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2-Amino-4-chlorothiobenzaMide, 97%, is a high-purity chemical compound with the molecular formula C7H6ClNS. It is a white crystalline solid that is widely used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. 2-AMino-4-chlorothiobenzaMide, 97% is characterized by its unique structure, which includes an amino group, a chloro group, and a thioamide group, making it a versatile building block for various chemical reactions. The 97% purity indicates that the product is of high quality, with minimal impurities, which is crucial for applications requiring precise chemical properties.

2586-93-8

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2586-93-8 Usage

Chemical compound

2-Amino-4-chlorothiobenzamide

Purity

97%

Appearance

White to off-white solid

Primary use

Pharmaceutical and chemical industries

Common use

Intermediate in synthesis of pharmaceuticals and agrochemicals

Additional use

Research and development for new drugs and chemical compounds

Applications

Reacts with other compounds, unique chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 2586-93-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2586-93:
(6*2)+(5*5)+(4*8)+(3*6)+(2*9)+(1*3)=108
108 % 10 = 8
So 2586-93-8 is a valid CAS Registry Number.

2586-93-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H52249)  2-Amino-4-chlorothiobenzamide, 97%   

  • 2586-93-8

  • 1g

  • 1029.0CNY

  • Detail
  • Alfa Aesar

  • (H52249)  2-Amino-4-chlorothiobenzamide, 97%   

  • 2586-93-8

  • 5g

  • 4136.0CNY

  • Detail

2586-93-8Downstream Products

2586-93-8Relevant academic research and scientific papers

Catalyst-free synthesis of 2-aryl-1,2-dihydro-quinazolin-4(1H)-thiones from 2-aminobenzothio-amides and aldehydes in water

Oschatz, Stefan,Brunzel, Tom,Wu, Xiao-Feng,Langer, Peter

, p. 1150 - 1158 (2015/08/03)

2-Dihydroquinazolin-4(1H)-thiones were prepared in up to excellent yields from 2-aminobenzothioamides and aldehydes. The reaction is carried out in water without the use of any catalyst or promoter. The sulfur-containing substrate can be obtained easily by thiation of the corresponding nitrile by solid sodium hydrosulfide.

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