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L-Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is a chemical compound derived from tetrahydroisoquinoline, a tricyclic compound found in various natural products. It is known for its potential pharmacological properties, such as acting as a central nervous system stimulant, and exhibiting anti-inflammatory and analgesic effects. Additionally, it has shown promise in antiparkinsonian and neuroprotective properties, making it a valuable candidate for drug development and neuropharmacology research.

15912-56-8

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15912-56-8 Usage

Uses

Used in Pharmaceutical Research:
L-Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is used as a research compound for its potential pharmacological properties, including its ability to stimulate the central nervous system, and its potential anti-inflammatory and analgesic effects.
Used in Neuropharmacology Research:
In the field of neuropharmacology, L-Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is used as a candidate for further drug development due to its potential antiparkinsonian and neuroprotective properties, which could contribute to the treatment and management of neurological disorders.
Used in Drug Development:
L-Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is utilized in drug development for its potential therapeutic applications, particularly in the areas of central nervous system stimulation, pain management, and neuroprotection, offering new avenues for the treatment of various conditions and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 15912-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,1 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15912-56:
(7*1)+(6*5)+(5*9)+(4*1)+(3*2)+(2*5)+(1*6)=108
108 % 10 = 8
So 15912-56-8 is a valid CAS Registry Number.
InChI:InChI=1S/C12H15NO2.ClH/c1-2-15-12(14)11-7-9-5-3-4-6-10(9)8-13-11;/h3-6,11,13H,2,7-8H2,1H3;1H/t11-;/m0./s1

15912-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate,hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-Ethyl 1,2,3,4-tetrahydroisoquinoline-3-carboxylate HCl

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:15912-56-8 SDS

15912-56-8Relevant academic research and scientific papers

HETEROCYCLES FOR USE AS INHIBITORS OF LEUKOTRIENES

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, (2008/06/13)

The invention concerns a heterocycle of the formula I wherein Q is an optionally substituted 6-membered monocyclic or 10-membered bicyclic heterocyclic moiety containing one or two nitrogen atoms; A is (1-6C)alkylene, (3-6C)alkenylene, (3-6C)alkynylene or cyclo(3-6C)alkylene; X is oxy, thio, sulphinyl, sulphonyl or imino; Ar is phenylene which may optionally bear one or two substituents or Ar is an optionally substituted 6-membered heterocyclene moiety containing up to three nitrogen atoms; R 1 is hydrogen, (1-6C)alkyl, (3-6C)alkenyl, (3-6C)alkynyl, cyano-(1-4C)alkyl or (2-4C)alkanoyl, or optionally substituted benzoyl; and R 2 and R 3 together form a group of the formula --A 2 --X 2 --A 3 -- which, together with the carbon atom to which A 2 and A 3 are attached, defines a ring having 4 to 7 ring atoms, wherein A 2 and A 3, which may be the same or different, each is (1-4C)alkylene and X 2 is oxy, thio, sulphinyl, sulphonyl or imino; or a pharmaceutically-acceptable salt thereof. The compounds of the invention are inhibitors of the enzyme 5-lipoxygenase.

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