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1-Piperidinecarboxylic acid, 4-[2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]ethyl]-4-hydroxy-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

792239-65-7

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792239-65-7 Usage

Molecular weight

353.52 g/mol

Appearance

Colorless to pale yellow liquid

Melting point

Not applicable (stable liquid)

Boiling point

Not applicable (decomposes before boiling)

Solubility

Insoluble in water, soluble in organic solvents such as ethanol, diethyl ether, and chloroform

Reactivity

Reacts with carboxylic acids and alcohols, can be used to convert carboxylic acids into acyl chlorides

Uses

As a reagent in chemical synthesis, in the production of pharmaceuticals and agrochemicals

Hazard class

Potentially hazardous compound

Regulation

Strictly controlled and regulated due to potential hazards and use in the production of chemical weapons

Physical state

Liquid at room temperature

Purity

Typically used as a pure compound in chemical reactions

Storage

Should be stored in a cool, dry, and well-ventilated area, away from sources of ignition or heat

Check Digit Verification of cas no

The CAS Registry Mumber 792239-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,2,3 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 792239-65:
(8*7)+(7*9)+(6*2)+(5*2)+(4*3)+(3*9)+(2*6)+(1*5)=197
197 % 10 = 7
So 792239-65-7 is a valid CAS Registry Number.

792239-65-7Relevant academic research and scientific papers

Derivatives of piperidinyl-and piperazinyl-alkyl carbamates, preparation methods thereof and application of same in therapeutics

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Page/Page column 13, (2008/06/13)

Compound corresponding to the general formula (I): in which A=N or CR2; R2═H, F, OH, CN, CF3, C1-6-alkyl, C12-6-alkoxy; n=2 or 3 and m=2 when A=N; n=1, 2 or 3 and m=1 or 2 when A=CR2; B=covalent bond or C1-8-alkylene; R1=optionally substituted heteroaryl; R3═CHR4CONHR5; R4═H or C1-6-alkyl; R5═H, C1-6-alkyl, C3-7-cycloalkyl, C3-7-cycloalkyl-C1-C6-alkylene; in the form of a base, an acid-addition salt, a hydrate or a solvate. Therapeutic uses thereof

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