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65232-41-9

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65232-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65232-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65232-41:
(7*6)+(6*5)+(5*2)+(4*3)+(3*2)+(2*4)+(1*1)=109
109 % 10 = 9
So 65232-41-9 is a valid CAS Registry Number.

65232-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenyl-(2,4,6-trimethylphenyl)-ketimin

1.2 Other means of identification

Product number -
Other names 2,4,6-Trimethylbenzophenon-imin

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:65232-41-9 SDS

65232-41-9Relevant articles and documents

Study of the reactivity of organonickel sigma-complexes towards nitriles

Gafurov,Sakhapov,Babaev,Dobrynin,Kurmaz,Metlushka,Rizvanov, I. Kh.,Shaikhutdinova,Sinyashin,Yakhvarov

, p. 254 - 259 (2017/07/11)

The reactivity of organonickel sigma-complexes of type [NiBr(Ar)(bpy)], where Ar = 2,6-dimethylphenyl (Xyl), 2,4,6-trimethylphenyl (Mes), 2,4,6-triisopropylphenyl (Tipp), 2,4,6-tricyclohexylphenyl (Tchp), bpy = 2,2′-bipyridine, towards nitriles (acetonitr

Synthesis of Aryl Ketones by the Pd-Catalyzed C-H Activation of Arenes and Intermolecular Carbopalladation of Nitriles

Zhou, Chengxiang,Larock, Richard C.

, p. 2302 - 2303 (2007/10/03)

The palladium-catalyzed reaction of simple arenes and nitriles provides good to excellent yields of aryl ketones or the corresponding hindered imines. The addition of a small amount of DMSO increases the yields dramatically. Both intermolecular and intramolecular examples of this process are successful. This novel chemistry is believed to involve palladium-catalyzed C?H activation, followed by carbopalladation of the nitrile. Copyright

Flash Vacuum Pyrolysis of 2-Methylbenzophenones and 2-Methyldiphenyl Ketimines

Gu, Taiyin Yang,Weber, William P.

, p. 2541 - 2544 (2007/10/02)

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