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50691-34-4

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50691-34-4 Usage

Chemical structure

A pyrrole ring with a phenethyl group and two methyl groups attached to the 2 and 5 positions

Uses

Commonly used in research and development of new drugs and pharmaceuticals

Medicinal properties

Potential as an antifungal agent and a therapeutic agent for various diseases

Unique features

Valuable for further investigation and potential applications in the pharmaceutical industry due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 50691-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,9 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50691-34:
(7*5)+(6*0)+(5*6)+(4*9)+(3*1)+(2*3)+(1*4)=114
114 % 10 = 4
So 50691-34-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17N/c1-12-8-9-13(2)15(12)11-10-14-6-4-3-5-7-14/h3-9H,10-11H2,1-2H3

50691-34-4SDS

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 2,5-dimethyl-1-(2-phenylethyl)pyrrole

1.2 Other means of identification

Product number -
Other names 2,5-dimethyl-1-phenethyl-pyrrole

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:50691-34-4 SDS

50691-34-4Relevant articles and documents

Volatiles from the Psychrotolerant Bacterium Chryseobacterium polytrichastri

Lauterbach, Lukas,Dickschat, Jeroen S.

, p. 3608 - 3617 (2020/09/22)

The flavobacterium Chryseobacterium polytrichastri was investigated for its volatile profile by use of a closed-loop stripping apparatus (CLSA) and subsequent GC-MS analysis. The analyses revealed a rich headspace extract with 71 identified compounds. Compound identification was based on a comparison to library mass spectra for known compounds and on a synthesis of authentic standards for unknowns. Important classes were phenylethyl amides and a series of corresponding imines and pyrroles.

Chemoselective Synthesis of Amines from Ammonium Hydroxide and Hydroxylamine in Continuous Flow

Audubert, Clément,Bouchard, Alexanne,Mathieu, Gary,Lebel, Hélène

, p. 14203 - 14209 (2019/01/21)

The chemoselective amination of alkyl bromides and chlorides with aqueous ammonia and hydroxylamine was achieved in continuous flow to produce primary ammonium salts and hydroxylamines in high yields. An in-line workup was designed to isolate the corresponding primary amine, which was also telescoped in further reactions, such as acylation and Paal-Knorr pyrrole synthesis. Monosubstituted epoxides are also compatible with the reaction conditions.

Grinding solvent-free paal-knorr pyrrole synthesis on smectites as recyclable and green catalysts

Marvi, Omid,Nahzomi, Hossein Taherpour

, p. 139 - 147 (2018/04/23)

An environmentally benign method for the synthesis of N-substituted pyrroles from one-pot solvent-free condensation reaction of 2,5-hexanedione with various primary amines (Paal-Knorr pyrrole synthesis) on smectite clays as green and reusable heterogeneous Lewis acid catalysts is presented. The use of nontoxic, inexpensive, easily available and reusable catalysts under solvent-free conditions make this protocol practical, environmentally friendly and economically attractive.

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