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Benzonitrile, 4-(2,5-dimethyl-1H-pyrrol-3-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138453-01-7

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138453-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138453-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,5 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138453-01:
(8*1)+(7*3)+(6*8)+(5*4)+(4*5)+(3*3)+(2*0)+(1*1)=127
127 % 10 = 7
So 138453-01-7 is a valid CAS Registry Number.

138453-01-7SDS

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 4-(2,5-dimethyl-1H-pyrrol-3-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names Benzonitrile,4-(2,5-dimethyl-1H-pyrrol-3-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:138453-01-7 SDS

138453-01-7Downstream Products

138453-01-7Relevant academic research and scientific papers

Use of Pyrrole Anions as Nucleophiles in Electrochemically Induced SRN1 Reactions

Chahma, M.,Combellas, C,Marzouk, H.,Thiebault, A.

, p. 6121 - 6124 (1991)

The reactivity of different aryl radicals towards anions of pyrroles is examined under SRN1 conditions.The coupling rate constants are determined by cyclic voltammetry.The corresponding electrolyses are performed using a redox mediator. Key Words: liquid ammonia; SRN1; electrosynthesis; substituted pyrroles.

Synthesis of 2,2,5-Trisubstituted 2 H-Pyrroles and 2,3,5-Trisubstituted 1 H-Pyrroles by Ligand-Controlled Site-Selective Dearomative C2-Arylation and Direct C3-Arylation

Yamaguchi, Miyuki,Fujiwara, Sakiko,Manabe, Kei

supporting information, p. 6972 - 6977 (2019/09/03)

Palladium-catalyzed site-selective dearomative C2-arylation of 2,5-diaryl-1H-pyrroles with aryl chlorides was accomplished, and a series of 2,2,5-triaryl-2H-pyrroles were synthesized. In addition, the site selectivity of the reaction was switched by simply changing the ligand, and the direct C3-arylated 2,3,5-triaryl-1H-pyrroles were prepared. The obtained 2,2,5-triaryl-2H-pyrroles could be further transformed into 2,2,5,5-tetraarylpyrrolidines.

SUBSTITUTED PYRROLE DERIVATIVE

-

Page/Page column 86-87, (2010/11/08)

The present invention provides a novel pyrrole derivative having excellent androgen receptor antagonism, which is represented by the formula (I): wherein R1represents a hydrogen atom, a cyano group or a group represented by the formula COORA (wherein RA represents an optional substituted C1-6 alkyl group), R2 and R4 are the same or different, and each represents a hydrogen atom, a C1-6 alkyl group, a C3-6 cycloalkyl group, a trifluoromethyl group, an amino-C1-6 alkyl group, a mono-or di-substituted amino-C1-6 alkyl group, an optionally halogenated C1-6 alkyl group substituted with an optionally substituted hydroxyl group, a C2-6 alkenyl group substituted with an optionally substituted hydroxyl group, a C1-6 alkyl group substituted with an optionally substituted and optionally oxidized thiol group, an optionally substituted with and optionally oxidized thiol group, a cyano group, an acyl group, an optionally substituted oxazolyl group or a 1,3-dioxolan-2-yl group, R3 represents a group represented by the formula (a): (wherein X represents a halogen atom, Y represents a carbon atom or a nitrogen atom, Alk represents an optionally substituted C 1-4 alkylene group, and RB represents a hydrogen atom or an acyl group), and R5 represents a phenyl group which has a cyano group at a 4-position or a 3-position thereof, and may be further substituted, or a salt thereof. The present invention also provides an androgen receptor antagonist containing the pyrrole derivative, or a salt thereof.

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