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Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI), also known as alpha-ethyl-2-methoxyphenethylamine, is a chemical compound with the molecular formula C10H15NO. It is a derivative of phenethylamine and is classified as a psychoactive drug. Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI) is an enantiomer of the chemical structure, meaning it has a chiral center and exists in two different mirror-image forms. Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI) is commonly used for its stimulant and psychedelic effects, and is considered a controlled substance in many countries due to its potential for abuse and addiction. Research on the effects and safety of Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)- (9CI) is ongoing, and its use is regulated in many jurisdictions.

623143-38-4

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623143-38-4 Usage

Uses

Used in Pharmaceutical Industry:
Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI) is used as an active pharmaceutical ingredient for its stimulant and psychedelic effects. It is utilized in the development of medications targeting specific neurological conditions and disorders.
Used in Research Applications:
In the field of scientific research, Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI) is used as a research chemical to study its effects on the central nervous system and to understand its potential therapeutic applications and safety profile.
Used in Controlled Substances Regulation:
Due to its potential for abuse and addiction, Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)(9CI) is used as a reference compound in the development and enforcement of regulations and policies related to controlled substances in various jurisdictions.

Check Digit Verification of cas no

The CAS Registry Mumber 623143-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,4 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 623143-38:
(8*6)+(7*2)+(6*3)+(5*1)+(4*4)+(3*3)+(2*3)+(1*8)=124
124 % 10 = 4
So 623143-38-4 is a valid CAS Registry Number.
InChI:InChI=1S/C10H15NO/c1-3-9(11)8-6-4-5-7-10(8)12-2/h4-7,9H,3,11H2,1-2H3/t9-/m1/s1

623143-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1-(2-Methoxyphenyl)propan-1-amine hydrochloride

1.2 Other means of identification

Product number -
Other names (1R)-1-(2-methoxyphenyl)propan-1-amine,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:623143-38-4 SDS

623143-38-4Relevant academic research and scientific papers

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

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Page/Page column 34, (2011/04/14)

A 10a-azalide compound having a 4-membered ring structure crosslinked at the 10a- and 12-positions, which is represented by the formula (I), and is effective on even Haemophilus influenzae, or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).

Efficient dual catalytic enantioselective diethylzinc addition to the exocyclic C{double bond, long}N double bond of some 1,2,4-N-triazinylarylimines using polymer-supported chiral β-amino alcohols derived from norephedrine

El-Shehawy, Ashraf A.

, p. 5490 - 5500 (2008/01/07)

Chiral N,N-dialkylnorephedrines and their corresponding copolymers were evaluated as chiral ligands for the enantioselective diethylzinc addition to the exocyclic C{double bond, long}N double bond of some 4-arylideneamino-3-mercapto-6-methyl-4H-1,2,4-triazin-5-ones 2a-f. The use of a dual catalytic system (amino alcohol/halosilane) in the titled asymmetric reaction was examined. The enantioselective ethylation reaction has been successfully carried out in the heterogeneous system even at low temperature. The corresponding 4-(1-arylpropyl)amino-3-mercapto-6-methyl-4H-1,2,4-triazin-5-ones 4a-f were obtained in high yields with high enantioselectivities using chiral polymers (up to 91% ee), which are almost the same as those obtained from homogeneous analogues (up to 92% ee). The diethylzinc reagent neither opened the 1,2,4-triazinyl heterocyclic ring nor attacked the carbonyl or the thione groups of the 1,2,4-triazinyl heterocyclic ring and the addition reaction took place exclusively at the exocyclic electrophilic carbon atom yielding the C-ethylated products 4a-f. Reductive cleavage of the 1,2,4-triazinyl heterocyclic ring led smoothly to the corresponding primary aromatic amines 11a-f without significant loss of enantiomeric purity. A?suggestion about the possible transition state for the addition reaction is also presented.

Enantioselective diethylzinc addition to the exocyclic C{double bond, long}N double bond of some 4-arylideneamino-3-mercapto-6-methyl-4H-1,2,4-triazin-5-one derivatives

El-Shehawy, Ashraf A.

, p. 2617 - 2624 (2007/10/03)

4-Arylideneamino-3-mercapto-6-methyl-4H-1,2,4-triazin-5-ones 2a-f have been evaluated as substrates in the enantioselective diethylzinc addition reaction in the presence of (1S,2R)-N-alkyl-N-benzylnorephedrines 3a-d as chiral ligands. The utility of using a dual catalytic system (amino alcohol/halosilane) for the diethylzinc addition reaction has been also examined. The addition products 4-(1-arylpropyl)amino-3-mercapto-6-methyl-4H-1,2,4-triazin-5-ones 4a-f were obtained in high yields and with enantiomeric excesses of up to 92%. The treatment of arylimines 2a-f with a diethylzinc reagent did not affect the hetero-ring opening although the C{double bond, long}N double bond of the lateral chain did undergo an addition reaction to yield the C-ethylated products 4a-f. The reductive cleavage of the 1,2,4-triazinyl heterocyclic ring from addition products 4a-f led smoothly to the corresponding free primary amines 5a-f without a significant loss of enantiomeric purity.

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