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2,2'-(cyclohexane-1,1-diyl)bis(1H-pyrrole) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35303-46-9

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35303-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35303-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,0 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35303-46:
(7*3)+(6*5)+(5*3)+(4*0)+(3*3)+(2*4)+(1*6)=89
89 % 10 = 9
So 35303-46-9 is a valid CAS Registry Number.

35303-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-(cyclohexane-1,1-diyl)bis(1H-pyrrole)

1.2 Other means of identification

Product number -
Other names 1,1'-di-(α-pyrrolyl)cyclohexane

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:35303-46-9 SDS

35303-46-9Relevant academic research and scientific papers

Effects of 5,5-substitution on dipyrrolylmethane ligand isomerization

Swartz II, Douglas L.,Odom, Aaron L.

, p. 4254 - 4258 (2008)

The difference in steric profiles for η5 and η1-pyrrolyls can be used to modify barriers for pyrrolyl exchange. The method investigated incorporated 1,3-diaxial interactions in a cyclohexyl backbone of the dipyrrolylmethane. Some of the enthalpic barrier created with the 1,3-steric interactions appears to be mediated by increased entropy in the ground state, but noticeable changes are produced in the pyrrolyl exchange rates by 1H NMR without steric crowding at the metal center.

Use of graphite oxide and graphene oxide as catalysts in the synthesis of dipyrromethane and calix[4]pyrrole

Singh Chauhan, Shive Murat,Mishra, Sweta

, p. 7256 - 7266 (2011)

Graphite oxide and graphene oxides have been used as solid catalysts for the synthesis of 5,5-dialkyldipyrromethanes and calix[4]pyrroles in organic and aqueous solutions at room temperature.

Dipyrromethane as a new organic reagent for the synthesis of gold nanoparticles: Preparation and application

Eshghi,Rahimizadeh,Attaran,Bakavoli

, p. 1151 - 1157 (2013/11/06)

Condensation reaction of several ketones with pyrrole in the presence of ferric hydrogen sulfate as a green homogenous acidic catalyst furnished the corresponding pure dipyrromethanes in good yields. Gold nanoparticles were produced through reduction of H

Highly efficient synthesis of N-confused meso-tetraspirocyclohexyl calix[4]pyrrole using Bronsted acidic ionic liquids as catalysts

Garg, Bhaskar,Ling, Yong-Chien

, p. 5674 - 5677 (2012/11/07)

An efficient, green and novel protocol is described for high yield synthesis of N-confused meso-tetraspirocyclohexyl calix[4]pyrrole. In aqueous solution, the condensation of pyrrole and cyclohexanone in the presence of Bronsted acidic ionic liquid catalysts afforded N-confused calix[4]pyrrole in up to 62.5% yield which represents a ~threefold yield improvement over existing protocol and makes significant quantity of N-confused calix[4]pyrrole readily available.

A novel, shape-selective, zeolite-catalyzed synthesis of calix(4)pyrroles

Kishan, M. Radha,Srinivas, N.,Raghavan, K. V.,Kulkarni, S. J.,Sarma, J. A. R. P.,Vairamani, M.

, p. 2226 - 2227 (2007/10/03)

Porosity and acidity of molecular sieve Al-MCM-41 (ca. 30 Angstroem pore diameter) plays a crucial role in the synthesis of novel calix(4)pyrroles; for the first time, Al-MCM-41 has been used as a solid acid catalyst to produce a number of calix(4)pyrroles with good selectivity and yields where zeolite HY (ca. 7.6 Angstroem pore diameter) yields mainly the linear chain dimer and no cyclic products.

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