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(2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride, with the chemical abstracts service number 64671-30-3, is a synthetic organic compound that plays a significant role in various chemical reactions and processes. It is characterized by the presence of a fluorophenyl group and a 1-methyl-4-piperidinyl group attached to a methanone moiety, with a hydrochloride counterion. (2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds.

64671-30-3

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64671-30-3 Usage

Uses

Used in Organic Synthesis:
(2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable building block for the creation of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride is used as a precursor in the development of new drugs. Its structural features can be incorporated into drug molecules to enhance their pharmacological properties, such as potency, selectivity, and bioavailability. (2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride may contribute to the discovery of novel therapeutic agents for the treatment of various diseases and medical conditions.
Used in Chemical Research:
(2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride is also utilized in chemical research to study the properties and reactivity of fluorophenyl and piperidinyl groups. Researchers can use (2-Fluorophenyl)(1-Methyl-4-piperidinyl)-Methanone Hydrochloride to investigate various reaction mechanisms, develop new synthetic methods, and explore the potential of these functional groups in the design of new molecules with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 64671-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,6,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64671-30:
(7*6)+(6*4)+(5*6)+(4*7)+(3*1)+(2*3)+(1*0)=133
133 % 10 = 3
So 64671-30-3 is a valid CAS Registry Number.

64671-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-Fluorophenyl)(1-methyl-4-piperidinyl)-methanone Hydrochloride

1.2 Other means of identification

Product number -
Other names (2-fluorophenyl)-(1-methylpiperidin-4-yl)methanone,hydrochloride

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:64671-30-3 SDS

64671-30-3Downstream Products

64671-30-3Relevant academic research and scientific papers

Antipsychotic 3-(piperidinyl)- and 3-(pyrrolidinyl)-1H-indazoles

-

, (2008/06/13)

Novel 3-(piperidinyl- and 3-(pyrrolidinyl)-1H-indazoles, intermediates and processes for the preparation thereof, and methods for treating psychoses, treating depression, alleviating pain, treating convulsions and treating hypertension utilizing compounds or compositions thereof are disclosed.

3-(4-Piperidinyl)-1,2-benzisothiazoles

-

, (2008/06/13)

Novel 3-(4-piperidinyl)-1,2-benzisothiazoles, processes for the preparation thereof, and method of treating psychoses and alleviating pain employing compounds or compositions thereof are disclosed.

3-(4-Piperidyl)-1,2-benzisoxales

-

, (2008/06/13)

Novel 3-(4-piperidyl)-1,2-benzisoxazoles, intermediates and processes for the preparation thereof, and methods for alleviating pain utilizing compounds or compositions thereof are disclosed.

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