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1-methyl-5-phenylpyrazolidin-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14776-37-5

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14776-37-5 Usage

Derivation

Synthetic compound derived from DMAE (dimethylaminoethanol)

Primary Use

Nootropic or smart drug

Cognitive Benefits

Improves memory, learning, and mental performance

Neuroprotective Effects

Preserves brain function and potentially slows cognitive decline

Potential Use

Treating age-related cognitive decline and neurodegenerative diseases such as Alzheimer's

Research Interest

Cognitive enhancer and neuroprotective agent for improving cognitive function and brain health.

Check Digit Verification of cas no

The CAS Registry Mumber 14776-37-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,7 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14776-37:
(7*1)+(6*4)+(5*7)+(4*7)+(3*6)+(2*3)+(1*7)=125
125 % 10 = 5
So 14776-37-5 is a valid CAS Registry Number.

14776-37-5SDS

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 1-methyl-5-phenylpyrazolidin-3-one

1.2 Other means of identification

Product number -
Other names U-6373

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:14776-37-5 SDS

14776-37-5Relevant academic research and scientific papers

Strategy to Prepare 3-Bromo- and 3-Chloropyrazoles

Fox, Richard J.,Schmidt, Michael A.,Eastgate, Martin D.

, p. 2830 - 2839 (2018/03/09)

A general strategy to prepare substituted 3-bromo- and 3-chloropyrazoles is described. The three-step method involves condensation of crotonates or β-chloro carboxylic acids with hydrazines, followed by halogenation and oxidation. Several condensation and oxidation protocols were developed to enable preparation of a wide variety of 3-halopyrazoles with good to excellent yields and regiocontrol.

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