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623143-38-4

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623143-38-4 Usage

General Description

Benzenemethanamine, alpha-ethyl-2-methoxy-, (alphaR)- (9CI) is a chemical compound with the molecular formula C10H15NO. Also known as alpha-ethyl-2-methoxyphenethylamine, 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. It 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 this compound is ongoing, and its use is regulated in many 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 articles and documents

10A-AZALIDE COMPOUND HAVING 4-MEMBERED RING STRUCTURE

-

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).

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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