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C6H3ClN2O2S, also known as 2-Chlorobenzothiazole-7-carbothioamide or 2-Chloro-1,3-benzothiazol-7-thiol, is an organic compound with a molecular formula of C6H3ClN2O2S. It is a white to off-white crystalline powder that is sparingly soluble in water but soluble in organic solvents. C6H3ClN2O2S is commonly used in the production of pharmaceuticals, pesticides, and as an intermediate in the synthesis of various dyes and pigments. Due to its potential skin and eye irritant properties and possible harmful effects if ingested or inhaled, it is important to handle C6H3ClN2O2S with caution.

1343041-93-9

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1343041-93-9 Usage

Uses

Used in Pharmaceutical Industry:
C6H3ClN2O2S is used as an intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and reactivity in organic reactions.
Used in Pesticide Industry:
C6H3ClN2O2S is used as a key component in the formulation of pesticides, contributing to their effectiveness in controlling pests and protecting crops.
Used in Dye and Pigment Synthesis:
C6H3ClN2O2S is used as an intermediate in the synthesis of various dyes and pigments, providing a range of color options and enhancing the performance of these products in different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1343041-93-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,3,0,4 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1343041-93:
(9*1)+(8*3)+(7*4)+(6*3)+(5*0)+(4*4)+(3*1)+(2*9)+(1*3)=119
119 % 10 = 9
So 1343041-93-9 is a valid CAS Registry Number.

1343041-93-9Downstream Products

1343041-93-9Relevant academic research and scientific papers

Desulfonative Suzuki–Miyaura Coupling of Sulfonyl Fluorides

Bahadori, Maryam,Brykczyńska, Daria,Chatelain, Paul,Moran, Joseph,Muller, Cyprien,Rowley, Christopher N.,Sau, Abhijit

, p. 25307 - 25312 (2021/10/25)

Sulfonyl fluorides have emerged as powerful “click” electrophiles to access sulfonylated derivatives. Yet, they are relatively inert towards C?C bond forming transformations, notably under transition-metal catalysis. Here, we describe conditions under which aryl sulfonyl fluorides act as electrophiles for the Pd-catalyzed Suzuki–Miyaura cross-coupling. This desulfonative cross-coupling occurs selectively in the absence of base and, unusually, even in the presence of strong acids. Divergent one-step syntheses of two analogues of bioactive compounds showcase the expanded reactivity of sulfonyl fluorides to encompass both S?Nu and C?C bond formation. Mechanistic experiments and DFT calculations suggest oxidative addition occurs at the C?S bond followed by desulfonation to form a Pd-F intermediate that facilitates transmetalation.

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