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Acetamide, N-acetyl-N-(1,2-diphenylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65693-77-8

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65693-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65693-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,9 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65693-77:
(7*6)+(6*5)+(5*6)+(4*9)+(3*3)+(2*7)+(1*7)=168
168 % 10 = 8
So 65693-77-8 is a valid CAS Registry Number.

65693-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-N-(1,2-diphenylvinyl)acetamide

1.2 Other means of identification

Product number -
Other names -

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:65693-77-8 SDS

65693-77-8Downstream Products

65693-77-8Relevant academic research and scientific papers

BENZOPHENANTHRIDINES. X. INVESTIGATION OF THE RODIONOV-SUVOROV SCHEME. REDUCTIVE ACETYLATION OF THE OXIMES OF 3-ETHOXYCARBONYL-SUBSTITUTED 2-PHENYLTETRAL-1-ONES WITH STANNOUS CHLORIDE IN ACETIC ANHYDRIDE

Maslennikova, L. V.,Sladkov, V. I.,Levina, I. I.,Kurkovskaya, L. N.,Suvorov, N. N.

, p. 2165 - 2170 (2007/10/02)

When treated with anhydrous stannous chloride in acetic anhydride, the oximes of benzyl phenyl ketone and 3-alkoxycarbonyl- and 3,3-dialkoxycarbonyl-2-phenyltetralones give a mixture of enamides and enimides.The direction of the reaction does not depend on the configuration of the oxime.It takes place in a more well-defined manner with the derivatives of 2-phenyltetralones used in the synthesis of benzophenanthridines by the Rodionov-Suvorov method.

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