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2,5-Pyrrolidinedione, 3-(4-morpholinyl)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53541-45-0

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53541-45-0 Usage

Type of compound

Derivative of glutamic acid

Main uses

Sedative and hypnotic drug

Notable controversy

Teratogenic effects causing severe birth defects in the late 1950s and early 1960s, leading to its withdrawal from the market and strict regulation

Current uses

Treatment of certain cancers and autoimmune diseases

Active properties

Immunomodulatory and anti-inflammatory

Ongoing research

Potential for treating other conditions such as HIV/AIDS and leprosy

Check Digit Verification of cas no

The CAS Registry Mumber 53541-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53541-45:
(7*5)+(6*3)+(5*5)+(4*4)+(3*1)+(2*4)+(1*5)=110
110 % 10 = 0
So 53541-45-0 is a valid CAS Registry Number.

53541-45-0SDS

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 3-(morpholin-4-yl)-1-phenylpyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names 3-MORPHOLINO-1-PHENYLPYRROLIDINE-2,5-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:53541-45-0 SDS

53541-45-0Downstream Products

53541-45-0Relevant academic research and scientific papers

The reaction of benzothiazolyl substituted α-phosphorylmethyl sulfoxides with several amines

Morita, Hiroyuki,Tashiro, Shintaro,Takeda, Masahiro,Yamada, Nobuhiko,Sheikh, Md. Chanmiya,Kawaguchi, Hiroyuki

, p. 4496 - 4505 (2008/09/20)

We have examined the reactivities of α-phosphorylmethyl benzothiazolyl sulfoxides in the thermolyses and in the presence of several amines, such as aniline, benzylamine, piperidine, morpholine, and pyrrolidine. Thermolyses of the derivatives in the presen

From furans to anilines: Toward one-pot two-step amination/Diels-Alder sequences

Medimagh, Raouf,Marque, Sylvain,Prim, Damien,Chatti, Saber,Zarrouk, Hedi

, p. 2191 - 2197 (2008/09/18)

(Chemical Equation Presented) Selective metal-free amination and Diels-Alder reactions are described in the furan series, leading to polysubstituted anilines or to stable oxabicyclic adducts in high yield. Interestingly, anilines are conveniently prepared through a novel one-pot, two-step amination/Diels-Alder procedure from commercially available 5-bromo-2-furaldehyde.

New Reactions of Amino-Functionalized 3-Vinyl-1H-indoles and Tetrahydropyridin-4-yl Analogues with Dienophiles

Medion-Simon, Mercedes,Pindur, Ulf

, p. 430 - 437 (2007/10/02)

Reactions of 3--1H-indole (1), the 1,2-dihydro-9H-carbazole 2, as well as the 3-(tetrahydropyridin-4-yl)-1H-indoles 3a and 3b with some carbo- and heterodienophiles are described.The scope and limitations of the synthetic utility

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