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4-Piperidinamine, 1,2,5-trimethyl-N-phenyl-4-(2-propenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113556-37-9

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113556-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113556-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,5 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113556-37:
(8*1)+(7*1)+(6*3)+(5*5)+(4*5)+(3*6)+(2*3)+(1*7)=109
109 % 10 = 9
So 113556-37-9 is a valid CAS Registry Number.

113556-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-trimethyl-N-phenyl-4-prop-2-enylpiperidin-4-amine

1.2 Other means of identification

Product number -
Other names 1,2,5-trimethyl-4-allyl-4-phenylaminopiperidine

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:113556-37-9 SDS

113556-37-9Downstream Products

113556-37-9Relevant academic research and scientific papers

SYNTHESIS OF 4-ALLYL-4-ARYLAMINOPIPERIDINES AND THEIR TRANSFORMATIONS TO SPIRO

Prostakov, N. S.,Kuznetsov, V. V.,Stashenko, E. E.

, p. 1267 - 1271 (1989)

It was established that the yields of a 4-allyl-4-aryl-aminopiperidines in the reaction of 4-aryliminopiperidines with allylmagnesium bromide increase significantly if the reaction is carried out in the presence of a crown ether.A number of previously unknown spiro were obtained in the cyclization of 4-allyl-4-arylaminopiperidines in the presence of sulfuric acid.

SYNTHESIS OF 4-SUBSTITUTED 1-METHYL(BENZYL)-2,5-DIMETHYL-4-R-AMINOPIPERIDINES

Kuznetsov, V. V.,Gaivoronskaya, L. A.,Romero, R. M.,Stashenko, E. E.,Zakharov, P. I.,Prostatkov, N. S.

, p. 783 - 786 (2007/10/02)

Schiff base derivatives of 1-methyl(benzyl)-2,5-dimethylpiperidin-4-ones with phenyl, α-pyridyl, benzyl, and β-hydroxyethyl substituents attached to the imine nitrogen atom react with organometallic compounds to give analogously substituted piperidine bases with methyl, allyl, phenyl, and benzyl substituents in the the 4-position.Pure individual geometric isomers of these newly synthetised compound have been isolated and their structures determined.

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