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Benzenemethanol, 2-(2,5-dimethyl-1H-pyrrol-1-yl)-, also known as 2-(2,5-dimethyl-1H-pyrrol-1-yl)benzenemethanol, is an organic compound with the molecular formula C12H15NO. It is a derivative of benzenemethanol, featuring a 2,5-dimethyl-1H-pyrrole group attached to the benzene ring. Benzenemethanol, 2-(2,5-dimethyl-1H-pyrrol-1-yl)- is characterized by its unique chemical structure, which consists of a benzene ring with a hydroxyl group (-OH) attached to the 2nd carbon, and a 2,5-dimethyl-1H-pyrrole ring fused to the benzene ring. The presence of the pyrrole ring and the methyl groups on the pyrrole ring contribute to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.

97690-10-3

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97690-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97690-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,9 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97690-10:
(7*9)+(6*7)+(5*6)+(4*9)+(3*0)+(2*1)+(1*0)=173
173 % 10 = 3
So 97690-10-3 is a valid CAS Registry Number.

97690-10-3SDS

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 [2-(2,5-dimethylpyrrol-1-yl)phenyl]methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,2-(2,5-dimethyl-1H-pyrrol-1-yl)

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:97690-10-3 SDS

97690-10-3Relevant academic research and scientific papers

N-(2-Methylinden-4-yl)pyrrole as a heterocyclic analog of 2-methyl-4-arylindene. Synthesis of [μ-SiMe2(η5-2- Me-4-(2,4-Me2C4H2N)Ind)2]ZrCl 2

Ivchenko,Ivchenko,Nifant'Ev

experimental part, p. 589 - 593 (2010/08/08)

A unique strategy for the synthesis of 2-methyl-4-arylindenes was tested for 1-(4-indenyl)- pyrrole. The procedure includes the Paal-Knorr synthesis of a nonsymmetric arylhetaryl fragment followed by intramolecular acylation. The zirconium complex of the

Spectroscopic Study of Some New N-Aryl Pyrroles

Saeed, Ali A. H.

, p. 498 - 499 (2007/10/02)

A series of new 2,5-dimethyl-N-substituted pyrroles (I) were obtained by condensation of 2,5-hexanedione with different amines.The UV data show that about 11.7percent of the total electronic density of the nitrogen of pyrrole ring is conjugated with the aryl group.A correlation between the UV and NMR results has been established, and the mass spectra of these derivatives have also been measured and discussed.

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