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ethyl 4-toluidinocarbothioylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52009-44-6

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52009-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52009-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,0 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52009-44:
(7*5)+(6*2)+(5*0)+(4*0)+(3*9)+(2*4)+(1*4)=86
86 % 10 = 6
So 52009-44-6 is a valid CAS Registry Number.

52009-44-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-[(4-methylphenyl)carbamothioyl]carbamate

1.2 Other means of identification

Product number -
Other names ethyl 4-toluidinocarbothioylcarbamate

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:52009-44-6 SDS

52009-44-6Relevant academic research and scientific papers

PYRROLO [2,3-B]PYRIDINE-3-CARBOXAMIDE COMPOSITIONS AND METHODS FOR AMELIORATING HEARING LOSS

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Paragraph 00115, (2021/08/13)

N-(3-Substituted thiazol-2(3H)-ylidene)-1H-pyrrolo[2,3-b]pyridine-3-carboxamides and N-(3-substituted oxazol-2(3H)-ylidene)-1H-pyrrolo[2,3-b]pyridine-3-carboxamides (I) and (II) are disclosed. The compounds activate Yap and inhibit Lats kinases. They are therefore useful for treating hearing loss.

THIOPHENE DERIVATIVES FOR THE TREATMENT OF DISORDERS CAUSED BY IGE

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Page/Page column 208, (2020/01/11)

Thiophene derivatives of formula (I) and a pharmaceutically acceptable salt thereof are provided. These compounds have utility for the treatment or prevention of disorders caused by IgE, such as allergy, type 1 hypersensitivity or familiar sinus inflammation.

Concise synthesis of 2-amino-4(3H)-quinazolinones from simple (hetero)aromatic amines

Zeghida, Walid,Debray, Julien,Chierici, Sabine,Dumy, Pascal,Demeunynck, Martine

, p. 2473 - 2475 (2008/09/18)

(Chemical Equation Presented) A novel and simple method of preparation of 2-alkylaminoquinazolin-4-ones with fused heteroaromatic rings from easily accessible (hetero)aromatic amines is described. The method is very efficient, and the 2-alkylaminoquinazolinone derivatives are obtained in three steps without chromatographic purification. The key step is the ring closure of the N-protected guanidine intermediates by intramolecular Friedel-Craft's type substitution.

Efficient and novel synthesis of N-Aryl-N'-ethoxycarbonylthiourea and arene-bis-ethoxycarbonylthiourea derivatives catalyzed by TMEDA

Wei, Tai-Bao,Lin, Qi,Zhang, You-Ming,Wang, Hai

, p. 2205 - 2213 (2007/10/03)

A series of N-aryl-N'-ethoxycarbonyl thioureas and arene-bis- ethoxycarbonylthiourea derivatives have been synthesized in good to excellent yields under the TMEDA catalyzed conditions at room temperature.

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