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Tert-Butyl 5-Methyl-2,4-dioxopiperidine-1-carboxylate, commonly referred to as TBOC, is a chemical compound that serves as a derivative of the amino acid proline. It is recognized for its role in organic synthesis and pharmaceutical research, particularly as a protecting group for amines in peptide synthesis. TBOC is valued for its high stability and the ease with which it can be removed under mild conditions, making it an indispensable tool in the creation of peptides and other intricate organic molecules. Furthermore, its versatile and reliable properties position TBOC as a promising candidate in the development of innovative drugs and pharmaceutical compounds.

942425-69-6

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942425-69-6 Usage

Uses

Used in Pharmaceutical Research:
TBOC is utilized as a protecting group for amines in peptide synthesis, ensuring the integrity and functionality of the amine groups during the synthesis process. Its high stability and the ability to be easily removed under mild conditions make it an essential component in the production of peptides and other complex organic molecules.
Used in Organic Synthesis:
In the realm of organic synthesis, TBOC is employed to protect amines, facilitating the synthesis of complex organic molecules by preventing unwanted side reactions. Its reliable properties and the ease of removal contribute to the successful synthesis of a wide range of organic compounds.
Used in Drug Development:
TBOC's potential applications extend to the development of new drugs and pharmaceutical compounds. Its versatility and reliability make it a valuable asset in the design and synthesis of novel therapeutic agents, potentially leading to advancements in medicine and healthcare.

Check Digit Verification of cas no

The CAS Registry Mumber 942425-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,4,2 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 942425-69:
(8*9)+(7*4)+(6*2)+(5*4)+(4*2)+(3*5)+(2*6)+(1*9)=176
176 % 10 = 6
So 942425-69-6 is a valid CAS Registry Number.

942425-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Piperidinecarboxylic acid, 5-methyl-2,4-dioxo-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names tert-Butyl 5-methyl-2,4-dioxopiperidine-1-carboxylate

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:942425-69-6 SDS

942425-69-6Downstream Products

942425-69-6Relevant academic research and scientific papers

A modular synthesis of novel 4-amino-7,8-dihydro-1,6-naphthyridin-5(6H)- ones as PDE4 inhibitors

Ferrer, Manel,Roberts, Richard S.,Sevilla, Sara

, p. 4821 - 4825 (2013/09/02)

A versatile, modular synthetic route to a series of 4-amino-7,8-dihydro-1, 6-naphthyridin-5(6H)-ones has been developed. These compounds represent a novel structural class of potent phosphodiesterase IV (PDE4) inhibitors.

LEUCINE-RICH REPEAT KINASE ENZYME ACTIVITY

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Page/Page column 64, (2012/05/19)

Disclosed are compounds of Formula (I): and the pharmaceutically acceptable salts thereof, wherein "A" is S-; -SO-, -SO2-, -O- or NRac-, wherein Rac is H, or C1-20 alkyl and R1 through R5 are defined

New 7,8-dihydro-1,6-naphthyridin-5(6h)-one-derivatives as PDE4 inhibitors

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Page/Page column 21; 22, (2011/11/07)

New 7,8-dihydro-1,6-naphthyridin-5(6H)-one derivatives derivatives having the chemical structure of formula (I) are disclosed; as well as process for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of the phosphodiesterase IV (PDE4).

N-substituted pyrrolopyridinones active as kinase inhibitors

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Page/Page column 18, (2010/11/27)

Compounds represented by formula (I) wherein A, R1, R2, R3, R4, R5, and R6 are as defined in the specification, pharmaceutical compositions thereof, and methods of use thereof.

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