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1-<(R)-2-(t-butoxycarbonylamino)-2-phenylethanoyl>piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129157-07-9

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129157-07-9 Usage

Structure

A derivative of piperidine with a t-butoxycarbonyl group at the nitrogen atom and a phenethylamide moiety at the carbon atom.

Stereochemistry

(R) at the chiral center, indicating a specific spatial orientation of substituents.

Type of compound

Heterocyclic amine.

Presence in natural products

Commonly found in natural products and pharmaceuticals.

Usage

Used in organic synthesis as a building block for the preparation of various pharmaceutical compounds.

Applications

Potential applications in medicinal chemistry and drug discovery research.

Check Digit Verification of cas no

The CAS Registry Mumber 129157-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,5 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129157-07:
(8*1)+(7*2)+(6*9)+(5*1)+(4*5)+(3*7)+(2*0)+(1*7)=129
129 % 10 = 9
So 129157-07-9 is a valid CAS Registry Number.

129157-07-9Relevant academic research and scientific papers

A new type of L-Tertiary leucine-derived ligand: Synthesis and application in Cu(II)-catalyzed asymmetric Henry reactions

Cai, Zedong,Lan, Ting,Ma, Pengfei,Zhang, Jingfang,Yang, Qingqing,He, Wei

, (2019)

A new series of Schiff bases derived from amino acids were developed as chiral ligands for Cu(II)-catalyzed asymmetric Henry reactions. The optimum ligand 7d exhibited outstanding catalytic efficiency in the Cu(II)-catalyzed asymmetric Henry additions of four nitroalkanes to different kinds of aldehydes to produce 76 desired adducts in high yields (up to 96%) with excellent enantioselectivities, up to 99% enantiomeric excess (ee).

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