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S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(diMethylaMino)-3-Methylbutan-2-yl)thiourea is a chemical compound with a molecular formula C18H25F6N3S. It is a thiourea derivative that contains trifluoromethyl and dimethylamino functional groups. S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(di
MethylaMino)-3-Methylbutan-2-yl)thiourea is characterized by its unique structure and properties, making it a valuable tool in the development of new drugs and materials. It is used in organic synthesis and pharmaceutical research as a building block or intermediate for the synthesis of various products. However, it is important to handle S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(di MethylaMino)-3-Methylbutan-2-yl)thiourea with proper safety precautions as it may pose health and environmental hazards if not handled carefully.

1048692-50-7

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1048692-50-7 Usage

Uses

Used in Organic Synthesis:
S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(diMethylaMino)-3-Methylbutan-2-yl)thiourea is used as a building block in organic synthesis for the creation of various chemical products. Its unique structure and functional groups contribute to the formation of new compounds with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(diMethylaMino)-3-Methylbutan-2-yl)thiourea serves as an intermediate in the synthesis of new drugs. Its properties and reactivity make it a promising candidate for the development of innovative therapeutic agents.
Used in Drug Development:
S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(diMethylaMino)-3-Methylbutan-2-yl)thiourea is used in drug development as a key component in the design and synthesis of novel pharmaceuticals. Its unique structure allows for the exploration of new chemical spaces and the discovery of potential drug candidates with improved efficacy and safety profiles.
Used in Material Science:
In the field of material science, S-1-(3,5-bis(trifluoroMethyl)phenyl)-3-(1-(diMethylaMino)-3-Methylbutan-2-yl)thiourea can be utilized as a precursor for the development of new materials with specific properties. Its functional groups and reactivity enable the creation of materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1048692-50-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,6,9 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1048692-50:
(9*1)+(8*0)+(7*4)+(6*8)+(5*6)+(4*9)+(3*2)+(2*5)+(1*0)=167
167 % 10 = 7
So 1048692-50-7 is a valid CAS Registry Number.

1048692-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3,5-bis(trifluoromethyl)phenyl]-3-[(2S)-1-(dimethylamino)-3-methylbutan-2-yl]thiourea

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:1048692-50-7 SDS

1048692-50-7Downstream Products

1048692-50-7Relevant academic research and scientific papers

Novel bifunctional chiral urea and thiourea derivatives as organocatalysts: Enantioselective nitro-Michael reaction of malonates and diketones

Andres, Jose M.,Manzano, Ruben,Pedrosa, Rafae

supporting information; experimental part, p. 5116 - 5119 (2009/05/27)

A modular synthesis of novel bifunctional urea and thiourea organocatalysts derived from cheap, easily accessible natural and non-natural amino acids was reported. The generality of the synthesis was demonstrated in the preparation of catalysts 4a-i in th

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