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2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is a chemical compound characterized by a pyrrole ring with a bromine atom and a p-toluenesulfonyl group attached to it. It serves as a versatile reagent in organic synthesis, particularly for forming carbon-carbon and carbon-heteroatom bonds. Known for its unique chemical properties, 2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and biologically active molecules. It also plays a role in the development of new materials and as a building block in complex organic synthesis, making it a significant tool in medicinal chemistry research and drug discovery.

290306-56-8

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290306-56-8 Usage

Uses

Used in Pharmaceutical Industry:
2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is used as a key intermediate for the synthesis of various pharmaceuticals due to its ability to facilitate the formation of essential carbon-carbon and carbon-heteroatom bonds in drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is utilized as a reagent in the synthesis of agrochemicals, contributing to the development of new compounds with potential applications in crop protection and pest control.
Used in Medicinal Chemistry Research:
2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is employed as a research tool in medicinal chemistry, aiding in the exploration of new chemical entities and the optimization of drug candidates through its potential for diverse functionalization.
Used in Material Science:
2-BROMO-1-(P-TOLUENESULFONYL)PYRROLE 9& is also used in material science as a building block for the development of new materials, taking advantage of its unique structural and chemical features to create innovative composites and functional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 290306-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 290306-56:
(8*2)+(7*9)+(6*0)+(5*3)+(4*0)+(3*6)+(2*5)+(1*6)=128
128 % 10 = 8
So 290306-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H10BrNO2S/c1-9-4-6-10(7-5-9)16(14,15)13-8-2-3-11(13)12/h2-8H,1H3

290306-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-(4-methylphenyl)sulfonylpyrrole

1.2 Other means of identification

Product number -
Other names 2-Bromo-1-[(4-methylphenyl)sulphonyl]-1H-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:290306-56-8 SDS

290306-56-8Relevant academic research and scientific papers

S2 emission from chemically modified BODIPYs

Cho, Dae Won,Fujitsuka, Mamoru,Ryu, Jung Ho,Lee, Myoung Hee,Kim, Hwan Kyu,Majima, Tetsuro,Im, Chan

supporting information; experimental part, p. 3424 - 3426 (2012/05/20)

Novel boron dipyrromethene (BODIPY) derivatives having significant absorption and emission in the longer wavelength region were synthesized. BODIPY showed anomalous S2 emission from the second excited (S2) state at shorter wavelength

2-Bromo-N-(p-toluenesulfonyl)pyrrole: A Robust Derivative of 2-Bromopyrrole

Knight, Lea W.,Huffman, John W.,Isherwood, Matthew L.

, p. 1993 - 1996 (2007/10/03)

2-Bromo-AL(p-toluenesulfonyl)pyrrole (2), a crystalline stable derivative of 2-bromopyrrole (1) has been prepared in 80% yield by bromination of pyrrole, followed by conversion to the N-(p-toluenesulfonyl) derivative. This compound is stable indefinitely at ambient temperature. Compound 2 is an excellent substrate for Suzuki coupling with arylboronic acids.

Condensation reactions of a nitrodienamine with organocopper and alkyllithium reagents prepared from pyrrole derivatives

Koike, Takeshi,Shinohara, Yoshifumi,Nishimura, Takeshi,Hagiwara, Masanori,Tobinaga, Seisho,Takeuchi, Naoki

, p. 1351 - 1359 (2007/10/03)

Condensation reactions of a nitrodienamine (1) with Grignard, organocopper and alkyllithium reagents prepared from pyrrole derivatives were investigated.

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