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Azetidine, 1-(phenylmethyl)-, also known as 1-benzylaziridine, is a chemical compound with the molecular formula C9H13N. It is a cyclic amine, specifically a three-membered nitrogen-containing ring, with a benzyl group attached to the nitrogen atom. Azetidine, 1-(phenylmethyl)- is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique structure and reactivity. It can be synthesized through various methods, such as the reaction of benzyl chloride with sodium azide or the intramolecular cyclization of α-amino acids. 1-Benzylaziridine is known for its ability to undergo ring-opening reactions, making it a valuable building block in organic synthesis.

7730-39-4

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7730-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7730-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7730-39:
(6*7)+(5*7)+(4*3)+(3*0)+(2*3)+(1*9)=104
104 % 10 = 4
So 7730-39-4 is a valid CAS Registry Number.

7730-39-4Relevant academic research and scientific papers

Microwave-assisted synthesis of azetidines in aqueous media

Burkett, Brendan A.,Ting, Samuel Z.,Gan, Gwendolyn C. S.,Chai, Christina L. L.

supporting information; experimental part, p. 6590 - 6592 (2011/02/23)

Simple azetidines are synthesized in good to excellent yields and high purity via cyclization of 3-(ammo-nio)propyl sulfates derived from primary amines and the cyclic sulfate of 1,3-propanediol. A feature of this methodology includes the accelerated synt

Mechanistic considerations for the consecutive cyclization of 2,3-dibromopropylamine hydrobromide giving a strained molecule, 1-azabicyclo[1.1.0]butane

Hayashi, Kazuhiko,Ikee, Yoshifumi,Goto, Satoru,Shiro, Motoo,Nagao, Yoshimitsu

, p. 89 - 94 (2007/10/03)

The effective formation of 1-azabicyclo[1.1.0]butane (2) by treatment of 2,3-dibromopropylamine hydrobromide (1) with n-BuLi could be understood considering a rational reaction pathway via both transition states 10 and 19 based on the intramolecular Br...

A facile and efficient synthesis of N-benzylazetidine

Lai

, p. 565 - 568 (2007/10/03)

An efficient, two-step synthesis of N-benzylazetidine, starting from benzaldehyde and 3-bromopropylamine hydrobromide, is described.

Synthesis of aziridines and acetidines from N-(ω-haloalkyl) imines

De Kimpe,De Smaele

, p. 8023 - 8026 (2007/10/02)

N-(2-haloalkyl) and N-(3-haloalkyl) imines are convenient substrates for the synthesis of aziridines and azetidines via a two-step process involving nucleophile induced addition at the imino bond followed by intramolecular nucleophilic substitution.

Preparation of Azetidines from 1,3-Aminopropanols

Sammes, Peter G.,Smith, Steven

, p. 2415 - 2420 (2007/10/02)

The preparation of 1,3-amino alcohols by the reduction of azetidin-2-ones with diborane is described.New methods for the cyclisation of the aminopropanols to the corresponding azetidines are reported; these methods centre on the use of a modified Mitsunobu reaction.

On the Synthesis of Azetidines from 3-Hydroxypropylamines

Sammes, Peter G.,Smith, Steven

, p. 682 - 684 (2007/10/02)

New methods are described for preparing azetidines from 3-hydroxypropylamines involving the use of triphenylphosphine and diethyl azodicarboxylate and related reagents.

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