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Silane, trimethyl[1-methyl-1-(phenylsulfonyl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91787-39-2

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91787-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91787-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,8 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91787-39:
(7*9)+(6*1)+(5*7)+(4*8)+(3*7)+(2*3)+(1*9)=172
172 % 10 = 2
So 91787-39-2 is a valid CAS Registry Number.

91787-39-2Relevant academic research and scientific papers

METALATION REACTIONS. PART XVII. DILITHIATION OF PHENYL ISOPROPYL SULPHONE

Cabiddu, Maria G.,Cabiddu, Salvatore,Fattuoni, Claudia,Floris, Costantino,Gelli, Gioanna,Melis, Stefana

, p. 139 - 144 (2007/10/02)

The general utility of dimetalation reactions of phenyl iso-propyl sulphone for the preparation of ortho,alpha-substituted aryl sulphones is described.All the products were obtained in satisfactory yields. Key words: Alkyl aryl sulphones; metalation; poly

Scope and limitations in the use of α-silyl and α-stannyl sulfones as latent α-sulfonyl anions

Lamothe,Anderson,Fuchs

, p. 1675 - 1693 (2007/10/02)

Three methods for the regeneration of α-sulfonyl anions from α-silyl sulfones and α-stannyl sulfones are investigated. These methods include: (1) treatment of α-silyl sulfones with electrophiles (aldehydes and acid halides) in the presence of fluoride ion; (2) reaction of α-silyl sulfones with n-butyllithium which produces an α-silyl anion via a migration of the -SiMe3 group from the α-position to the ortho-position of the phenyl sulfones; and (3) direct transmetalation of α-stannyl sulfone by treatment with n-butyllithium. The addition of cerium [III] chloride is shown to substantially decrease enolization problems associated with addition of α-sulfonyl anions to carbonyl compounds bearing enolizable protons.

The Synthesis of Ketones via α-Silyl Sulphides

Ager, David J.

, p. 195 - 204 (2007/10/02)

α-Phenylthiosilanes (2) have been prepared by alkylation of the anion (4) derived from the 1-phenylthio-1-trimethylsilylalkane (1).These anions (4) have benn prepared by a variety of methods including, direct deprotonation of (1), displacement of a phenylthio group by lithium naphthalenide addition of an alkyl-lithium to 1-phenylthio-1-trimethylsilylethene (7), and transmetallation of a tributylstannyl moiety.The formation of an alkyl-lithium by reaction of lithium naphthalenide with a phenyl sulphide provided an additional route to (2) from bis(phenylthio)acetals (8).An alternative path to the α-phenylthiosilanes (2) was to reduce the corresponding α-phenylsulphonylsilane (15); these, in turn, being readily available from alkylation or silylation of α-sulphonyl anions.The α-phenylthiosilanes (2) were converted into the O-trimethylsilylphenylthioacetal (18) by the sila-Pummerer rearrangement, although this was complicated by vinyl sulphide (20) formation in certain cases.Subsequent hydrolysis of (18) and (20) gave the ketone (3).

Reactions of α-Silylsulphones

Ager, David J.

, p. 486 - 488 (2007/10/02)

α-Silylsulphones have been utilised to prepare vinylsulphones via the Peterson reaction and ketones by alkylation, reduction, and sila-Pummerer rearrangement.

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