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Benzenamine, N-(cyclohexylmethylene)-2,6-bis(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869085-71-2

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869085-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869085-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,0,8 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 869085-71:
(8*8)+(7*6)+(6*9)+(5*0)+(4*8)+(3*5)+(2*7)+(1*1)=222
222 % 10 = 2
So 869085-71-2 is a valid CAS Registry Number.

869085-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-N-[2,6-di(propan-2-yl)phenyl]methanimine

1.2 Other means of identification

Product number -
Other names Benzenamine,N-(cyclohexylmethylene)-2,6-bis(1-methylethyl)

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:869085-71-2 SDS

869085-71-2Relevant academic research and scientific papers

Intramolecular "hydroiminiumation" of alkenes: Application to the synthesis of conjugate acids of Cyclic Alkyl Amino Carbenes (CAACs)

Jazzar, Rodolphe,Dewhurst, Rian D.,Bourg, Jean-Baptiste,Donnadieu, Bruno,Canac, Yves,Bertrand, Guy

, p. 2899 - 2902 (2007)

(Chemical Equation Presented) A rival for the hydroamination reaction: The intramolecular "hydroiminiumation" reaction features some distinct advantages over intramolecular hydroamination since the resulting prochiral iminium ions potentially allow the su

Thermal Dehydrogenation and Hydrolysis of BH3NH3Catalyzed by Cyclic (Alkyl)(amino)carbene Iridium Complexes under Mild Conditions

Zhou, Lei,Zhang, Dejin,Hu, Jinling,Wu, Youting,Geng, Jiao,Hu, Xingbang

, p. 2643 - 2650 (2021)

Though ammonia-borane (AB) is recognized as an excellent hydrogen storage material, efficient dehydrogenation of AB still remains a challenge. Herein, we report that cyclic (alkyl)(amino)carbene iridium complexes are highly efficient for both the thermal

Highly Ambiphilic Room Temperature Stable Six-Membered Cyclic (Alkyl)(amino)carbenes

Weinstein, Cory M.,Junor, Glen P.,Tolentino, Daniel R.,Jazzar, Rodolphe,Melaimi, Mohand,Bertrand, Guy

supporting information, p. 9255 - 9260 (2018/07/09)

Cyclic (alkyl)(amino)carbenes with a six-membered backbone were prepared. Compared to their five-membered analogues, they feature increased %Vbur and enhanced donor and acceptor properties, as evidenced by the observed n → π? transition trailin

Stable cyclic (alkyl)(amino)carbenes as rigid or flexible, bulky, electron-rich ligands for transition-metal catalysts: A quaternary carbon atom makes the difference

Lavallo, Vincent,Canac, Yves,Praesang, Carsten,Donnadieu, Bruno,Bertrand, Guy

, p. 5705 - 5709 (2007/10/03)

(Chemical Equation Presented) Like NHCs? Not quite: Cyclic (alkyl)-(amino)carbenes (CAACs) are strong σ-donors and have steric environments that differ dramatically from those of bulky, electron-rich phosphines (A) and cyclic diaminocarbenes (B). These re

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