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1-[3-(ethylsulfanyl)-5,5-dimethylcyclohex-2-en-1-ylidene]pyrrolidinium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80348-35-2

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80348-35-2 Usage

Molecular structure

The compound has a complex molecular structure with a pyrrolidinium core attached to a cyclohexene ring.

Substituents

The cyclohexene ring is substituted with an ethylsulfanyl group and two methyl groups.

Positioning of groups

The specific positioning of the substituents around the pyrrolidinium core gives the molecule its unique properties.

Potential applications

The compound may have potential applications in fields such as organic synthesis, medicinal chemistry, and materials science due to its unique structure and potential reactivity.

Further research

Further research and study will be necessary to fully understand and exploit the potential of this unique molecule.

Check Digit Verification of cas no

The CAS Registry Mumber 80348-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,4 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80348-35:
(7*8)+(6*0)+(5*3)+(4*4)+(3*8)+(2*3)+(1*5)=122
122 % 10 = 2
So 80348-35-2 is a valid CAS Registry Number.

80348-35-2SDS

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-(3-ethylsulfanyl-5,5-dimethylcyclohex-2-en-1-ylidene)pyrrolidin-1-ium,iodide

1.2 Other means of identification

Product number -
Other names -

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:80348-35-2 SDS

80348-35-2Relevant academic research and scientific papers

α,β-UNSATURATED THIO COMPOUNDS. XIII.* HYDROTHIOLYSIS OF β-HETERO-SUBSTITUTED α,β-UNSATURATED IMMONIUM SALTS AT THE C=N(+) BOND - A GENERAL APPROACH TO THE SYNTHESIS OF FUNCTIONALLY SUBSTITUTED THIOKETONES

Usov, V. A.,Timokhina, L. V.,Zhagun, V. A.,Sidorkin, V. F.,Voronkov, M. G.

, p. 1623 - 1628 (2007/10/02)

The hydrothiolysis of immonium salts containing the Y-C=C-C=N(+) group takes place at the C=N(+) bond and not at the C-Y bond.This is consistent with the results from quantum-chemical calculations.On this basis a general approach was formulated to the synthesis of new types of organic sulfur compounds, i.e. β-alkoxy-, β-alkylthio-, and β-halogen-substituted α,β-unsaturated thioketones of the Y-C=C-C=S (Y=RO, RS, Hlg) type.

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