17580-69-7

Basic information

• Product Name: Benzaldehyde, 2-hydroxy-5-methoxy-, oxime
• Synonyms: 2-Oxy-5-methoxy-benzaldoxim;Benzaldehyde,2-hydroxy-5-methoxy-,oxime;2-hydroxy-5-methoxy-benzaldehyde-oxime;2-Hydroxy-5-methoxy-benzaldehyd-oxim
• CAS NO: 17580-69-7
• Molecular Formula: C8H9NO3
• Molecular Weight: 167.164
• Mol File: 17580-69-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-hydroxy-5-methoxy-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-hydroxy-5-methoxy-, oxime(17580-69-7)
• EPA Substance Registry System: Benzaldehyde, 2-hydroxy-5-methoxy-, oxime(17580-69-7)

Safety Data

• Hazardous Substances Data: 17580-69-7(Hazardous Substances Data)

Upstream product

• 672-13-9 2-hydroxy-5-methoxybenzaldehyde 
• 150-76-5 4-methoxy-phenol 
• 41951-76-2 2-hydroxy-5-methoxybenzyl alcohol 
• 50-00-0 formaldehyd 

Downstream Products

• 1056956-14-9 Acetic acid 2-cyano-4-methoxy-phenyl ester 
• 109972-88-5 5-methoxysalicylamine 
• 39835-06-8 5-methoxybenzo[d]isoxazole 
• 35924-44-8 6-methoxycoumarin-3-carboxylic acid 
• 39900-63-5 2-cyano-4-methoxyphenol 
• 1081777-51-6 C₈H₁₁NO₂*ClH 

Relevant articles and documents

Hydrogen production on a hybrid photocatalytic system composed of ultrathin CdS nanosheets and a molecular nickel complex

The production of clean and renewable hydrogen through water splitting by using solar energy has received much attention due to the increasing global energy demand. We report an economic and artificial photosynthetic system free of noble metals, consisting of ultrathin CdS nanosheets as a photosensitizer and nickelbased complex as a molecular catalyst. Emission quenching and flash photolysis studies reveal that this hybrid system allows for effective electron transfer from the excited CdS nanosheets to the nickel-based complex to generate reduced intermediate species for efficient hydrogen evolution. Notably, the unique morphological and structural features of the ultrathin CdS nanosheets contribute to the highly efficient photocatalytic performance. As a consequence, the resulting system shows exceptional activity and stability for photocatalytic hydrogen evolution in aqueous solution with a turnover number (TON) of about 28 000 versus catalyst and a lifetime of over 90 h under visible light irradiation.

Calculation and experimental measurement of paramagnetic NMR parameters of phenolic oximate Cu(II) complexes

We present a strategy for predicting the unusual 1H and 13C shifts in NMR spectra of paramagnetic bisoximato copper(ii) complexes using DFT. We demonstrate good agreement with experimental measurements, although 1H-13C correlation spectra show that a combined experimental and theoretical approach remains necessary for full assignment.

HCV PROTEASE INHIBITORS

The present invention discloses a compound of general formula (I); A is O, S, CH, NH or NR', when O links with Z3, Z1 is N or CRZ1, Z2 is CRZ2, when Z1 links with O, Z2 is CH, Z3 is C-Ar; Ra, Rb, Rc and Rd independently is H, OH, halogen or -Y1-Rm; A1 is NH or CH2; R1' is alkyl, aryl, cycloalkyl, heterocycloalkyl or heteroaryl; A2 is N, O or linking bond; R1 is hydrogen, or, R1 linking covalently with R3 forms C5-C9 saturated or unsaturated hydrocarbon chain substituted by O or N; R3 is alkyl, cycloalkyl, heterocycloalkyl, alkyl substituted by cycloalky etc; R4 is alkoxy-CO, alkyl-NHCO, (alkyl)2NCO, or formyl substituted by aryl, cycloalkyl, heterocycloalkyl.