1731-56-2 Usage
Description
Pyrrolidine, 1-(2,2-dimethyl-1,1-dioxido-4-phenyl-3-thietanyl)is a chemical compound that belongs to the pyrrolidine class. It features a pyrrolidine ring with a 1-(2,2-dimethyl-1,1-dioxido-4-phenyl-3-thietanyl) substituent, which contributes to its unique chemical properties and potential applications.
Uses
Used in Chemical Synthesis:
Pyrrolidine, 1-(2,2-dimethyl-1,1-dioxido-4-phenyl-3-thietanyl)is used as a building block in chemical synthesis for the creation of other organic molecules. Its unique structure allows it to be a versatile component in the development of new compounds with various applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Pyrrolidine, 1-(2,2-dimethyl-1,1-dioxido-4-phenyl-3-thietanyl)is considered a potential drug candidate for various medical conditions. Its specific properties make it a promising starting point for the development of new medications and therapies.
Safety Precautions:
It is crucial to handle Pyrrolidine, 1-(2,2-dimethyl-1,1-dioxido-4-phenyl-3-thietanyl)with care and follow established safety procedures due to the potential hazards and risks associated with its use. Proper handling minimizes the risk of adverse effects and ensures the safe application of this chemical compound in research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 1731-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,3 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1731-56:
(6*1)+(5*7)+(4*3)+(3*1)+(2*5)+(1*6)=72
72 % 10 = 2
So 1731-56-2 is a valid CAS Registry Number.
1731-56-2Relevant articles and documents
Mechanisms of Hydrolysis of (Trimethylsilyl)methanesulfonyl Chloride. Sulfene-Enamine Reactions in Water
King, James F.,Lam, Joe Y. L.
, p. 3429 - 3434 (2007/10/02)
Kinetic, product analysis, and deuteration experiments are consistent with the following mechanisms of hydrolysis of (trimethylsilyl)methanesulfonyl chloride (1) (in 0.01 M KCl at 1 deg C): (a) pH /= 10.0, attack of hydroxide anion (i) at silicon to yield sulfene (5) and (ii) at an α-hydrogen to form (trimethylsilyl)sulfene (4), in each case followed by trapping of the sulfene to give either methanesulfonate (3) or (trimethylsilyl)methanesulfonate (6) salts.Aqueous potassium fluoride catalyzes the hydrolysis of 1 with formation of the methanesulfonate 3, evidently by way of silicophilic attack of fluoride anion on 1 with formation of sulfene (5).Reaction of 1 with an enamine 7 in water (at pH 8 or 9), with or without fluoride, gives two characteristic sulfene-enamine products, (i) the four-membered cycloadduct 8 and (ii) the methylsulfonyl aldehyde 9.The same or related products are also obtained from methanesulfonyl, 2-propanesulfonyl, and phenylmethanesulfonyl chlorides and enamines in water (at pH 9).Hydrolysis of 1 is also catalyzed by aniline or triethylamine evidently giving 5.
