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94-67-7

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94-67-7 Usage

Uses

Different sources of media describe the Uses of 94-67-7 differently. You can refer to the following data:
1. Salicylaldoxime is an organic compound described by the formula C6H4CH=NOH-2-OH and it is the oxime of salicylaldehyde. This crystalline, colorless solid is a chelator and sometimes used in the analysis of samples containing transition metal ions, with which it often forms brightly colored coordination complexes.
2. As a reagent for copper and nickel.
3. Salicylaldoxime reacts with several metal ions to give intensively coloured complexes which are insoluble in water. The structure of the copper(II), nickel(II) and palladium(II) complexes is shown in Fig. 14 (structure I), and that of the manganese(II), iron(II), cobalt(II) and zinc(II) complexes in Fig. 14 (structure II). The copper(Il) and palladium(II) salicylaldoxime complexes are of importance from an analytical point of view. The complexes precipitated from aqueous media are easily filterable and washable and are weighed after drying at 100°C. The precipitates are of stoichiometric composition. The outstanding stabilities of the copper(II) and palladium(II) complexes make the reagent suitable for the selective determination of these metal ions. These two complexes form quantitatively at low pH values where the complexes of other metal ions do not exist. Besides the gravimetric method, salicylaldoxime is also useful in the volumetric, amperometric and nephelometric determinations of copper and palladium. Salicylaldoxime gives a black precipitate with VOs~ in media containing sulfuric acid; this is soluble in chloroform to give an orange solution. The reaction is specific for vanadium which can thus be detected by this method in the presence of almost all other metals. In neutral medium salicylaldoxime reacts with iron(III) to give a red complex which is soluble in water. The reaction is utilized for the detection of micro amounts of iron.

Elements Extraction

Salicylaldoxime is recognized as a selective precipitant for copper, although it forms water-insoluble chelates with a number of elements. Ingvar Dahl invested the extraction of divalent magnesium, manganese, cobalt, nickel, copper, zinc, cadmium, mercury, and lead with solutions of salicylaldoxime in benzene and the effect of the reagent concentration and particularly the pH of the aqueous phase on the extractability was also studied. The solubility of salicylaldoxime in organic solvents has been utilized in the solvent extraction of carious elements.

Check Digit Verification of cas no

The CAS Registry Mumber 94-67-7 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94-67:
(4*9)+(3*4)+(2*6)+(1*7)=67
67 % 10 = 7
So 94-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO2/c9-7-4-2-1-3-6(7)5-8-10/h1-5,9-10H/b8-5-

94-67-7 Well-known Company Product Price

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  • Alfa Aesar

  • (A11080)  Salicylaldoxime, 98%   

  • 94-67-7

  • 25g

  • 187.0CNY

  • Detail
  • Alfa Aesar

  • (A11080)  Salicylaldoxime, 98%   

  • 94-67-7

  • 100g

  • 681.0CNY

  • Detail
  • Alfa Aesar

  • (A11080)  Salicylaldoxime, 98%   

  • 94-67-7

  • 500g

  • 2424.0CNY

  • Detail
  • Aldrich

  • (84172)  Salicylaldoxime  ≥98.0% (NT)

  • 94-67-7

  • 84172-100G

  • 1,291.68CNY

  • Detail

94-67-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Salicylaldoxime

1.2 Other means of identification

Product number -
Other names 2-hydroxybenzaldehyde oxime

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:94-67-7 SDS

94-67-7Relevant articles and documents

Octamolybdate-based hybrids for direct conversion of aldehydes and ketones to oximes

Han, Pei Pei,Li, Jie,Xing, Cui Li,Zhao, Meng,Han, Qiu Xia,Li, Ming Xue

, (2019)

Two inorganic-organic hybrid materials, [Co(L)2]2Na2[β-Mo8O26]·9H2O (1) and [Fe(L)2]2Na2[β-Mo8O26]·9H2O (2) (HL = 2-acetylpyrazine N4-methyl thiosemicarbazone) have been synthesized and characterized by elemental analyses, infrared (IR) spectroscopy, thermal gravimetric analysis (TGA), powder X-ray diffraction (PXRD) and single-crystal X-ray diffraction. The hybrids 1 and 2 were explored in the oximation of aldehydes and ketones with in situ generated hydroxylamine by a one-pot procedure. In the crystal structures of 1 and 2, N-containing thiosemicarbazide ligands, Lewis acid, and oxidation catalyst octamolybdate coexist within a confined space providing a promising synergistic catalytic way. Hybrids 1 and 2 displayed high catalytic activity and selectivity for the oximation of aldehydes and ketones.

Catalytic performance of a square planar nickel complex for electrochemical‐ and photochemical‐driven hydrogen evolution from water

Du, Juan,Wang, Chun-Li,Yang, Hao,Zhan, Shu-Zhong

, (2021)

A square planar nickel complex bearing salicylketoxime (SAO), Ni-SAO has been synthesized and well characterized by ESI-MS and single-crystal X-ray diffraction, etc. Ni-SAO exhibits good activity in both electrocatalytic and photocatalytic hydrogen evolution reaction (HER). Under an overpotential (OP) of 837.6 mV, Ni-SAO can electrocatalyze hydrogen evolution from a neutral aqueous buffer with a turnover frequency (TOF) of 1428 mol of hydrogen per mole of catalyst per hour (mol H2 /mol catalyst/h). Moreover, under blue light (λ = 469 nm), a three-component system containing Ni-SAO as a catalyst, CdS nanorods (CdS NRs) as a photosensitizer, and ascorbic acid (H2A) as a sacrificial electron donor also can afford hydrogen with a turnover number (TON) of 8138 mol H2 per mol of catalyst (mol of cat?1) during 48 h irradiation. The highest apparent quantum yield (AQY) is about 16.5% at 469 nm.

Photophysical properties of a boron analogue of coumarin

Schrage, Briana R.,Takematsu, Kana,Wang, Huayi,Ziegler, Christopher J.

, p. 18855 - 18862 (2021)

In this report, we present a study into the structure and electronic properties of difluoroboronsalicylaldoxime (DFBS), a boron-based structural analog of coumarin. The modification of the heterocyclic ring of coumarin with boron results in a compound with similar structural parameters and molecular orbitals to coumarin. DFT and TDDFT calculations reveal a significant stabilization of the LUMO in DFBS; this is supported by a ~40 nm red shift of the lowest electronic transition in the absorption spectrum. Interestingly, DFBS is emissive, while unmodified coumarin is effectively non-radiative. Comparisons between DFBS, emissive coumarin variants, and unmodified coumarin suggest that the charge transfer character of the transition contributes to the fluorescence. This journal is

Method for preparing 2-hydroxy-benzonitril by adopting micro-flow field technology

-

Paragraph 0022; 0045-0047, (2021/08/14)

The invention discloses a method for preparing 2-hydroxy benzonitrile (o-hydroxy benzonitrile) by adopting a micro-flow field technology, which comprises the following steps: (1) dissolving hydroxylamine hydrochloride in a solvent, adding salicylaldehyde, and fully stirring and uniformly mixing to obtain a reaction solution; and (2) pumping the uniformly mixed reaction liquid into the micro-channel reactor by adopting single-strand feeding, and carrying out one-step reaction to obtain a 2-hydroxy-benzonitrile crude product. Compared with a traditional preparation method of the 2-hydroxy-benzonitrile, the method has the advantages that the use of a dehydrating agent is avoided, the reaction time is short, the conversion rate of the 2-hydroxy-benzonitrile is high, the operation is simple, the safety is high, and the method is suitable for industrial production.

METHODS OF FORMING IMINES, IMINE-RELATED AND IMINE-DERIVED COMPOUNDS USING GREEN SOLVENTS

-

Paragraph 0180-0183, (2021/10/22)

The present disclosure relates to using green solvents to synthesize an array of imines, imine-related and imine-derived compounds in an efficient and eco-friendly matter, satisfying green chemistry requirements. Reaction embodiments are performed using solvents, such as ethyl lactate and dimethyl isosorbide, which are both individually characterized as green. In embodiments, solvents include lactic whey and/or water as co-solvents. In these green solvents, the synthesis process discussed herein can produce up to quantitative yields of product at room temperature in a short duration. Embodiments include a method of forming an imine, imine-related or imine-derived compound product. In embodiments, the methods include mixing an aldehyde reactant with a nucleophilic/nitrogen-containing reactant in a green solvent at a temperature between negative twenty degrees Celsius (?20° C.) and positive fifty degrees Celsius (50° C.); stirring the mixture; and forming an imine, imine-related or imine-derived compound product.

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