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1-Benzyl-3-phenylazetidine is a chemical compound with the molecular formula C16H17N. It is a derivative of azetidine, a four-membered heterocyclic ring containing one nitrogen atom. The structure of 1-Benzyl-3-phenylazetidine features a benzyl group (C6H5CH2-) attached to the nitrogen atom at position 1 and a phenyl group (C6H5-) attached to the carbon atom at position 3. 1-Benzyl-3-phenylazetidine is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be synthesized through various methods, such as the reaction of benzylamine with phenylacetonitrile or the cyclization of 1-phenyl-2-benzylaziridine. The compound is typically used as a building block in the preparation of more complex molecules, showcasing its versatility in organic chemistry.

7215-16-9

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7215-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7215-16-9 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, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7215-16:
(6*7)+(5*2)+(4*1)+(3*5)+(2*1)+(1*6)=79
79 % 10 = 9
So 7215-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H17N/c1-3-7-14(8-4-1)11-17-12-16(13-17)15-9-5-2-6-10-15/h1-10,16H,11-13H2

7215-16-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-3-phenylazetidine

1.2 Other means of identification

Product number -
Other names AZETIDINE,1-BENZYL-3-PHENYL

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:7215-16-9 SDS

7215-16-9Downstream Products

7215-16-9Relevant academic research and scientific papers

Anti-Markovnikov rearrangement in sulfur mediated allylic C-H amination of olefins

Zhang, Zhong,Du, Hongguang,Xu, Jiaxi,Li, Pingfan

supporting information, p. 11547 - 11550 (2016/10/03)

Cationic rearrangement reactions usually follow Markovnikov's rule to give more substituted carbocations as stable intermediates. During our study on sulfur mediated allylic C-H amination of olefins, very rare cases of anti-Markovnikov rearrangement from secondary carbocations toward primary carbocations or primary triflates were observed.

A one-pot preparation of 1,3-disubstituted azetidines

Hillier, Michael C.,Chen, Cheng-Yi

, p. 7885 - 7887 (2007/10/03)

(Chemical Equation Presented) A straightforward synthesis of 1,3-disubstituted azetidines has been accomplished via the alkylation of a primary amine with the bis-triflate of a 2-substituted-1,3-propanediol species. This transformation is carried out in o

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