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1-(GAMMA-HYDROXYPROPYL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51452-52-9

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51452-52-9 Usage

Chemical class

Isoquinolines

Explanation

The compound belongs to the class of isoquinolines, which are a group of organic compounds with a bicyclic structure consisting of a benzene ring fused to a pyridine ring.

Explanation

The compound is a hydrochloride salt of a tetrahydroisoquinoline derivative, which means it has a hydrochloric acid (HCl) molecule attached to it, forming a salt.

Explanation

The isoquinoline ring in the compound has a hydroxypropyl (-CH2CH(OH)CH3) and two dimethoxy (-OCH3) substituents, which are responsible for its specific chemical properties.

Explanation

The compound has the potential to act as a neurotransmitter modulator, which means it can influence the activity of neurotransmitters in the brain, potentially leading to psychotropic effects.

Explanation

The compound is being researched for its potential use in the treatment of central nervous system disorders, which are conditions that affect the brain and spinal cord.

Explanation

The compound may have potential as a medication for substance abuse and addiction, possibly due to its ability to modulate neurotransmitter activity in the brain.

Explanation

The compound may possess analgesic (pain-relieving) and anticonvulsant (seizure-preventing) properties, making it a potentially valuable compound in the field of medicine and pharmacology.

Explanation

The compound has a bicyclic structure, with a benzene ring fused to a pyridine ring, which is characteristic of isoquinoline compounds.

Hydrochloride salt

Tetrahydroisoquinoline derivative

Substituents

Hydroxypropyl and dimethoxy groups

Potential pharmaceutical applications

Neurotransmitter modulator

Research focus

Central nervous system disorders

Potential medication

Substance abuse and addiction

Additional properties

Analgesic and anticonvulsant

Structure

Bicyclic organic compound

Check Digit Verification of cas no

The CAS Registry Mumber 51452-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51452-52:
(7*5)+(6*1)+(5*4)+(4*5)+(3*2)+(2*5)+(1*2)=99
99 % 10 = 9
So 51452-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NO3/c1-17-13-8-10-5-6-15-12(4-3-7-16)11(10)9-14(13)18-2/h8-9,12,15-16H,3-7H2,1-2H3/p+1/t12-/m1/s1

51452-52-9SDS

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 1-(γ-HYDROXYPROPYL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names -

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:51452-52-9 SDS

51452-52-9Upstream product

51452-52-9Relevant academic research and scientific papers

Acid promoted cyclodehydration of amino alcohols with amide acetal

Hwang, Soonho,Park, Heemin,Kwon, Yongseok,Kim, Sanghee

, p. 60017 - 60024 (2015/02/19)

A convenient acid-promoted cyclization protocol for the formation of azaheterocycles from amino alcohols is described. The reaction involves the use of N,N-dimethylacetamide dimethyl acetal (DMADA) as the activating reagent of the hydroxyl group. Using this protocol, pyrrolidines or piperidines with various substituents can be synthesized in good to high yields.

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