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2,2,4,4-Tetramethyl-3-phenylsulfonylpentane is an organic compound with the molecular formula C19H30O2S. It is a colorless liquid with a molecular weight of 318.51 g/mol. 2,2,4,4-tetramethyl-3-phenylsulfonylpentane is characterized by its unique structure, which includes a pentane backbone with four methyl groups (CH3) at the 2nd and 4th carbon positions, and a phenylsulfonyl group (C6H5-SO2-) attached to the 3rd carbon. The phenylsulfonyl group is a functional group derived from benzene, with a sulfonyl group (-SO2-) attached to it. 2,2,4,4-tetramethyl-3-phenylsulfonylpentane is primarily used in chemical research and as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its complex structure, it is not commonly found in nature and is typically synthesized in a laboratory setting.

58712-14-4

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58712-14-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58712-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,1 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 58712-14:
(7*5)+(6*8)+(5*7)+(4*1)+(3*2)+(2*1)+(1*4)=134
134 % 10 = 4
So 58712-14-4 is a valid CAS Registry Number.

58712-14-4Downstream Products

58712-14-4Relevant academic research and scientific papers

α-arylsulfanyl-α-fluoro carbenoids: Their novel chemistry and synthetic applications

Pohmakotr, Manat,Ieawsuwan, Winai,Tuchinda, Patoomratana,Kongsaeree, Palangpon,Prabpai, Samran,Reutrakul, Vichai

, p. 4547 - 4550 (2007/10/03)

(Chemical equation presented) The bromine-magnesium exchange reactions of arylthiobromodifluoromethanes with Grignard reagents have been studied. Upon trapping with electrophiles, alkyl aryl sulfides and ketenedithioacetals are obtained. The reaction is p

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