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943-03-3

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943-03-3 Usage

Description

2-Cyano-6-methoxybenzothiazole is an organic compound characterized by the presence of a cyano group, a methoxy group, and a benzothiazole ring. It is a versatile intermediate in the synthesis of various chemical compounds and has potential applications in different industries.

Uses

Used in Bioluminescence Applications:
2-Cyano-6-methoxybenzothiazole is used as a key intermediate in the synthesis of firefly luciferin, the light-emitting chemical responsible for the bioluminescent properties of fireflies. 2-Cyano-6-methoxybenzothiazole plays a crucial role in the development of bioluminescent systems for various applications, such as bioimaging, diagnostics, and research.
Used in Enzyme Assays:
2-Cyano-6-methoxybenzothiazole is used in the synthesis of substrates for novel ultrasensitive enzyme assays. These assays are designed to detect and measure enzyme activity with high sensitivity and specificity, which is essential for various research and diagnostic applications.
Used in Pharmaceutical Industry:
2-Cyano-6-methoxybenzothiazole is used as a reactant in the preparation of 1,2,4-Oxadiazole EthR inhibitors. These inhibitors are being developed to improve the sensitivity of the human pathogen Mycobacterium tuberculosis, which is responsible for tuberculosis, a significant global health concern.

Check Digit Verification of cas no

The CAS Registry Mumber 943-03-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 943-03:
(5*9)+(4*4)+(3*3)+(2*0)+(1*3)=73
73 % 10 = 3
So 943-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2OS/c1-12-6-2-3-7-8(4-6)13-9(5-10)11-7/h2-4H,1H3

943-03-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H51082)  6-Methoxybenzothiazole-2-carbonitrile, 99%   

  • 943-03-3

  • 1g

  • 1224.0CNY

  • Detail
  • Alfa Aesar

  • (H51082)  6-Methoxybenzothiazole-2-carbonitrile, 99%   

  • 943-03-3

  • 5g

  • 5564.0CNY

  • Detail
  • Aldrich

  • (261858)  2-Cyano-6-methoxybenzothiazole  99%

  • 943-03-3

  • 261858-1G

  • 1,331.46CNY

  • Detail

943-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Cyano-6-methoxybenzothiazole

1.2 Other means of identification

Product number -
Other names 2-CYANO-6-METHOXYBENZOTIAZOLE

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:943-03-3 SDS

943-03-3Relevant articles and documents

Rapid and scalable assembly of firefly luciferase substrates

McCutcheon, David C.,Porterfield, William B.,Prescher, Jennifer A.

supporting information, p. 2117 - 2121 (2015/03/18)

Bioluminescence imaging with luciferase-luciferin pairs is a popular method for visualizing biological processes in vivo. Unfortunately, most luciferins are difficult to access and remain prohibitively expensive for some imaging applications. Here we report cost-effective and efficient syntheses of d-luciferin and 6′-aminoluciferin, two widely used bioluminescent substrates. Our approach employs inexpensive anilines and Appel's salt to generate the luciferin cores in a single pot. Additionally, the syntheses are scalable and can provide multi-gram quantities of both substrates. The streamlined production and improved accessibility of luciferin reagents will bolster in vivo imaging efforts. This journal is

Eco-Friendly Microwave-Assisted Scaleable Synthesis of 2-Cyanobenzothiazoles via N-Arylimino-1,2,3-dithiazoles

Frere, Stephane,Thiery, Valerie,Besson, Thierry

, p. 3795 - 3804 (2007/10/03)

The cyclization procedure of N-aryl iminodithiazoles into 2-cyanobenzothiazoles was re-investigated with the aim to develop original and environmentally friendly procedures. In this article, the benefits associated with the microwave methodology are reported and the opportunity to use solvent-free procedures in order to scale up organic synthesis is studied. The result obtained show that the strong thermal effects due to graphite/microwaves interaction can be efficiently used for the synthesis of heterocyclic molecules for which traditional methods failed or are less attractive.

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