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935-07-9

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935-07-9 Usage

Description

Acetaldehyde phenylhydrazone is a chemical compound formed by the reaction of acetaldehyde and phenylhydrazine. It is a yellow crystalline solid that is commonly used in the identification and quantification of aldehydes in organic compounds.

Uses

Used in Organic Synthesis:
Acetaldehyde phenylhydrazone is used as a stable complex for aldehydes in organic synthesis for its ability to easily isolate and characterize aldehydes.
Used in Analytical Chemistry:
Acetaldehyde phenylhydrazone is used as a detection and measurement tool for aldehydes, playing a crucial role in the identification and quantification of these compounds.
Used in Pharmaceutical Research:
Acetaldehyde phenylhydrazone is used as a synthetic intermediate for the synthesis of various organic compounds in pharmaceutical research, contributing to the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 935-07-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 935-07:
(5*9)+(4*3)+(3*5)+(2*0)+(1*7)=79
79 % 10 = 9
So 935-07-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2/c1-2-9-10-8-6-4-3-5-7-8/h2-7,10H,1H3/b9-2+

935-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-ethylideneamino]aniline

1.2 Other means of identification

Product number -
Other names 1-ethylidene-2-phenylhydrazine

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:935-07-9 SDS

935-07-9Relevant articles and documents

Shaken, not stirred: a schools test for aldehydes and ketones

Plater, M John

, p. 104 - 107 (2019/11/22)

A schools test for aldehydes and ketones in water at room temperature using test tubes has been developed in this laboratory using either phenylhydrazine hydrochloride or phenylhydrazine hydrochloride with NaOAc . 3H2O. The role of one equivalent of a strong or weak acid which catalyses the reaction is discussed.

Polyaromatic hydrocarbon derivatized azo-oximes of cobalt(iii) for the ligand-redox controlled electrocatalytic oxygen reduction reaction

Dinda, Soumitra,Roy, Syamantak,Patra, Sarat Chandra,Bhandary, Subhrajyoti,Pramanik, Kausikisankar,Ganguly, Sanjib

, p. 3737 - 3747 (2020/03/17)

A pair of ligands HLPyr1a and HLAnc1b (Pyr = pyrene, Anc = anthracene) incorporating π-electron-rich polycyclic aromatic hydrocarbons (PAHs), viz. pyrene and anthracene moieties respectively, in conjunction with electron-poor azo-oxime groups was synthesized. The tris complexes [CoIII(LPyr)3] 2a and [CoIII(LAnc)3] 2b were also prepared and structurally authenticated by X-ray diffraction. They exhibit significant redox and optoelectronic properties, which were analyzed by density functional theory (DFT) and time dependent density functional theory (TD-DFT). Theoretical investigation further revealed that the coordinated ligands act as superior electron reservoirs in comparison to the free ligands and transfer electrons through the PAH moieties. This property was smartly exploited to scrutinize the aptitude of the cobalt(iii) complexes for the electrocatalytic oxygen reduction reaction (ORR). The catalytic process proceeds via a 4-electron transfer pathway to form hydroxide ions in alkaline medium. The role of the PAHs in the complexes 2a and 2b in providing a pool of electrons was further emphasized via substituting them with phenyl groups, as in [CoIII(LPh)3] 2c, when the catalytic ORR activity was significantly diminished. Moreover, the activity was completely lost when the PAHs were replaced by methyl groups, as in [CoIII(LMe)3] 2d.

Oxidized single-walled carbon nanotubes (swcns-cooh) as a new catalyst for the protection of carbonyl groups as hydrazones

Borazjani, Maryam Kiani,Safaei, Hamid Reza,Panahandeh, Majid,Kiani, Ali Reza,Kiani, Masoumeh,Mofarahi, Masoud

, p. 279 - 281 (2013/12/04)

Nano-materials are considered as suitable heterogeneous catalysts for many organic reactions. Herein oxidized carbon nanotube (SWCNTs-COOH) has been reported as a heterogeneous catalyst, for protection of carbonyl groups as hydrazones in EtOH at 80 C. The reactions proceed smoothly with good to excellent yields, and the SWCNTs-COOH used can be recycled.

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