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57129-74-5

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57129-74-5 Usage

Class

Isoquinolinium salts

Type

Quaternary ammonium compound

Methoxy groups

Four

Methyl group

One

Attachment

Attached to the isoquinolinium ring

Form

Salt form as an iodide salt

Potential applications

Organic chemistry and pharmaceuticals

Unique features

Structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 57129-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,2 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 57129-74:
(7*5)+(6*7)+(5*1)+(4*2)+(3*9)+(2*7)+(1*4)=135
135 % 10 = 5
So 57129-74-5 is a valid CAS Registry Number.

57129-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,10,11-tetramethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium,iodide

1.2 Other means of identification

Product number -
Other names 2,3,10,11-tetramethoxy-7-methyl-berbinium,iodide

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:57129-74-5 SDS

57129-74-5Relevant articles and documents

LC-NMR and LC-MS analysis of 2,3,10,11-oxygenated protoberberine metabolites in Corydalis cell cultures

Isawa, Kinuko,Kuribayashi, Ayako,Sugiura, Makiko,Moriyasu, Masataka,Lee, Dong-Ung,Wiegrebe, Wolfgang

, p. 1229 - 1238 (2007/10/03)

The metabolism of 2,3,10,11-oxygenated protoberberine alkaloids was studied in cell cultures of Corydalis species. Without prior isolation, the structures of the metabolites were determined by LC-MS and LC-NMR analyses. Tetrahydropseudocoptisine α-N-metho salt, pseudoprotopine, and pseudomuramine were identified for the first time, and preliminary evidence for metabolic pathways to the formation of these alkaloids were obtained.

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