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Hydrazine, 1-benzoyl-2-(p-fluorobenzoyl)-, is a complex organic compound with the chemical formula C14H12FN2O2. It is a derivative of hydrazine, featuring two benzoyl groups attached to the nitrogen atoms, with one benzoyl group being substituted with a fluorine atom on the para position. Hydrazine, 1-benzoyl-2-(p-fluorobenzoyl)- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the preparation of dyes and pigments. Due to its reactivity and the presence of functional groups, it is often used as an intermediate in organic synthesis. The compound's properties, such as its solubility and stability, can be influenced by the presence of the fluorine atom, which can affect its reactivity and selectivity in chemical reactions.

732-95-6

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732-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 732-95-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 732-95:
(5*7)+(4*3)+(3*2)+(2*9)+(1*5)=76
76 % 10 = 6
So 732-95-6 is a valid CAS Registry Number.

732-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-Benzoyl-4-fluorobenzohydrazide

1.2 Other means of identification

Product number -
Other names 4-fluoro-benzoic acid benzoylhydrazide

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:732-95-6 SDS

732-95-6Relevant academic research and scientific papers

In situ generated cetyltrimethylammonium bisulphate in choline chloride-urea deep eutectic solvent: A novel catalytic system for one pot synthesis of 1,3,4-oxadiazole

More, Priyanka Anant,Gadilohar, Balu Laxman,Shankarling, Ganapati Subray

, p. 1393 - 1398 (2014/08/18)

Cetyltrimethylammonium bisulphate ([CTA]HSO4) catalysed one pot synthesis of 2,5-disubstituted-1,3,4-oxadiazoles from carboxylic acid and acid hydrazide in biodegradable deep eutectic solvent is investigated. [CTA]HSO 4 is generated in situ from cetyltrimethylammonium peroxodisulphate. Cyclization of diacylhydrazide using [CTA]HSO4 gives best alternative to traditional dehydration agents. Its remarkable features include a milder procedure, simplicity in workup and purification, good to excellent yields of products, use of inexpensive, recyclable reagents, and eco-friendly aspects by avoiding toxic catalysts/reagents and solvents. Graphical Abstract: [Figure not available: see fulltext.].

17O NMR studies of substituted 1,3,4-oxadiazoles

Gierczyk, Blazej,Zalas, MacIej,Kazmierczak, Marcin,Grajewski, Jakub,Pankiewicz, Radoslaw,Wyrzykiewicz, Bozena

, p. 648 - 654 (2012/01/06)

Three series of substituted 1,3,4-oxadiazoles were studied by 17O NMR spectroscopy. Chemical shifts values were correlated with empirical Hammett parameters as well as calculated bond lengths and chemical shielding values.

Facile synthesis and stracture of novel 2,5-disubstituted 1,3,4-selenadiazoles

Hua, Guoxiong,Li, Yang,Fuller, Amy L.,Slawin, Alexandra M.Z.,Woollins, J. Derek

experimental part, p. 1612 - 1618 (2009/08/09)

The reaction of hydrazide with carbony] chloride in the presence of sodium carbonates leads to the corresponding 1,2- diacylhydrazines [1a-t, R 1C(O)NHNHC(O)R2, R1 = aryl, R2 = aryl or alkyl] in moderate to excellent yield (57-90%). The latter reacts with 2,4-diphenyl-l,3-diselenadiphosphetane- 2,4-diselenide (Woollins' reagent, WR) in refluxing toluene to give a series of new 2,5-disubstituted 1,3,4-selenadiazoles (2a-t, 51-99% yield). All compounds were characterized spectroscopically and six compounds were characterized crystalloqraphically. Wiley-VCH Verlag GmbH & Co. KGaA.

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