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55750-54-4

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55750-54-4 Usage

Type of compound

Synthetic chemical compound

Uses

Anthelmintic agent for treating parasitic worm infections in humans and animals, immunomodulator, potential therapeutic agent for cancer treatment

Mechanism of action

Paralyzes worms, making it easier for the body to eliminate them

Restrictions

Use has been restricted in certain countries due to potential for harmful side effects and association with severe adverse reactions

Ongoing research

Further research is being conducted to explore levamisole's potential medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 55750-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,5 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55750-54:
(7*5)+(6*5)+(5*7)+(4*5)+(3*0)+(2*5)+(1*4)=134
134 % 10 = 4
So 55750-54-4 is a valid CAS Registry Number.

55750-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dioxopyrrol-1-yl)-3-phenylpropanoic acid

1.2 Other means of identification

Product number -
Other names N,N-maleoyl-L-phenylalanine

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:55750-54-4 SDS

55750-54-4Relevant articles and documents

L-phenylalanine substituted maleimide derivative as well as preparation method and application thereof

-

Paragraph 0040; 0046; 0047, (2018/11/22)

The invention discloses an L-phenylalanine substituted maleimide derivative and a preparation method. The preparation method comprises the following steps: synthesizing 1-aryl-3-methyl-4-formyl-5-(1,2,4-triazolyl)pyrazol; performing dehydration reaction o

Synthesis and properties of chiral N,N-maleoyl derivatives and Diels-Alder reactions with cyclopentadiene

Bodtke,Otto, Hans-Hartwig

, p. 803 - 813 (2007/10/03)

Maleyl amino acid derivatives were prepared from maleic anhydride and cyclized by reaction with ZnCl2 and hexamethyldisilazane yielding maleoyl derivatives. These derivatives were used as dienophiles in cycloadditions with cyclopentadiene. The

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