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4-[{2-nitrophenyl}(4-morpholinyl)methyl]morpholine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67589-22-4

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67589-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67589-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,8 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67589-22:
(7*6)+(6*7)+(5*5)+(4*8)+(3*9)+(2*2)+(1*2)=174
174 % 10 = 4
So 67589-22-4 is a valid CAS Registry Number.

67589-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4'-(2-nitro-phenylmethanediyl)-bis-morpholine

1.2 Other means of identification

Product number -
Other names Dimorpholino-(2-nitro-phenyl)-methan

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:67589-22-4 SDS

67589-22-4Relevant academic research and scientific papers

Novel synthesis of α-acetylstyrylphosphonates

Sakoda,Matsumoto,Seto

, p. 705 - 713 (2007/10/02)

α-Acetylstyrylphosphonates were conveniently synthesized from 2-oxopropylphosphonates and substituted (dimorpholinomethyl)-benzenes (animals). 4-Benzylidenemorpholinium carboxylates, generated from animals by the action of α-halo acids, reacted with the phosphonates to give the products by elimination of the amine. The yields were influenced by the nature of substituents and their position in the phenyl ring and could be improved by adjustment of the acidities of the reacted acids. α-Acetylstyrylphosphonates containing various substituents on every position (at the 2-, 3-, or 4-position) in the phenyl ring were obtained generally in excellent yields using monochloroacetic acid.

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