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3,3-diphenylazetidine is a chemical compound with the molecular formula C16H15N. It is a cyclic amine, specifically an azetidine derivative, which features a four-membered nitrogen-containing ring structure. The two phenyl groups attached to the nitrogen atom give 3,3-diphenylazetidine its unique structure and properties. 3,3-diphenylazetidine is an important intermediate in the synthesis of various pharmaceuticals and organic compounds due to its stability and reactivity. It is typically synthesized through various methods, such as the reaction of phenylmagnesium bromide with N-tosylaziridine or the intramolecular cyclization of 1,2-diphenylethene-1,2-diamine. The compound is known for its potential applications in the development of new drugs and materials, as well as its role in organic chemistry research.

7215-23-8

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7215-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7215-23-8 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7215-23:
(6*7)+(5*2)+(4*1)+(3*5)+(2*2)+(1*3)=78
78 % 10 = 8
So 7215-23-8 is a valid CAS Registry Number.

7215-23-8SDS

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 3,3-diphenylazetidine

1.2 Other means of identification

Product number -
Other names L 1964

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:7215-23-8 SDS

7215-23-8Downstream Products

7215-23-8Relevant academic research and scientific papers

A NOVEL SYNTHESIS OF 3,3-(SPIRO)SUBSTITUTED AZETIDINES

Froehlich, Johannes,Sauter, Fritz,Blasl, Karin

, p. 1879 - 1892 (2007/10/02)

A smooth and efficient new synthesis for 3,3-disubstituted azetidines, starting from readily available nitriles, was estabilished: α-hydroxymethylation of the starting materials, followed by O-tosylation and LiAlH4-reduction of the key intermediates thus obtained, led - via spontaneous cyclization of the intermediate amino derivatives - to 3,3-disubstituted azetidines.Scope and limitations of this new method were studied with respect to generalized applicability: the target compounds were accessible in good yields for a variety of starting materials (cyclic and acyclic di(hetero)aryl, (hetero)arylalkyl, dialkyl, as well as basic moieties).The products thus obtained may be of interest for ensuing conversions due to their unblocked nitrogen.

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