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4-(azetidin-3-yl)benzonitrile is a chemical compound with the molecular formula C11H10N2. It is a derivative of benzonitrile, featuring a four-membered azetidine ring fused to the benzene ring at the 4-position. 4-(azetidin-3-yl)benzonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It is a white to off-white crystalline solid, and its properties include a melting point of around 65-67°C. The compound is typically synthesized through various chemical reactions, such as the condensation of 4-aminobenzonitrile with ethyl acetoacetate followed by cyclization. Due to its reactivity and structural features, 4-(azetidin-3-yl)benzonitrile serves as an important intermediate in the development of new chemical entities with potential therapeutic or pesticidal properties.

7215-03-4

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7215-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7215-03-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7215-03:
(6*7)+(5*2)+(4*1)+(3*5)+(2*0)+(1*3)=74
74 % 10 = 4
So 7215-03-4 is a valid CAS Registry Number.

7215-03-4SDS

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 4-(azetidin-3-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names p-(3-Azetidinyl)benzonitrile

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 -
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More Details:7215-03-4 SDS

7215-03-4Upstream product

7215-03-4Downstream Products

7215-03-4Relevant academic research and scientific papers

Catalytic Enantioselective Intermolecular Desymmetrization of Azetidines

Wang, Zhaobin,Sheong, Fu Kit,Sung, Herman H. Y.,Williams, Ian D.,Lin, Zhenyang,Sun, Jianwei

supporting information, p. 5895 - 5898 (2015/05/27)

The first catalytic asymmetric desymmetrization of azetidines is disclosed. Despite the low propensity of azetidine ring opening and challenging stereocontrol, smooth intermolecular reactions were realized with excellent efficiency and enantioselectivity.

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