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Benzenamine, 4-ethoxy-N-(1-phenylethylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20768-50-7

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20768-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20768-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20768-50:
(7*2)+(6*0)+(5*7)+(4*6)+(3*8)+(2*5)+(1*0)=107
107 % 10 = 7
So 20768-50-7 is a valid CAS Registry Number.

20768-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-ethoxyphenyl)-1-phenylethanimine

1.2 Other means of identification

Product number -
Other names p-ethoxyanil of acetophenone

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:20768-50-7 SDS

20768-50-7Relevant academic research and scientific papers

Highly efficient asymmetric-axle-supported N-O amides in enantioselective hydrosilylation of ketimines with trichlorosilane

Pan, Wei,Deng, Yu,He, Jiang-Bo,Bai, Bing,Zhu, Hua-Jie

, p. 7253 - 7257 (2013)

A novel asymmetric-axle-supported chiral N-O amide was synthesized and used in catalytic enantioselective hydrosilylation of N-aryl ketimines with HSiCl3 at room temperature instead of the typical -20°C. High conversion yield and high enantiose

Synthesis and application of axially chiral biscarbolines with functional N-O and sulfone for 1,2-transfer hydrogenations of ketimines

Xing, Yongfei,Wu, Shijie,Dong, Mengxian,Wang, Jie,Liu, Li,Zhu, Huajie

supporting information, (2019/08/08)

A series of axially chiral biscarboline-based sulfones were synthesized from L-tryptophane and applied for enantioselective 1,2-transfer hydrogenations of ketimines using trichlorosilane. The catalyst 4e, which had a tertiary butyl group, exhibited a good conversion and high enantioselectivities up to 96%ee in the series of reactions.

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