)

Upstream product

• 255062-85-2 2-octyloxybenzoic acid methyl ester 

Downstream Products

• 1396804-74-2 C₃₃H₅₀N₆O₆ 
• 1403580-48-2 C₃₈H₅₂N₆O₆ 
• 1235559-15-5 C₁₆H₂₂N₂O₃ 
• 1235559-11-1 C₂₂H₂₉N₃O₃ 
• 1186586-72-0 C₂₂H₃₇N₃O₃ 
• 1186586-75-3 C₂₅H₃₉N₃O₅ 
• 1206874-19-2 C₇₈H₁₀₂N₈O₁₄ 
• 1206874-17-0 C₄₂H₅₈N₄O₇ 
• 787629-33-8 C₅₇H₇₈N₈O₁₂ 
• 787629-32-7 2-methoxy-3-{N'-[5-(N'-{2-methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoyl]-hydrazinocarbonyl}-benzoic acid methyl ester 
• 787629-28-1 5-(N'-{2-Methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoic acid hydrazide 
• 787629-31-6 5-(N'-{2-methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoyl}-hydrazinocarbonyl)-2,4-bis-octyloxy-benzoic acid methyl ester 
• 787629-30-5 2-Methoxy-3-[N'-(2-octyloxy-benzoyl)-hydrazinocarbonyl]-benzoic acid hydrazide 
• 942996-60-3 C₄₅H₆₈N₆O₁₁ 

Relevant articles and documents

Hydrogen bonded oligohydrazide foldamers and their recognition for saccharides

This paper describes the synthesis and characterization of the first series of hydrogen bonding-driven hydrazide foldamers and their recognition for alkyl saccharides in chloroform. Oligomers 1, 2-4, 5, 6, and 7, which contain one, two, four, six, or twel

Hydrazide-Based Quadruply Hydrogen-Bonded Heterodimers. Structure, Assembling Selectivity, and Supramolecular Substitution

This paper describes the synthesis, self-assembly, and characterization of a new class of highly stable hydrazide-based quadruply hydrogen-bonded heterodimers. All of the hydrazide-derived heterodimers possess the complementary ADDA-DAAD hydrogen-bonding sequences. Hydrazide derivatives 1, which has two intramolecular S(6) RO...H-N hydrogen bonds, and 2 complex to afford two fastly exchanging isomeric heterodimers 1·2 and 1·2′ in chloroform, as a result of two different conformational arrangements of 2. An average binding constant Kassoc of 4.7 × 104 M-1 was determined for heterodimer 1·2 and 1·2′ by 1H NMR titration of 1 with changing 2 in chloroform-d. In contrast, 1 binds 11 and 12, both of which are introduced with two intramolecular S(6) hydrogen bonds, to exclusively afford heterodimers 1·11 and 1·12, with Kassoc values of 1.8 × 104 and 5.0 × 102 M-1, respectively. Fluorine-containing 19, which has a hydrazide skeleton identical to that of 1 but two intramolecular S(6) F...H-N hydrogen bonds, can also complex with 2, 11, and 12, to afford heterodimers 19·2, 19·2′, 19·11, and 19·12, with Kassoc values of of 1.2 × 104 (average value for 19·2 and 19·2′), 5.4 × 103, and 1.9 × 102 M-1, respectively. The structures of the new heterodimers have been proven with NOESY, IR, and VPO (for some of the heterodimers) experiments. Moreover, 1 and 19 can also strongly bind 2,7-dilauroylamido-1,8-naphthyridine 23 to afford dimers 1·23 and 19·23 with Kassoc values of 6.0 × 105 and 1.4 × 105 M-1, respectively. Adding 1 to the 1:1 solution of 23 and 1-octyl-3-(4-oxo-3,4-dihydro-pyrido[2,3-d]pyrimidin-2-yl)urea 24 or 1-octyl-3-(4-oxo-1,4-dihydropyrimidin-2-yl)urea 25, which had been developed initially by Zimmerman and Meijer, respectively, induces dimers 23·24 and 23·25 to dissociate, leading to the formation of dimers 1·23 and 24·24 or 25·25, respectively. The new hydrazide-based hydrogen-bonding modules described are useful building blocks for self-assembly and open a new avenue to recognition between discrete supramolecular species.