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1H-Isoindole-1,3(2H)-dione, 2-[(3,6-dihydro-4-phenyl-1(2H)-pyridinyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61365-26-2

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61365-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61365-26-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61365-26:
(7*6)+(6*1)+(5*3)+(4*6)+(3*5)+(2*2)+(1*6)=112
112 % 10 = 2
So 61365-26-2 is a valid CAS Registry Number.

61365-26-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-phenyl-1,2,3,6-tetrahydropyridin-1-ylmethyl)phthalimide

1.2 Other means of identification

Product number -
Other names 2-[(3,6-Dihydro-4-phenyl-1(2H)-pyridinyl)methyl]-1H-isoindole-1,3(2H)-dione

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:61365-26-2 SDS

61365-26-2Relevant academic research and scientific papers

Photochemical Cyclisation of Phthalimide Mannich Bases

Coyle, John D.,Newport, Graham L.

, p. 93 - 96 (2007/10/02)

Ultraviolet irradiation of Mannich bases derived from phthalimide, formaldehyde, and a secondary amine leads to cyclised products containing a new imidazolidine ring.The reaction is much less efficient when the secondary amine has an aromatic group adjacent to the nitrogen atom.Exceptionally, the Mannich base derived from 3-pyrroline does not cyclise but undergoes an internal oxidation-reduction reaction to give a substituted pyrrole.

2-[(4-Phenyl-tetrahydropyridinyl)alkyl]-1H-isoindole-1,3(2H)-diones

-

, (2008/06/13)

Compounds having the formula SPC1 Wherein A is a straight or branched chain alkylene group; R1 is hydrogen, halogen, alkyl, alkoxy, alkylthio, nitro, amino, or cyano; and R2 is hydrogen, halogen, alkyl, alkoxy, trifluoromethyl, nitro

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