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66904-34-5

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66904-34-5 Usage

Thiazole derivative

A benzothiazole-based compound This refers to the structure of the compound, which is derived from a 1,3-thiazole ring, a five-membered ring system containing sulfur and nitrogen atoms.

Nitro group

At the 6-position A nitro group (-NO2) is attached to the sixth position of the benzothiazole ring, which influences the compound's reactivity and potential applications.

Intermediate in synthesis

Used in pharmaceuticals and agrochemicals The compound serves as a building block or intermediate in the synthesis of various pharmaceutical and agrochemical products, making it valuable in these industries.

Potential antifungal and antibacterial properties

Studied for its bioactivity Research has explored the potential of 2-(butylsulfanyl)-6-nitro-1,3-benzothiazole to exhibit antifungal and antibacterial properties, which could lead to its use in treatments or applications.

Precursor for heterocyclic compounds

Nitro group's reactivity The presence of the nitro group makes the compound a useful precursor for the synthesis of various heterocyclic compounds, as it can be easily modified or transformed in chemical reactions.

Versatile chemical

Application in diverse fields Due to its unique structure and properties, 2-(butylsulfanyl)-6-nitro-1,3-benzothiazole finds application in various fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 66904-34-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,0 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66904-34:
(7*6)+(6*6)+(5*9)+(4*0)+(3*4)+(2*3)+(1*4)=145
145 % 10 = 5
So 66904-34-5 is a valid CAS Registry Number.

66904-34-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butylsulfanyl-6-nitro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names Benzothiazole,2-(butylthio)-6-nitro

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:66904-34-5 SDS

66904-34-5Downstream Products

66904-34-5Relevant articles and documents

Lewis acid-catalyzed, copper(II)-mediated synthesis of heteroaryl thioethers under base-free conditions

Dai, Chao,Xu, Zhaoqing,Huang, Fei,Yu, Zhengkun,Gao, Yan-Feng

experimental part, p. 4414 - 4419 (2012/06/18)

A Lewis acid (AgI, NiII, or FeII) catalyzed, CuII-mediated thiolation reaction between heteroarenes and thiols was achieved with good yield under base-free conditions. DMSO could serve as an effective methylthiolation reagent for the synthesis of heterocyclic methyl thioethers.

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