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1-(2-nitrophenyl)cyclopropane-1-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147644-06-2

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147644-06-2 Usage

Appearance

Yellow crystalline solid

Usage

Commonly used in the synthesis of various pharmaceutical and agricultural products

Structural components

Contains a cyclopropane ring and a nitrophenyl group

Functional group

Presence of a carbonitrile functional group

Versatility

Acts as a versatile building block for the production of other organic compounds

Applications

Known for potential applications in medicinal chemistry, development of new materials and technologies

Biological activities

Studied for potential as an antitumor and antiparasitic agent

Safety

Should be handled with caution due to its toxic and potentially hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 147644-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,4 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 147644-06:
(8*1)+(7*4)+(6*7)+(5*6)+(4*4)+(3*4)+(2*0)+(1*6)=142
142 % 10 = 2
So 147644-06-2 is a valid CAS Registry Number.

147644-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-nitrophenyl)cyclopropane-1-carbonitrile

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:147644-06-2 SDS

147644-06-2Relevant academic research and scientific papers

Formal Total Synthesis of (±)-Strictamine by [2,3]-Sigmatropic Stevens Rearrangements

Eckermann, Ruben,Breunig, Michael,Gaich, Tanja

, p. 3938 - 3949 (2017/03/27)

To date, more than 100 congeners of the akuammiline alkaloid family have been isolated. Their signature structural element is a methanoquinolizidine moiety, a cage-like scaffold structurally related to adamantane. The structural variations of the family members originate from oxidative processes that mostly trigger rearrangements of the methanoquinolizidine motif. The family of the akuammiline alkaloids is best represented by strictamine. It bears the least functionalized carbon skeleton of all family members without lacking the signature structural motifs. Herein, we report the formal synthesis of strictamine through a Stevens [2,3]-sigmatropic rearrangement as a key step and the synthetic pitfalls related with its synthesis.

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