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Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI), also known as 6-nitrobenzothiazol-2-yl methyl ketone, is a chemical compound with the molecular formula C9H6N2O3S. It is a yellow crystalline solid that is commonly used in research and development as a fluorescent labeling reagent for proteins and peptides. Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI) has been studied for its potential applications in the fields of biochemistry and pharmaceuticals, particularly in fluorescent imaging and labeling techniques. It is also known for its ability to selectively bind to specific proteins and can be used as a probe in various biological studies. However, it is important to handle this chemical with care, as it may pose health risks if not used properly.

94834-02-3

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94834-02-3 Usage

Uses

Used in Biochemistry Research:
Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI) is used as a fluorescent labeling reagent for proteins and peptides, enabling researchers to track and visualize their behavior in biological systems.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI) is utilized for its potential applications in fluorescent imaging and labeling techniques, which can aid in the development of new drugs and therapies.
Used in Fluorescent Imaging Techniques:
Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI) is employed as a fluorescent probe in various biological studies, allowing for the selective binding to specific proteins and facilitating the investigation of their functions and interactions within complex biological systems.
Used in Protein Interaction Studies:
Due to its ability to selectively bind to proteins, Ethanone, 1-(6-nitro-2-benzothiazolyl)(9CI) is used in studies aimed at understanding protein-protein interactions, which can provide insights into the mechanisms of various diseases and potential therapeutic targets.

Check Digit Verification of cas no

The CAS Registry Mumber 94834-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,3 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94834-02:
(7*9)+(6*4)+(5*8)+(4*3)+(3*4)+(2*0)+(1*2)=153
153 % 10 = 3
So 94834-02-3 is a valid CAS Registry Number.

94834-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-nitro-1,3-benzothiazol-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names -

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:94834-02-3 SDS

94834-02-3Downstream Products

94834-02-3Relevant academic research and scientific papers

Peroxides as "switches" of dialkyl H-phosphonate: Two mild and metal-free methods for preparation of 2-acylbenzothiazoles and dialkyl benzothiazol-2-ylphosphonates

Chen, Xiao-Lan,Li, Xu,Qu, Ling-Bo,Tang, Yu-Chun,Mai, Wen-Peng,Wei, Dong-Hui,Bi, Wen-Zhu,Duan, Li-Kun,Sun, Kai,Chen, Jian-Yu,Ke, Dian-Dian,Zhao, Yu-Fen

, p. 8407 - 8416 (2015/03/18)

Two mild and metal-free methods for the preparation of two kinds of important benzothiazole derivatives, 2-acylbenzothiazoles and dialkyl benzothiazol-2-ylphosphonates, respectively, were developed. The dialkyl H-phosphonate (RO)2P(O)H exists i

1,3-vs- 1,5-DIPOLAR REACTIVITY OF 1-PHENYLMETHYL-4N-ACETYLIMINO-1H-1,2,4-TRIAZOLIUM BETAIN TOWARD AROMATIC ISOTHIOCYANATES

Zalupsky, Peter,Martvon, Augustin

, p. 1713 - 1721 (2007/10/02)

The title betain I was found to display both 1,3- and 1,5-dipolar reactivity, depending on reaction conditions.Whereas the reaction with aromatic isothiocyanates in nonpolar solvents produced cycloadducts in concerted manner stepwise addition in dimethylf

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