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2-[(E)-2-nitroethenyl]quinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68311-65-9

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68311-65-9 Usage

Family

Quinoline

Functional Groups

Nitro Group (NO2)
Ethenyl Group (C2H3)

Application in Organic Chemistry

Used as a building block for synthesizing various molecules and pharmaceuticals.

Potential Applications

Drug Development: Utilized in the creation of new drugs.
Agrochemicals: Potential applications in the development of agrochemicals.

Biological Activities

Studied for potential biological activities.

Interest Areas

Medicinal Chemistry
Chemical Biology

Check Digit Verification of cas no

The CAS Registry Mumber 68311-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,1 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68311-65:
(7*6)+(6*8)+(5*3)+(4*1)+(3*1)+(2*6)+(1*5)=129
129 % 10 = 9
So 68311-65-9 is a valid CAS Registry Number.

68311-65-9SDS

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-[(E)-2-nitroethenyl]quinoline

1.2 Other means of identification

Product number -
Other names -

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:68311-65-9 SDS

68311-65-9Relevant academic research and scientific papers

A convenient 1,3-dipolar cycloaddition approach to pyridylpyrroles

Lopchuk, Justin M.,Gribble, Gordon W.

scheme or table, p. 4106 - 4108 (2011/09/19)

A variety of 2-, 3-, and 4-pyridylpyrroles were synthesized in good to excellent yields via the 1,3-dipolar cycloaddition of symmetrical and unsymmetrical muenchnones and nitroalkenes. The unsymmetrical muenchnones show moderate to excellent regioselectiv

Synthesis and molluscicidal activity evaluation of some nitroquinolines.

Shoeb,Korkor,Tammam

, p. 581 - 583 (2007/10/08)

Synthesis of some nitroquinoline acrylamides, nitrovinylquinolines and quinoline Mannich bases has been carried out. Screening of the synthesized compounds for molluscicidal activity is reported.

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