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Ethanone, 1-(2-naphthalenyl)-2-(phenylamino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62244-84-2

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62244-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62244-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62244-84:
(7*6)+(6*2)+(5*2)+(4*4)+(3*4)+(2*8)+(1*4)=112
112 % 10 = 2
So 62244-84-2 is a valid CAS Registry Number.

62244-84-2SDS

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 2-anilino-1-naphthalen-2-ylethanone

1.2 Other means of identification

Product number -
Other names 2-(Anilinoacetyl)-naphthalin

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:62244-84-2 SDS

62244-84-2Relevant academic research and scientific papers

Synthesis of (Z)-nitroalkene derivatives through oxidative dehydrogenation coupling of α-aminocarbonyl compounds with nitromethane by copper catalysis

Zhu, Menghua,Chen, De,Zeng, Sheng,Xing, Chenhu,Deng, Wei,Xiang, Jiannan,Wang, Rui-Jia

supporting information, p. 3214 - 3219 (2018/07/21)

A novel copper-catalyzed cross-dehydrogenative coupling reaction of α-amino carbonyl compounds with nitromethane to synthesis of (Z)-nitroalkene derivatives has been established. (Z)-Nitroalkene derivatives are achieved through the cleavage of sp3 CsbndH bonds and formation of CsbndC double bond, with mild reaction conditions and excellent stereoselectivity.

Kinetics of Reactions of ω-Bromo-2-acetonaphthone with Pyridine and Substituted Anilines in Various Solvents

Ananthakrishnanadar, P.,Varghesedharumaraj, G.,Subramanian, S. V.

, p. 953 - 956 (2007/10/02)

Rate constants for the reactions of ω-bromo-2-acetonaphthone with aniline and pyridine in various protic and aprotic solvents have been determined at three temperatures.The rates of reaction with pyridine in simple alcohols are less than those with aniline.Values of Hammet ρ-constant have been obtained for the reactions with substituted anilines in a few solvents.Multiple correlation of log k40 deg C for the reaction with aniline in various alcohols employing several solvent parameters is highly successful.

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