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1-(Cyclohex-1-en-1-yl)azetidine is a chemical compound with the molecular formula C9H15N. It is a heterocyclic compound, featuring a cyclohexene ring fused to an azetidine ring, which is a four-membered nitrogen-containing ring. 1-(cyclohex-1-en-1-yl)azetidine is of interest in organic chemistry due to its unique structure and potential applications in the synthesis of various pharmaceuticals and agrochemicals. The cyclohexene ring provides a stable, rigid framework, while the azetidine ring introduces a reactive nitrogen center, making 1-(cyclohex-1-en-1-yl)azetidine a versatile building block for the development of new molecules with specific biological activities.

7326-44-5

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7326-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7326-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7326-44:
(6*7)+(5*3)+(4*2)+(3*6)+(2*4)+(1*4)=95
95 % 10 = 5
So 7326-44-5 is a valid CAS Registry Number.

7326-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(cyclohexen-1-yl)azetidine

1.2 Other means of identification

Product number -
Other names 1-Azetidinocyclohexene

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:7326-44-5 SDS

7326-44-5Relevant academic research and scientific papers

178. Stereoselectivity of the Radical Reductive Alkylation of Enamines: Importance of the Allylic 1,3-Strain Model

Schubert, Serge,Renaud, Philippe,Carrupt, Pierre-Alain,Schenk, Kurt

, p. 2473 - 2489 (2007/10/02)

Radical addition to enamines using Bu3SnH as reducing agent are reported (Schemes 2 and 4).The diastereoselectivity of these reactions was examined in different systems (Tables 1 and 2).Enamines derived from cyclic ketones such as cyclohexanone were alkyl

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