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419571-68-9

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419571-68-9 Usage

Description

Tert-butyl 4-(3-oxobutanoyl)piperidine-1-carboxylate is a chemical compound that serves as an essential reagent in the synthesis of various organic molecules, particularly in the formation of (alkylpyrazolyl)piperidines. It is characterized by its unique structure, which allows for specific chemical reactions and applications in the field of organic chemistry.

Uses

Used in Organic Synthesis:
Tert-butyl 4-(3-oxobutanoyl)piperidine-1-carboxylate is used as a reagent for the regioselective synthesis of (alkylpyrazolyl)piperidines. Its unique structure enables the formation of these complex organic molecules, which can be further utilized in various applications, such as pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, tert-butyl 4-(3-oxobutanoyl)piperidine-1-carboxylate is used as a key intermediate in the synthesis of various drug candidates. Its ability to participate in regioselective reactions allows for the creation of novel compounds with potential therapeutic properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, tert-butyl 4-(3-oxobutanoyl)piperidine-1-carboxylate is employed as a reagent for the synthesis of new compounds with potential applications as pesticides, herbicides, or other agricultural chemicals. Its role in the synthesis of these compounds contributes to the development of more effective and environmentally friendly products.

Check Digit Verification of cas no

The CAS Registry Mumber 419571-68-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,9,5,7 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 419571-68:
(8*4)+(7*1)+(6*9)+(5*5)+(4*7)+(3*1)+(2*6)+(1*8)=169
169 % 10 = 9
So 419571-68-9 is a valid CAS Registry Number.

419571-68-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(3-oxobutanoyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Piperidinecarboxylic acid,4-(1,3-dioxobutyl)-,1,1-dimethylethyl ester

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:419571-68-9 SDS

419571-68-9Downstream Products

419571-68-9Relevant articles and documents

Design, synthesis and biological evaluation of 4-(1- (4(sulphanilamide) phenyl)-3-(methyl)-1H-pyrazol-5-yl)dine urea and N-acyl derivatives as a soluble epoxide hydrolase inhibitors

Nimbarte, Vijaykumar D.,Murtuza, Hadianawala,Phaniraj, Sahishna,Shrivastava, Shweta,Naidu,Satheesh Kumar,Atcha, Krishnam Raju

, p. 2178 - 2197 (2014/05/06)

A series of novel sEH inhibitors containing a N-substituted piperidine ring [N-urea (8a-i ) (9a-l) and amide derivatives (6a-l) (7a-l )] with pyrazole (a five-membered polar heterocycle) as a pharmacophore lead for sEH inhibition have been designed, synth

SUBSTITUTED CYCLOHEXYL DERIVATIVES AS NK-3 RECEPTOR ANTAGONISTS

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Page/Page column 30-31, (2010/11/25)

The present invention relates to the compounds of formula (I): wherein A,B, n, X, Y, Z, R1, R2, R3, R4, R5, R6, R7 and R8 are defined herein, and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising them and their use in treating diseases mediated by neurokinin-3 (NK-3) receptors. These compounds can thus be used in methods of treatment to suppress and treat such disorders.

N-(3-(4-substituted-1-piperidinyl)-1-phenylpropyl) substituted sulfonamides as NK-3 receptor antagonists

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Page/Page column 34, (2010/11/30)

The present invention provides a method of treatment of a subject suffering from a disease, such as schizophrenia, for which the administration of an NK-3 antagonist is indicated which comprises administering to that subject a therapeutically effective amount of a compound of formula I: wherein, generally, Q is R1 is benzyl, phenyl, thiophene or imidazolyl optionally substituted with C1-4alkyl or halogen, such as methyl, fluorine or bromine; R2 is hydrogen or C1-4alkyl such as methyl; R3 is phenyl; R4 is hydrogen; R5 is hydrogen or C1-6alkylcarbonyl such as methylcarbonyl; X is —SO2— or —C(O)N(R2)SO2— where R2 is preferably hydrogen; Y is a bond, CH2 or Z1 where Z1 is —N(Rf)— in which Rf is C1-6alkylcarbonyl such as ethylcarbonyl; and R6 is phenyl, pyrazolyl, pyridyl, pyrimidinyl or benzimidazolonyl optionally substituted with one or two groups chosen from C1-6alkyl and benzyl, such as methyl, ethyl and benzyl; or a pharmaceutically acceptable salt thereof.

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