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56517-31-8

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56517-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56517-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,1 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56517-31:
(7*5)+(6*6)+(5*5)+(4*1)+(3*7)+(2*3)+(1*1)=128
128 % 10 = 8
So 56517-31-8 is a valid CAS Registry Number.

56517-31-8SDS

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-Bromo-4-ethoxy-5-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-ethoxy-2-bromo-5-methoxy-benzaldehyde

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:56517-31-8 SDS

56517-31-8Relevant academic research and scientific papers

Synthesis of N-Substituted Condensed Tetrahydropyridine-Based Enaminones via Palladium-Catalyzed Intramolecular C–N Cross-coupling

Dou?ová, Hana,R??i?ková, Zdeňka,?im?nek, Petr

, p. 670 - 684 (2018/01/22)

A number of β-enaminones with secondary amino group (alkyl, cyclopropyl, and aryl) were prepared from corresponding β-diketones. Two general protocols for their palladium-catalyzed intramolecular C–N cross-coupling were established to give corresponding N-substituted condensed tetrahydropyridines in good yields. The methodology is applicable for a wide variety of structural motifs. The work also extends the applicability of novel, recently established, palladium precatalysts to new substrates.

Synthesis and biological activity of some antitumor benzophenanthridinium salts

Stermitz,Gillespie,Amoros,Romero,Stermitz,Larson,Earl,Ogg

, p. 708 - 713 (2007/10/05)

A facile synthesis of benzophenanthridinium salts was developed and used for preparing a number of these compounds. The antitumor activities in mouse leukemia L1210 (LE) and P388 (PS) were determined as well as some selected antimicrobial activities. Alth

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