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4706-74-5

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4706-74-5 Usage

General Description

The chemical 2-(piperidin-1-ylmethyl)-3,4-dihydronaphthalen-1(2H)-one is a compound with a complex molecular structure. It contains a piperidine ring and a dihydronaphthalen-1-one group, and is commonly used in pharmaceutical research. This chemical has potential applications in the development of new drugs targeting various medical conditions. Its unique structure and properties make it a valuable building block for the synthesis of biologically active compounds and potential therapeutic agents. Further research and study of this chemical may lead to the discovery of new pharmaceuticals with important medical implications.

Check Digit Verification of cas no

The CAS Registry Mumber 4706-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4706-74:
(6*4)+(5*7)+(4*0)+(3*6)+(2*7)+(1*4)=95
95 % 10 = 5
So 4706-74-5 is a valid CAS Registry Number.

4706-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(piperidin-1-ylmethyl)-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 2-Piperidinomethyl-1-tetralone

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:4706-74-5 SDS

4706-74-5Downstream Products

4706-74-5Relevant articles and documents

A modified Mannich reaction using 1,3-dioxolane

Sumita,Koumori,Ohno

, p. 1676 - 1678 (2007/10/02)

Mannich reaction of ketones using 1,3-dioxolane instead of formaldehyde, paraformaldehyde, or 1,3,5-trioxane afforded the corresponding Mannich bases in high yields. Under the same conditions the aminomethylation of aromatics did not proceed but the intramolecular aminomethylation, like a Pictet-Spengler type reaction, proceeded smoothly.

Analgesic and tranquilizing activity of 5,8 disubstituted 1 tetralone Mannich bases

Welch,Harbert,Sarges,Stratten,Weissman

, p. 699 - 705 (2007/10/04)

5,8-Disubstituted 1-tetralone Mannich bases represent semirigid variants of classical (i.e., chlorpromazine) neuroleptic agents. 8-Chloro-5-methoxy-2- morpholinomethyl-1-tetralone exhibits neuroleptic potency in the thiothixene range in animal models. Of greater potential interest, however, is the analgesic potency of the 8-chloro-5-methoxy-2-pyrrolidinomethyl analogue which was in the morphine range. This compound did not induce tolerance nor was its activity reversed by naloxone. Structure-activity relationships of the series are discussed.

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