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19886-92-1

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19886-92-1 Usage

Chemical class

Alkaloid

Parent compound

Tetrahydroisoquinoline

Natural occurrence

Found in various natural products

Functional groups

Ethyl group, methoxy group, and hydroxyl group

Core structure

Tetrahydroisoquinoline

Pharmaceutical potential

Possible use in developing drugs targeting neurological disorders

Biological activities

Potential for therapeutic applications

Research significance

Interesting molecule for medicinal chemistry and drug discovery studies

Check Digit Verification of cas no

The CAS Registry Mumber 19886-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,8 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19886-92:
(7*1)+(6*9)+(5*8)+(4*8)+(3*6)+(2*9)+(1*2)=171
171 % 10 = 1
So 19886-92-1 is a valid CAS Registry Number.

19886-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-6-methoxy-1,2,3,4-tetrahydroisoquinolin-7-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-ethyl-7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline 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:19886-92-1 SDS

19886-92-1Downstream Products

19886-92-1Relevant articles and documents

1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVES HAVING EFFECTS OF PREVENTING AND TREATING DEGENERATIVE AND INFLAMMATORY DISEASES

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Page/Page column 7, (2010/09/05)

Provided are 7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline derivatives and synthesis methods thereof. The compounds significantly inhibit the production of nitrogen monoxide (NO) and superoxide in an activated microglial cell and expressions of TNF-α, IL-1β inducive NO synthase and cyclooxygenase-2 genes. They also prevent NF-kB shift to a nucleus, decrease reactive oxygen species (ROS), inhibit expression of GTP cyclohydrolase I gene and over-production of tetrahydrobiopterin (BH4), and protect dopaminergic neurons from injury due to activated microglial cells. Consequently, the compounds are effective in treating inflammatory and neurodegenerative diseases.

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