Welcome to LookChem.com Sign In|Join Free
  • or
hexyl p-toluenesulfinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74698-01-4

Post Buying Request

74698-01-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

74698-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74698-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74698-01:
(7*7)+(6*4)+(5*6)+(4*9)+(3*8)+(2*0)+(1*1)=164
164 % 10 = 4
So 74698-01-4 is a valid CAS Registry Number.

74698-01-4Downstream Products

74698-01-4Relevant academic research and scientific papers

One-pot three-component sulfone synthesis exploiting palladium-catalysed aryl halide aminosulfonylation

Richards-Taylor, Charlotte S.,Blakemore, David C.,Willis, Michael C.

, p. 222 - 228 (2014/01/06)

A palladium-catalysed aminosulfonylation process is used as the key-step in a one-pot, three-component sulfone synthesis. The process combines aryl-, heteroaryl- and alkenyl iodides with a sulfonyl unit and an electrophilic coupling fragment. The sulfonyl unit is delivered in the form of an aminosulfonamide, which then serves as a masked sulfinate. The sulfinate is combined, in situ, with an electrophilic coupling partner, such as a benzylic, allylic or alkyl halide, an electron-poor arene, or a cyclic epoxide, to provide the corresponding sulfone products in good to excellent yields. The mild reaction conditions and use of commercially available reaction components allows the easy preparation of a broad range of sulfones featuring a variety of functional groups. The process obviates the need to employ thiol starting materials, and oxidative operations.

SYNTHESIS OF dl-PENTALENOLACTONES E AND F.

Cane,Thomas

, p. 5295 - 5303 (2007/10/12)

The methyl esters of ( plus or minus )-pentalenolactone E and F have been synthesized by a route based on the intramolecular insertion of an alpha -acylcarbene into an unactivated C-H bond to effect closure of the key fused delta -lactone ring system. Lactone reduction, deketalization, and selective acetalization of the derived lactol provided as a mixture of epimers.

Novel One-Step Preparation of Sulfinic Acid Derivatives from Sulfinic Acid

Furukawa, Mitsuru,Ohkawara, Tadashi,Noguchi, Yoshihide,Nishikawa, Masumi,Tomimatsu, Masahide

, p. 134 - 141 (2007/10/02)

Convenient one-step syntheses of sulfinamides and sulfinate esters from sulfinic acids were achieved by using coupling reagents, such as 2-chloro-1-methylpyridinium iodide, γ-saccharine chloride, N,N'-dicyclohexylcarbodiimide, and diethyl azodicarboxylate and triphenylphosphine.Ammonolysis of sulfinate esters also give sulfinamides.Keyword- sulfinic acid; sulfinamide; sulfinate ester; sulfinyl-transfer reagent; coupling reaction; 2-chloro-1-methylpyridinium iodide; γ-saccharine chloride; N,N'-dicyclohexylcarbodiimide; diethyl azodicarboxylate; triphenylphosphine

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 74698-01-4