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2305-54-6

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2305-54-6 Usage

Usage

Used in various industrial and research applications

Building block

Utilized in organic synthesis and production of pharmaceuticals, agrochemicals, and other chemical products

Reagent

Potential as a reagent in creating new materials and molecular structures

Pharmaceutical industry

Useful component for synthesis of potential drug candidates and biologically active compounds

Role in organic chemistry

Plays a significant role and has wide range of potential applications in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 2305-54-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2305-54:
(6*2)+(5*3)+(4*0)+(3*5)+(2*5)+(1*4)=56
56 % 10 = 6
So 2305-54-6 is a valid CAS Registry Number.

2305-54-6SDS

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-(Anilinomethylen)-2-cyanessigsaeure-ethylester

1.2 Other means of identification

Product number -
Other names 3-Anilino-2-cyan-acrylsaeure-aethylester

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:2305-54-6 SDS

2305-54-6Relevant articles and documents

Efficient and selective construction of pyrrolo[3,2-d]pyrimidine derivatives

He, Ping,Wu, Jing,Hu, Yang-Gen,Li, Zai-Fang,Hou, Qiu-Fei,Wang, Yan-Ling,Zhao, Kun,Zhang, Erli

, p. 617 - 621 (2014/03/21)

An efficient and selective method for the synthesis of ethyl 2-amino/aryloxy-3-aryl-4-oxo-5-phenyl-4,5-dihydro-3H-pyrrolo[3,2-d] pyrimidine-7-carboxylate derivatives has been developed. The main process involved the reaction of diethyl 1-phenyl-3-((triphe

Microwave-assisted simple synthesis of substituted 4-quinolone derivatives

Cao, Xin,You, Qi-Dong,Li, Zhi-Yu,Yang, Yan,Wang, Xiao-Jian

experimental part, p. 4375 - 4383 (2010/05/01)

A simple and efficient method was developed for the synthesis of 4-quinolone-3-carboxylic esters and 4-quinolone-3-carbonitriles under microwave (MW) activation using anilines and acrylates as materials. All reactions demonstrated the benefits of microwave reactions: convenient operation, short reaction time, and good yields.

Derivatives of quinoline as alpha-2 antagonists

-

, (2008/06/13)

A compound of formula I, wherein A, Ra, Rb, R1 to R5, m and t are as defined as disclosed, or a pharmaceutically acceptable salt or ester thereof, useful as an alpha-2 antagonist. The compounds I can be used for the treatment of diseases or conditions where alpha-2 antagonists are indicated to be effective.

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