1115-06-6 Usage
General Description
The chemical compound (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane, with the formula C6H15NOS3, is a thioxomethane derivative containing nitrogen, oxygen, sulfur, and carbon atoms. It is also known as dimethylthioxamoyl dimethyldisulfide and is used as a reagent in organic synthesis. (dimethylamino)[(dimethylcarbamoyl)disulfanyl]thioxomethane is a white to off-white powder with a molecular weight of 225.32 g/mol. It is used in pharmaceuticals and agrochemicals, and it is also an important intermediate in chemical reactions. Additionally, it has potential applications in the fields of medicine and agriculture due to its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1115-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1115-06:
(6*1)+(5*1)+(4*1)+(3*5)+(2*0)+(1*6)=36
36 % 10 = 6
So 1115-06-6 is a valid CAS Registry Number.
1115-06-6Relevant articles and documents
THE REACTION OF t-BUTYL HYPOCHLORITE WITH THIOCARBONYL COMPOUND - A CONVENIENT METHOD FOR THE TRANSFORMATION
El-Wassimy, M.T.M.,Jorgensen, K.A.,Lawesson, S.-O.
, p. 1729 - 1734 (2007/10/02)
The reaction of t-butyl hypochlorite with different thiocarbonyl compounds has been studied.Primary thioamides 1a-c give 1,2,4-thiadiazole derivatives.N-Phenylthiourea 4a gives 5-imino-4-phenyl-3-phenylamino-4,5-dihydro-1,2,4-thiadiazoline 15.Secondary and tertiary thioamides 2a-d, N-methyl-2-thiopyrrolidinone 3, N,N'-dicyclohexylthiourea 4b, N,N,N'-trimethylthiourea 4c, 5-ethyl-5-phenylthiobarbituric acid 5, xanthione 7a, Mischler's thioketone 7b, thiocoumarin 8, O-ethylthiobenzoate 9, O,O-diphenylthiocarbonate 10, di-p-tolyl and o-phenylene trithiocarbonates 11 and 12 have all afforded the oxigen analogues.N,N-Dimethyl-S-phenyldithiocarbonate 6 produces a mixture of di-, tri-, and tetrasulfides.A mechanism for the transformation is suggested in accordance with the Hard and Soft Acids and Bases (HSAB) principle.
