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614-28-8

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614-28-8 Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 65, p. 1624, 1987 DOI: 10.1139/v87-272The Journal of Organic Chemistry, 32, p. 1273, 1967 DOI: 10.1021/jo01279a111

Check Digit Verification of cas no

The CAS Registry Mumber 614-28-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 614-28:
(5*6)+(4*1)+(3*4)+(2*2)+(1*8)=58
58 % 10 = 8
So 614-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO2/c16-13(11-7-3-1-4-8-11)15-14(17)12-9-5-2-6-10-12/h1-10H,(H,15,16,17)

614-28-8SDS

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-benzoylbenzamide

1.2 Other means of identification

Product number -
Other names Benzamide, N-benzoyl-

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:614-28-8 SDS

614-28-8Relevant articles and documents

Copper-Catalyzed Oxidative C?H Bond Functionalization of N-Allylbenzamide for Regioselective C?N and C?O Bond Formation

Ranjith, Jala,Krishna, Palakodety Radha

supporting information, p. 1448 - 1451 (2019/04/03)

Copper-catalyzed oxidative couplings of N-allylbenzamides for C?N and C?O bond formations have been developed through C?H bond functionalization. To demonstrate the utility of this approach, it was applied to the synthesis of β-aminoimides and imides. To the best of our knowledge, these are the first examples in which different classes of N-containing compounds have been directly prepared from the readily available N-allylbenzamides using an inexpensive catalyst/oxidant/base (CuSO4/TBHP/Cs2CO3) system.

Symmetric imide compound and synthetic method thereof

-

Paragraph 0030-0033, (2019/08/07)

The invention discloses a symmetric imide compound and a synthetic method thereof. The method comprises the steps of mixing a compound as shown in the general formula (I) and alkali in aprotic solvent, heating for reaction, and then collecting a compound as shown in the general formula (II) from the reaction product. A series of diaryl imide compounds with representative structure can be obtainedby one-step reaction of simple and easily available activated amide, which is taken as raw material.

A carbonylation reaction of carbon monoxide in the method of preparing amide

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Paragraph 0024; 0025; 0026; 0027; 0028-0032; 0129-0130; 0146, (2018/07/30)

The invention belongs to the technical field of synthesis of amides, discloses a process for the carbonylation of carbon monoxide in the method of preparing amide, the method is to cheap and easy to obtain the halogenated aromatic hydrocarbon and organic amine compounds as the substrate of reaction, to carbon monoxide as carbonyl source, under light-struck, halogenated aromatic hydrocarbons are cracked to produce free radical, by free-radical addition process to obtain the amide compound. Compared with the traditional carbonylation reaction, the carbon monoxide pressure is extremely low, can react to the atmospheric pressure. This process does not need to rely on any metal catalyst of the booster, mild reaction conditions, environmental protection, with a shorter synthetic route and high utilization efficiency of the atoms, the reaction system with higher substrate tolerance, green sustainable light source as the driving force, the atom economy is high, application prospect.

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