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41661-55-6

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41661-55-6 Usage

Description

1-(2-furylmethyl)piperidin-4-one, also known as 2-(furan-2-ylmethyl)piperidin-4-one, is a chemical compound with the molecular formula C11H15NO2. It is a crystalline solid that features a furan ring and a piperidine ring, which confer unique properties and reactivity to the molecule.

Uses

Used in Pharmaceutical Synthesis:
1-(2-furylmethyl)piperidin-4-one is used as a key intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and reactivity. It plays a crucial role in the development of new drugs and medicinal compounds.
Used in Organic Chemical Synthesis:
1-(2-furylmethyl)piperidin-4-one is also utilized as a starting material in the synthesis of a range of organic chemicals, contributing to the creation of diverse chemical products and materials.
Used in Flavoring Agents for the Food Industry:
1-(2-furylmethyl)piperidin-4-one serves as a flavoring agent, adding unique taste profiles to food products. Its use in the food industry is governed by strict regulations to ensure safety and quality.
Used in Synthesis of Biologically Active Compounds:
As a starting material, 1-(2-furylmethyl)piperidin-4-one is employed in the synthesis of biologically active compounds, which have potential applications in medicine, agriculture, and other fields.
Safety Note:
While 1-(2-furylmethyl)piperidin-4-one has various applications, it is important to handle it with care due to its potential to cause skin and eye irritation upon contact. Proper safety measures should be taken during its use and manipulation.

Check Digit Verification of cas no

The CAS Registry Mumber 41661-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41661-55:
(7*4)+(6*1)+(5*6)+(4*6)+(3*1)+(2*5)+(1*5)=106
106 % 10 = 6
So 41661-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c12-9-3-5-11(6-4-9)8-10-2-1-7-13-10/h1-2,7H,3-6,8H2

41661-55-6 Well-known Company Product Price

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  • Aldrich

  • (CBR00537)  1-(2-Furylmethyl)piperidin-4-one  AldrichCPR

  • 41661-55-6

  • CBR00537-1G

  • 966.42CNY

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41661-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(furan-2-ylmethyl)piperidin-4-one

1.2 Other means of identification

Product number -
Other names 1-Furan-2-ylmethyl-piperidin-4-one

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:41661-55-6 SDS

41661-55-6Downstream Products

41661-55-6Relevant articles and documents

2, 3, 5, 7-tetra-substituted dihydropyrazolo hyxahydro pyridine derivatives and the preparation method and application

-

, (2017/01/31)

The invention provides 2, 3, 5, 7-tetrasubstituted dihydro-pyrazolo piperidine derivative and a preparation method and application thereof. The derivative is 2, 3-bis(substituted phenyl)-5-subsituted arylmethyl-7-substituted benzylidene dihydro-pyrazolo piperidine derivative, having the following formula (I). The preparation method includes using substituted arylmethyl amine and methyl acrylate as raw materials; subjecting the materials to Michael addition, Dieckmann condensation and hydrolysis-decarboxylation sequentially; allowing for Aldol reaction with substituted benzaldehyde to obtain intermediate N-substituted arylmethyl-3, 5-bis(substituted benzylidene)-4-piperidone; allowing for condensation with substituted phenylhydrazine to obtain a compound according to the formula (I). The derivative is efficient in inhibiting multiplication of various carcinoma cell lines such as leukemia, esophagus cancer, ovarian cancer and breast cancer in human, is well stably metabolic in liver microsomes of human and rat, is free of direct and competitive inhibition on five enzymes of liver microsomes, such as CYP3A4, CYP2D6, CYP2C9, CYP1A2 and CYP2C19, is highly bioavailable, is low in toxicity to normal cells, and is available for the preparation of drugs for the cancers.

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