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CAS

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97294-78-5

(R)-1-(3,5-diMethoxyphenyl)ethanamine, a chiral amine belonging to the phenethylamines class, is a substituted phenethylamine with two methoxy functional groups attached to the benzene ring. As a chiral compound, it possesses a stereocenter and exists in two enantiomeric forms, (R)and (S)-. Its potential psychoactive properties and unique chemical structure make it a valuable subject for research in medicinal chemistry, pharmacology, and neuroscience.

97294-78-5

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97294-78-5 Usage

Uses

Used in Medicinal Chemistry:
(R)-1-(3,5-diMethoxyphenyl)ethanamine is used as a research compound for exploring its potential psychoactive properties and understanding its interactions with biological systems. Its unique structure and chirality offer opportunities for the development of novel therapeutic agents.
Used in Pharmacology:
In the field of pharmacology, (R)-1-(3,5-diMethoxyphenyl)ethanamine serves as an experimental compound to study its effects on the central nervous system and its potential as a therapeutic agent for various neurological disorders.
Used in Neuroscience:
(R)-1-(3,5-diMethoxyphenyl)ethanamine is utilized as a research tool in neuroscience to investigate its impact on neurotransmitter systems and its potential role in modulating cognitive and emotional processes.
Note: The specific applications and industries for (R)-1-(3,5-diMethoxyphenyl)ethanamine are not explicitly mentioned in the provided materials. The uses listed above are inferred based on its potential properties and relevance to the mentioned fields.

Check Digit Verification of cas no

The CAS Registry Mumber 97294-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,9 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97294-78:
(7*9)+(6*7)+(5*2)+(4*9)+(3*4)+(2*7)+(1*8)=185
185 % 10 = 5
So 97294-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-7(11)8-4-9(12-2)6-10(5-8)13-3/h4-7H,11H2,1-3H3/t7-/m1/s1

97294-78-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-dimethoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 1-(3,5-Dimethoxyphenyl)ethylamine

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:97294-78-5 SDS

97294-78-5Relevant articles and documents

ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Paragraph 0288; 0291; 0292; 0960; 961; 0962, (2017/06/12)

A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.

SUBSTITUTED ARYLAMINE COMPOUNDS AND THEIR USE AS 5-HT6 MODULATORS

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Page/Page column 73-74, (2008/06/13)

The invention relates to 5-HT6 receptor antagonists. Novel arylamine compounds having the formula: (see formula I) and pharmaceutically acceptable salts and/or esters thereof, wherein - n is 0, 1, 2, 3, or 4; - A, when present is a lower alkyl

Chiral Building Blocks for the Synthesis of Nitrogen-Containing Natural Products, 5. The Enantioselective Synthesis of Optically Active, Benzene Nucleus-Substituted 1-Phenylethylamines from the Corresponding Acetophenones

Bringmann, Gerhard,Geisler, Joerg-Peter,Geuder, Torsten,Kuenkel, Georg,Kinzinger Lioba

, p. 795 - 805 (2007/10/02)

An efficient two-step procedure for the synthesis of enantiomerically pure, benzene nucleus-substituted 1-phenylethylamines 1 is described, with predictable absolute configuration at the stereogenic center: Imine formation from the substituted acetophenones 6 with (S)- or (R)-1-phenylethylamine and subsequent hydrogenation of the resulting Schiff bases 8 over Raney nickel leads to the secondary amines 9 and 10 in high diastereoselectivities.These dibenzylamines are cleaved regioselectively, usually next to the less substituted aromatic ring, giving the desired chiral 1-phenylethylamines 1 in high yields and enantiomeric purities.Scope and limitations of this new and facile approach to the versatile building blocks 1 are reported.

Synthesis and activity of 5-(aminomethylene)-1,3-cyclohexanediones: Enolic analogues of γ-aminobutyric acid

Mann,Humblet,Chambon,Schlichter,Desarmenien,Feltz,Wermuth

, p. 1440 - 1446 (2007/10/02)

Eight 1,3-cyclohexanediones with an aminoalkyl side chain in the 5-position were synthesized as rigid enolic analogues of GABA (γ-aminobutyric acid). Biochemical investigations about their abilities to displace [3H]GABA and [3H]baclo

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