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1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-phenylpyrrolidin-1-yl)butan-2-yl)thiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1032509-40-2

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1032509-40-2 Usage

Explanation

The compound's full chemical name describes the structure and arrangement of its atoms.

Explanation

L-796568 is a shorter, more manageable name used to refer to the compound in research and development.

Explanation

The compound is made up of carbon, hydrogen, and other elements, with a complex structure.

Explanation

The phenyl group (a ring of six carbon atoms) has two trifluoromethyl groups (CF3) attached to it, which are important for its properties.

Explanation

The thiourea group (NH2-C(S)-NH-C(S)-NH2) is connected to a chiral center, which means it has a specific arrangement of atoms that cannot be superimposed on its mirror image.

Explanation

The chiral center in the compound leads to the existence of stereoisomers, which are molecules with the same molecular formula but different spatial arrangements of atoms.

Explanation

The compound contains a pyrrolidine ring, a five-membered ring with four carbon atoms and one nitrogen atom.

Explanation

The compound has a ketone group (C=O), which is an important functional group for its properties and reactivity.

Explanation

L-796568 has been found to have potential applications in the pharmaceutical industry, particularly as an antidiabetic agent.

Explanation

Scientists are currently exploring the compound's therapeutic properties and potential for use in treating metabolic disorders, as it is not yet an approved drug.

Type of Compound

Complex organic compound

Phenyl Group

Substituted with two trifluoromethyl groups

Thiourea Functional Group

Attached to a chiral center

Chiral Center

Presence of stereoisomers

Pyrrolidine Ring

Part of the compound's structure

Ketone Group

Present in the compound

Potential Application

Pharmaceutical industry

Current Status

Research and development phase

Check Digit Verification of cas no

The CAS Registry Mumber 1032509-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,5,0 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1032509-40:
(9*1)+(8*0)+(7*3)+(6*2)+(5*5)+(4*0)+(3*9)+(2*4)+(1*0)=102
102 % 10 = 2
So 1032509-40-2 is a valid CAS Registry Number.

1032509-40-2Downstream Products

1032509-40-2Relevant academic research and scientific papers

Enantioselective thiourea-catalyzed additions to oxocarbenium ions

Reisman, Sarah E.,Doyle, Abigail G.,Jacobsen, Eric N.

, p. 7198 - 7199 (2008)

Asymmetric, catalytic reactions of oxocarbenium ions are reported. Simple, chiral urea and thiourea derivatives are shown to catalyze the enantioselective substitution of silyl ketene acetals onto 1-chloroisochromans. A mechanism involving anion binding by the chiral catalyst to generate a reactive oxocarbenium ion is invoked. Catalysts bearing tertiary benzylic amide groups afforded highest enantioselectivities, with the optimal structure being derived from enantioenriched 2-arylpyrrolidine derivatives. Copyright

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