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Benzenesulfenyl thiocyanate, also known as phenylsulfenyl thiocyanate or phenylsulfenyl isothiocyanate, is an organic compound with the chemical formula C6H5S(=NSCN). It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. benzenesulfenyl thiocyanate is formed by the reaction of benzenesulfenyl chloride with potassium thiocyanate and is used as a reagent in organic synthesis, particularly in the preparation of various sulfur-containing compounds. Benzenesulfenyl thiocyanate is also known for its ability to act as a protecting group for thiols and as a reagent in the synthesis of sulfenamides. It is important to handle benzenesulfenyl thiocyanate with care due to its potential toxicity and reactivity.

3153-52-4

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3153-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3153-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3153-52:
(6*3)+(5*1)+(4*5)+(3*3)+(2*5)+(1*2)=64
64 % 10 = 4
So 3153-52-4 is a valid CAS Registry Number.

3153-52-4Relevant academic research and scientific papers

New Imidoyl Isothiocyanates. Chemical Behavior in Polar Solvents. Reaction with Sulfenyl Thiocyanates: Preparation of 1,2-Dihydro-2-thioxo-1,3,5-triazines and 1,3,4,6,6a-Triazadithia(6aSIV)pentalenes

Morel, Georges,Marchand, Evelyne,Haquin, Catherine,Foucaud, Andre

, p. 4043 - 4047 (2007/10/02)

The alkylthio (or arylthio) imidoyl isothiocyanates 1 can be isolated when isocyanides are treated with sulfenyl thiocyanates or via the reaction of imino chloro sulfides 3 with ammonium thiocyanate in CCl4.In a polar solvent, the dissociation of 1e-h aff

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