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Urea, N-(4-chlorophenyl)-N'-2-propenyl-, also known as 4-chlorophenyl-2-propenylurea or 4-chlorocinnamylideneurea, is an organic compound with the chemical formula C10H10ClN2O. It is a derivative of urea, featuring a 4-chlorophenyl group and a 2-propenyl group attached to the nitrogen atoms. Urea, N-(4-chlorophenyl)-N'-2-propenyl- is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other chemical products. Due to its reactivity and potential applications, it is important to handle this chemical with care, as it may have toxic or hazardous properties.

37919-93-0

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37919-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37919-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,1 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37919-93:
(7*3)+(6*7)+(5*9)+(4*1)+(3*9)+(2*9)+(1*3)=160
160 % 10 = 0
So 37919-93-0 is a valid CAS Registry Number.

37919-93-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-3-prop-2-enylurea

1.2 Other means of identification

Product number -
Other names HMS1542I16

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:37919-93-0 SDS

37919-93-0Downstream Products

37919-93-0Relevant academic research and scientific papers

Design, synthesis and in vitro biological evaluation of a novel class of anti-adenovirus agents based on 3-amino-1,2-propanediol

Mazzotta, Sarah,Berastegui-Cabrera, Judith,Vega-Holm, Margarita,García-Lozano, María del Rosario,Carretero-Ledesma, Marta,Aiello, Francesca,Vega-Pérez, José Manuel,Pachón, Jerónimo,Iglesias-Guerra, Fernando,Sánchez-Céspedes, Javier

, (2021/06/30)

Nowadays there is not an effective drug for the treatment of infections caused by human adenovirus (HAdV) which supposes a clinical challenge, especially for paediatric and immunosuppressed patients. Here, we describe the design, synthesis and biological evaluation as anti-adenovirus agents of a new library (57 compounds) of diester, monoester and triazole derivatives based on 3-amino-1,2-propanediol skeleton. Seven compounds (17, 20, 26, 34, 44, 60 and 66) were selected based on their high anti-HAdV activity at low micromolar concentration (IC50 from 2.47 to 5.75 μM) and low cytotoxicity (CC50 from 28.70 to >200 μM). In addition, our mechanistic assays revealed that compounds 20 and 44 might be targeting specifically the HAdV DNA replication process, and compound 66 would be targeting HAdV E1A mRNA transcription. For compounds 17, 20, 34 and 60, the mechanism of action seems to be associated with later steps after HAdV DNA replication.

Enzymatic Oxidative Conversion of Thio to Oxo by Baker's Yeast in Thiocarbamates and Thioureas

Kamal, Ahmed,Rao, Maddamsetty V.,Rao, Adari B.

, p. 655 - 656 (2007/10/02)

The enzymatic conversion of aryl allylthiocarbamates and 1-allyl-3-arylthioureas by baker's yeast to the corresponding carbamates and ureas in good yields is described.

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