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91026-00-5

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91026-00-5 Usage

Description

N-BENZYL-2 3-DIBROMOMALEIMIDE 97 is a chemical compound that serves as a key intermediate in the synthesis of various maleimide-based dyes. These dyes are known for their fluorescence quenching properties, making them valuable in research and analytical applications.

Uses

Used in Fluorescence Quenching Applications:
N-BENZYL-2 3-DIBROMOMALEIMIDE 97 is used as a precursor in the synthesis of maleimide-based dyes for fluorescence quenching. These dyes are employed in various research and analytical applications, where they can effectively suppress fluorescence signals, allowing for more accurate measurements and analyses.
Used in Synthesis of Maleimide-based Dyes:
N-BENZYL-2 3-DIBROMOMALEIMIDE 97 is used as a starting material in the synthesis of several maleimide-based dyes, including:
1. 2,3-bis(3-indolyl)-N-benzylmaleimide
2. 2,3-bis(2′-methyl-3-indolyl)-N-benzylmaleimide
3. 2,3-bis(2-pyrrolyl)-N-benzylmaleimide
4. 2-aryl-N-benzyl-3-bromomaleimides via Suzuki cross-coupling reaction with aryl boronic acid
These dyes are specifically designed for fluorescence quenching, making them useful in a variety of scientific and industrial applications where the suppression of fluorescence is required.

Check Digit Verification of cas no

The CAS Registry Mumber 91026-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,2 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91026-00:
(7*9)+(6*1)+(5*0)+(4*2)+(3*6)+(2*0)+(1*0)=95
95 % 10 = 5
So 91026-00-5 is a valid CAS Registry Number.

91026-00-5 Well-known Company Product Price

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  • Aldrich

  • (557781)  N-Benzyl-2,3-dibromomaleimide  97%

  • 91026-00-5

  • 557781-5G

  • 4,531.41CNY

  • Detail

91026-00-5SDS

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 1-benzyl-3,4-dibromopyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 1-benzyl-3,4-dibromopyrole-2,5-dione

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:91026-00-5 SDS

91026-00-5Relevant articles and documents

Electrochemical synthesis method of 3,4-dibromomalayimide

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Paragraph 0072-0076; 0103-0104; 0106-0107; 0109-0110; ..., (2022/01/10)

The present invention relates to the field of organic synthesis technology, in particular to a 3,4-dibromo maleimide electrochemical synthesis method, maleimide as the starting material, to inexpensive, safe and readily available bromide as a bromine sour

Discovery of new effective N-alkyl-3,4-diarylmaleimides-based drugs for reversing the bacterial resistance to rhodamine 6G in Bacillus subtilis

Mendoza-Macías, Claudia Leticia,Solorio-Alvarado, Cesar Rogelio,Alonso-Castro, Angel Josabad,Alba-Betancourt, Clara,Deveze-álvarez, Martha Alicia,Padilla-Vaca, Felipe,Reyes-Gualito, Arturo

, p. 1429 - 1438 (2019/11/28)

Multidrug resistance (MDR) is a great concern worldwide. There is a great need to develop new drugs with the potential to attack target cells that show MDR phenotype. The purpose of this study was to assess the reversing effect of new N-alkyl-3,4-diarylma

Maleimide-based acyclic enediyne for efficient DNA-cleavage and tumor cell suppression

Song, Depeng,Sun, Shiyuan,Tian, Yu,Huang, Shuai,Ding, Yun,Yuan, Yuan,Hu, Aiguo

supporting information, p. 3195 - 3200 (2015/04/27)

A pH-sensitive acyclic enediyne (1) was synthesized for efficient DNA-cleavage and tumor cell suppression. Unlike other acyclic enediynes, this novel enediyne transforms into a highly reactive enediyne (2) in an acidic environment only, which undergoes Be

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