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Bis-(dimethylmaleic)-hydrazide is a chemical compound that is primarily used in the field of organic chemistry. It likely features properties typical to other hydrazides and derivatives of maleic acid, including its use as a reagent to help facilitate, or act as a catalyst in, chemical reactions.

6903-84-0

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6903-84-0 Usage

Uses

Used in Organic Chemistry:
Bis-(dimethylmaleic)-hydrazide is used as a reagent for facilitating or acting as a catalyst in chemical reactions. Its properties, similar to other hydrazides and derivatives of maleic acid, make it a valuable component in various organic chemistry processes.
It’s always recommended to work with such compounds in a controlled environment following all safety protocols to ensure safe handling and use.

Check Digit Verification of cas no

The CAS Registry Mumber 6903-84-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6903-84:
(6*6)+(5*9)+(4*0)+(3*3)+(2*8)+(1*4)=110
110 % 10 = 0
So 6903-84-0 is a valid CAS Registry Number.

6903-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [1,1'-Bipyrrole]-2,2',5,5'-tetraone

1.2 Other means of identification

Product number -
Other names 1-(2,5-dioxopyrrol-1-yl)pyrrole-2,5-dione

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:6903-84-0 SDS

6903-84-0Upstream product

6903-84-0Relevant academic research and scientific papers

Three-Component Synthesis of Quinolines Based on Radical Cascade Visible-Light Photoredox Catalysis

Choi, Jun-Ho,Park, Cheol-Min

supporting information, p. 3553 - 3562 (2018/09/22)

Synthesis of highly substituted quinolines has been developed based on three-component radical cascade based on visible-light photoredox catalysis. This tandem coupling reaction has been coordinated to proceed with high chemoselectivity based on the differential electronic properties of coupling partners. Subjection of electron-rich β-aminoacrylates with electron-deficient halides and alkenes to the optimized conditions leads to the formation of quinolines in good yields after in situ oxidation of tetrahydroquinolines. Detailed mechanistic studies which reveal an unexpected reaction pathway is described. (Figure presented.).

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