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2-Ethyl-1,2-benzothiazol-3(2H)-one is a chemical compound with the molecular formula C9H7NOS. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. This particular compound features an ethyl group attached to the 2nd carbon of the benzene ring and a ketone functional group at the 3rd position of the thiazole ring. It is an organic compound that may be used in various applications, such as in the synthesis of pharmaceuticals, agrochemicals, or as a chemical intermediate. Due to its specific structure, it exhibits unique chemical properties and reactivity, making it a potentially valuable compound in the field of organic chemistry.

4299-06-3

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4299-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4299-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4299-06:
(6*4)+(5*2)+(4*9)+(3*9)+(2*0)+(1*6)=103
103 % 10 = 3
So 4299-06-3 is a valid CAS Registry Number.

4299-06-3Relevant academic research and scientific papers

151. Azidinium-Salze. 24. Mitteilung. Thermolyse heterocyclischer Azidinium-tetrafluoroborate

Huys-Francotte, Martine,Balli, Heinz

, p. 1679 - 1684 (2007/10/02)

The thermolysis of some azidinium salts was investigated.It led to a large variety of products which were isolated or identified by GC/MS.Reaction mechanisms are discussed to explain the product formation.

DISPROPORTIONIERUNGEN VON DIPHENYLDISULFIDEN ZU 1.2-BENZISOTHIAZOLEN UND o-SUBSTITUIERTEN THIOPHENOLEN UNTER ANCHIMERER BETEILIGUNG VON ORTHOSTAENDIGEN AMID-, THIOAMID- UND AMIDIN-GRUPPEN

Boeshagen, H.,Geiger, W.

, p. 325 - 330 (2007/10/02)

Substituents in the ortho position provide anchimeric support in the dissociation of diphenylsulphides.The carbamoyl group has only a weak effect.Support increases from an N,N'-disubstituted guanyl group, over thioamide to a guanyl group with an unsubstituted nitrogen atom, which effects an almost completely reversible cleavage of the disulphide group.

A Novel Route to 2-Substituted 1,2-Benzisothiazol-3(2H)-ones

Uchida, Yuzuru,Kozuka, Seizi

, p. 510 - 511 (2007/10/02)

2-Alkyl- and 2-aryl-1,2-benzisothiazol-3(2H)-ones were synthesized in high yields by the cyclization of 2-(methylsulphinyl)benzamides with thionyl chloride.

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