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112616-18-9

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112616-18-9 Usage

Class

Amides

Contains

Phenyl and morpholine groups

Commonly used in

Research and pharmaceutical development

Known for

Potential pharmacological properties

Often studied for

Potential use in drug discovery

Versatile compound with potential applications in

Various fields of chemistry and medicine

Check Digit Verification of cas no

The CAS Registry Mumber 112616-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,1 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112616-18:
(8*1)+(7*1)+(6*2)+(5*6)+(4*1)+(3*6)+(2*1)+(1*8)=89
89 % 10 = 9
So 112616-18-9 is a valid CAS Registry Number.

112616-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-morpholin-4-yl-N-phenyl-1H-indene-2-carboxamide

1.2 Other means of identification

Product number -
Other names 1H-Indene-2-carboxamide,3-(4-morpholinyl)-N-phenyl

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:112616-18-9 SDS

112616-18-9Upstream product

112616-18-9Relevant articles and documents

The Reaction of Malononitrile with Some Enamines of 1-Indanone. Synthesis of o-Aminonitriles of Indenopyridine and Indenothiopyran

Bogdanowicz-Szwed, Krystyna,Feret, Hanna,Lipowska, Malgorzata

, p. 623 - 627 (2007/10/02)

The reaction of enamines of 1-oxo-indan-2-carboxylic acid anilides (1) with malononitrile yielded 2-arylcarbamylindenylidene-malononitriles (3), which in alkaline solution underwent cyclization to indenopyridines (4).Enamines of 1-oxo-indan-2-carbothionic acid anilides (2) reacted with malononitrile yielding indenothiopyrans (6), which under influence of alkalis were transformed to indenopyridines (8). - Enamines of β-Ketoacid Anilides, o-Aminonitriles, Indenopyridine, Indenothiopyran

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