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61449-55-6

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61449-55-6 Usage

Description

1-(4-bromophenyl)-3-methylthiourea is a chemical compound that features a thiourea molecule with a methyl group and a bromophenyl group attached to it. Thioureas are recognized for their wide-ranging applications in organic synthesis and medicinal chemistry. The incorporation of a bromophenyl group in this compound suggests its potential utility in organic reactions as a halogenated building block. Additionally, the methyl group introduces steric effects, which can influence the compound's reactivity and biological activity. As a result, 1-(4-bromophenyl)-3-methylthiourea is a versatile compound with potential applications in various scientific domains, attracting the attention of researchers across different fields.

Uses

Used in Organic Synthesis:
1-(4-bromophenyl)-3-methylthiourea is used as a halogenated building block for its potential role in organic reactions. The presence of the bromophenyl group allows for further functionalization and the creation of a diverse array of chemical products.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-bromophenyl)-3-methylthiourea is utilized for its potential to be developed into therapeutic agents. 1-(4-broMophenyl)-3-Methylthiourea's structural features, including the thiourea and bromophenyl groups, may contribute to its interaction with biological targets, making it a promising candidate for drug discovery and development.
Used in Research and Development:
1-(4-bromophenyl)-3-methylthiourea serves as a valuable compound in scientific research and development. Its unique properties and structural characteristics make it an interesting subject for exploring new reactions, understanding biological activities, and potentially uncovering novel applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 61449-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,4 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61449-55:
(7*6)+(6*1)+(5*4)+(4*4)+(3*9)+(2*5)+(1*5)=126
126 % 10 = 6
So 61449-55-6 is a valid CAS Registry Number.

61449-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromophenyl)-3-methylthiourea

1.2 Other means of identification

Product number -
Other names N-methyl-N'-4-bromophenylthiourea

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:61449-55-6 SDS

61449-55-6Relevant articles and documents

Quantitative solid-state reactions of amines with carbonyl compounds and isothiocyanates

Kaupp, Gerd,Schmeyers, Jens,Boy, Juergen

, p. 6899 - 6911 (2007/10/03)

A series of solid-state reactions is reported of gaseous or solid amines with aldehydes to give imines, with solid anhydrides to give diamides (therefrom imides) or amidic carboxylic salts or imides, with solid imides to give diamides, with solid lactones or carbonates to give functionalized carbamic esters, with polycarbonates to give degradative aminolysis, and with solid isothiocyanates to give thioureas. Diamides give imides by solid-state thermolysis or acid catalysis. Various double, two-step, 3-cascade, and sequential reactions are reported in the solid state without melting. The yields are quantitative in 53 reported reaction examples and no workup (except for washings in four cases) is required in the 100% yield reactions. Three initially solid-state reactions but with liquid product were not quantitative. An upscaling to the kg scale shows promise of the technique for large scale applications. Supermicroscopic analyses with AFM elucidate the solid-state mechanism by virtue of far-reaching anisotropic molecular movements in three-step processes. Gas-solid aminolyses of polycarbonates are also studied with AFM. The implications to sustainable chemistry are discussed. (C) 2000 Elsevier Science Ltd.

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