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2-[1-(4-bromophenyl)ethylidene]-1,1-dimethylhydrazine is an organic compound with the chemical formula C10H13BrN2. It is a derivative of hydrazine, featuring a 4-bromophenyl group attached to an ethylidene bridge, which is in turn connected to a dimethylhydrazine moiety. 2-[1-(4-bromophenyl)ethylidene]-1,1-dimethylhydrazine is characterized by its potential reactivity due to the presence of the bromine atom, which can participate in various chemical reactions such as substitution or addition reactions. It is important to handle 2-[1-(4-bromophenyl)ethylidene]-1,1-dimethylhydrazine with care, as it may have toxicological properties and could be harmful if not properly managed. The compound's structure and reactivity make it a potential candidate for use in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals where its unique functional groups can be exploited.

5757-83-5

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5757-83-5 Usage

Chemical compound

2-[1-(4-bromophenyl)ethylidene]-1,1-dimethylhydrazine

Properties

dimethylhydrazine derivative with a bromophenyl group and an ethylidene side chain
Commonly used in research and laboratory settings
Potential use in pharmaceutical drug discovery and development
Ability to interact with biological systems
Must be handled with caution due to potential risks to human health and the environment
Potential applications in organic chemistry and material science due to structural properties

Check Digit Verification of cas no

The CAS Registry Mumber 5757-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5757-83:
(6*5)+(5*7)+(4*5)+(3*7)+(2*8)+(1*3)=125
125 % 10 = 5
So 5757-83-5 is a valid CAS Registry Number.

5757-83-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-8-methyl-quinoline

1.2 Other means of identification

Product number -
Other names p-Bromoacetophenone N,N-dimethylhydrazone

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:5757-83-5 SDS

5757-83-5Relevant academic research and scientific papers

Synthesis of isoquinolines via Rh(III)-catalyzed C-H activation using hydrazone as a new oxidizing directing group

Chuang, Sheng-Chieh,Gandeepan, Parthasarathy,Cheng, Chien-Hong

supporting information, p. 5750 - 5753 (2013/12/04)

An efficient and mechanistically interesting method for the synthesis of highly substituted isoquinolines by a Rh(III)-catalyzed hydrazone directed ortho C-H bond activation and annulation without an external oxidant is described. This reaction is accomplished via a C-C and C-N bond formation along with N-N bond cleavage.

Highly efficient Narasaka-Heck cyclizations mediated by P(3,5-(CF 3)2C6H3)3: Facile access to N-heterobicyclic scaffolds

Faulkner, Adele,Bower, John F.

supporting information; experimental part, p. 1675 - 1679 (2012/04/05)

N-heterobicyclic scaffolds: Highly efficient palladium-catalyzed cyclizations of oxime esters with cyclic alkenes were used as a general entry to perhydroindole and related scaffolds. The chemistry is reliant upon the use of P(3,5-(CF3)2/

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