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Cyclohexanone, 2-(4-nitrobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38968-78-4

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38968-78-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38968-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,6 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38968-78:
(7*3)+(6*8)+(5*9)+(4*6)+(3*8)+(2*7)+(1*8)=184
184 % 10 = 4
So 38968-78-4 is a valid CAS Registry Number.

38968-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4'-nitro)benzoylcyclohexanone

1.2 Other means of identification

Product number -
Other names 2-(4-nitrobenzoyl)cyclohexanone

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:38968-78-4 SDS

38968-78-4Relevant academic research and scientific papers

Regiochemistry of the condensation of 2-aroyl-cyclohexanones and 2-cyanoacetamide: 13C-labeling studies and semiempirical MO calculations

Van Linden, Oscar P. J.,Wijtmans, Maikel,Roumen, Luc,Rotteveel, Lonneke,Leurs, Rob,De Esch, Iwan. J. P.

, p. 7355 - 7363 (2012/11/07)

Hydroxy-aryl-5,6,7,8-tetrahydroisoquinoline-4-carbonitriles represent interesting chemical scaffolds, but synthetic access to these compounds is limited. The reaction of 2-aroyl-cyclohexanones with 2-cyanoacetamide and base in ethanol has been reported to

High-yielding oxidation of β-hydroxyketones to β-diketones using o-Iodoxybenzoic acid

Bartlett, Samuel L.,Beaudry, Christopher M.

experimental part, p. 9852 - 9855 (2012/01/02)

The oxidation of β-hydroxyketones to β-diketones was systematically investigated. o-Iodoxybenzoic acid (IBX) was found to be efficient, operationally easy, and superior to other common oxidants. The reaction is suitable for milligram- to gram-scale oxidations.

HYDROXAMIC ACID DERIVATIVES

-

, (2010/08/08)

The disclosure includes hydroxamic compounds of Formula I: (I) wherein P, Z, and m are defined herein. Also disclosed is a method for treating a neoplastic disease or an immune disease with these compounds.

Synthesis of Isomeric Series of Aryltetrahydrobenzisoxazoles and Arylcyclopentisoxazoles

Fos, Empar,Borras, Liset,Gasull, Maria,Mauleon, David,Carganico Germano

, p. 203 - 208 (2007/10/02)

Four series of potential PAF-antagonists in which the isoxazole nucleus is condensed with a polyhydrogenated five- or six-carbon ring were prepared.The synthesis of the compounds 3-aryl-4,5,6,7-tetrahydrobenzisoxazoles 1, 3-arylcyclopentisoxazole 2,

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