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5096-82-2

Isoquinolinium, 3,4-dihydro-6,7-dimethoxy-2-(phenylmethyl)-, bromide is a complex organic compound with the chemical formula C19H20BrNO2. It is a derivative of isoquinolinium, a heterocyclic compound with a benzene ring fused to a pyridine ring. The molecule features a 3,4-dihydro structure, which means it has two hydrogen atoms added to the isoquinolinium ring, reducing its aromaticity. The 6 and 7 positions on the ring are occupied by methoxy groups (-OCH3), which are electron-donating groups that can influence the compound's reactivity and solubility. The 2 position is substituted with a phenylmethyl group (C6H5-CH2-), which introduces a phenyl ring and a methyl group, further enhancing the compound's structural complexity. The bromide ion (Br-) is associated with the cationic isoquinolinium moiety, making the overall compound a salt. This chemical is likely to be used in research settings, particularly in the synthesis of pharmaceuticals or other organic compounds, due to its unique structure and potential reactivity.

5096-82-2

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5096-82-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5096-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5096-82:
(6*5)+(5*0)+(4*9)+(3*6)+(2*8)+(1*2)=102
102 % 10 = 2
So 5096-82-2 is a valid CAS Registry Number.

5096-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzyl-6,7-dimethoxy-3,4-dihydroisoquinolin-2-ium,bromide

1.2 Other means of identification

Product number -
Other names 2-benzyl-6,7-dimethoxy-3,4-dihydro-isoquinolinium bromide

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:5096-82-2 SDS

5096-82-2Relevant articles and documents

A facile synthesis of novel polycyclic spiropyrrolidine oxindoles incorporating the 1,3-dipolar cycloaddition of azomethine ylides

Treuerne Balázs, Krisztina E.,Molnár, Márk,Madarász, Zoltán,Nyerges, Miklós

supporting information, p. 3245 - 3255 (2020/08/06)

This study describes the synthesis of novel polycyclic spiropyrrolidine oxindoles through the 1,3-dipolar cycloaddition of azomethine ylides generated in situ with 3-(arylmethylene)-indolin-2-ones. Effect of substituents of azomethine ylides and various d

A new enlargement methodology for the preparation of 2H-1- and 2H-3-benzazepin-2-one derivatives

Jean-Gérard, Ludivine,Pauvert, Micka?l,Collet, Sylvain,Guingant, André,Evain, Michel

, p. 11250 - 11259 (2008/03/12)

An investigation of the one-carbon homologation of some 1-tribromomethyl-isoquinoline and 2-tribromomethyl-quinoline derivatives was conducted. Under the influence of an aqueous solution of silver nitrate in the presence of a nucleophilic species (MeOH, H

Silver nitrate-promoted ring enlargement of 1-tribromomethyl-1,2-dihydro- and 1-tribromomethyl-1,2,3,4-tetrahydro-isoquinoline derivatives: Application to the synthesis of the anti-anginal zatebradine

Pauvert, Micka?l,Collet, Sylvain,Guingant, André

, p. 4203 - 4206 (2007/10/03)

The one step AgNO3-mediated ring enlargement of 1-tribromomethyl-1,2-dihydro- and 1-tribromomethyl-1,2,3,4-tetrahydro-isoquinoline derivatives into 1,2-dihydro- and 1,2,3,4-tetrahydro-benzo[d]azepin-2-ones, respectively, is reported. This reaction offers a convenient entry to potentially active substances such as the anti-anginal zatebradine.

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