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(R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide is a complex organic compound with a unique molecular structure. It is characterized by its chiral centers, which give it specific stereochemistry and potential biological activity. (R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide is derived from a series of chemical reactions and modifications, resulting in a molecule with distinct functional groups and properties.

913358-93-7

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913358-93-7 Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide is used as a pharmaceutical agent for the treatment of various disorders. Its unique structure and functional groups allow it to interact with specific biological targets, modulating their activity and providing therapeutic benefits.
Used in Drug Development:
In the field of drug development, (R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide serves as a potential lead molecule for the discovery of new drugs. Its specific interactions with biological targets can be further optimized to improve its efficacy, selectivity, and safety profile, leading to the development of novel therapeutic agents.
Used in Research Applications:
(R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide is also used in research settings to study the mechanisms of action and potential applications of similar compounds. Its unique properties and interactions with biological systems can provide valuable insights into the development of new therapeutic strategies and drug candidates.
Used in Insomnia Treatment:
As an orally active orexin antagonist (OX1 and OX2 dual receptor antagonist), (R)-2-((R)-6,7-Dimethoxy-1-(4-(trifluoromethyl)phenethyl)-3,4-dihydroisoquinolin-2(1H)-yl)-N-methyl-2-phenylacetamide is used in the treatment of insomnia. It works by blocking the orexin receptors, which play a crucial role in regulating wakefulness, thus promoting sleep and improving sleep quality.

Check Digit Verification of cas no

The CAS Registry Mumber 913358-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,3,5 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 913358-93:
(8*9)+(7*1)+(6*3)+(5*3)+(4*5)+(3*8)+(2*9)+(1*3)=177
177 % 10 = 7
So 913358-93-7 is a valid CAS Registry Number.

913358-93-7SDS

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 Almorexant hydrochloride

1.2 Other means of identification

Product number -
Other names Almorexant 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:913358-93-7 SDS

913358-93-7Downstream Products

913358-93-7Relevant academic research and scientific papers

CRYSTALLINE AND AMORPHOUS FORMS OF ALMOREXANT AND A METHOD OF THEIR PREPARATION

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Page/Page column 5-6, (2011/06/23)

The invention relates to crystalline and amorphous forms of (2R)-2-{(1S)-6,7-dimethoxy-1-[2-(4-trifluoromethyl-phenyl)-ethyl] -3,4-dihydro- 1H-isoquinolin-2-yl} -N-methyl-2-phenyl- acetamide hydrochloride (I) (almorexant) and a method of their preparation

PROCESS FOR THE PREPARATION OF AN ENANTIOMERICALLY PURE TRISUBSTITUTED 1,2,3,4-TETRAHYDROISOQUINOLINE DERIVATIVE

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Page/Page column 20, (2011/02/24)

The present invention relates to a process for the preparation of the compound of formula 7, which process comprises: the asymmetric transfer hydrogenation of the compound of formula 4 * HX: wherein HX is as decribed in the description; in the presence of

TRISUBSTITUTED 3,4-DIHYDRO-1H-ISOQUINOLIN COMPOUND, PROCESS FOR ITS PREPARATION, AND ITS USE

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Page/Page column 13-14, (2010/02/17)

The present invention relates to the compound of formula 7*acetate (see below), a process for its preparation, and its use

PROCESS FOR THE PREPARATION OF AN ENANTIOMERIC TRISUBSTITUTED 3,4-DIHYDRO-ISOQUINOLINE DERIVATIVE

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Page/Page column 7; 14, (2010/12/29)

The present invention relates to a process for the preparation of the compound of formula (7) which process comprises the hydrogenation of the compound of formula (4) using bis[chloro-1,5-cyclooctadiene-iridium], (S)-i-dicyclohexylphosphino-2-[(S)-α-(dime

PROCESS FOR THE PREPARATION OF AN ENANTIOMERIC TRISUBSTITUTED 3,4-DIHYDRO-ISOQUINOLINE DERIVATIVE

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Page/Page column 29, (2009/08/14)

The present invention relates to a process for the preparation of the compound of formula (7) which process comprises the hydrogenation of the compound of formula (4) using bis[chloro-1,5-cyclooctadiene-iridium], (S)-i -dicyclohexylphosphino- 2-[(S)-α-(di

TRISUBSTITUTED 3,4-DIHYDRO-1H-ISOQUINOLIN COMPOUND, PROCESS FOR ITS PREPARATION, AND ITS USE

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Page/Page column 29, (2009/08/14)

The present invention relates to the compound of formula (7*)acetate (see below), a process for its preparation, and its use.

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