Welcome to LookChem.com Sign In|Join Free
  • or
(2R,3R)-3-Hydroxy-2,4,4-trimethyl-pentanethioic acid S-tert-butyl ester is a complex organic compound with the molecular formula C12H24O2S. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific 2R,3R configuration. (2R,3R)-3-Hydroxy-2,4,4-trimethyl-pentanethioic acid S-tert-butyl ester features a hydroxyl group, a thiol group, and a tert-butyl ester group, which contribute to its unique chemical properties. The hydroxyl group is attached to the third carbon, while the thiol group is part of the pentanethioic acid backbone. The tert-butyl ester group is a bulky, sterically hindered group that protects the thiol functionality. (2R,3R)-3-Hydroxy-2,4,4-trimethyl-pentanethioic acid S-tert-butyl ester is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals or other specialty chemicals due to its unique structural features and reactivity.

97250-90-3

Post Buying Request

97250-90-3 Suppliers

Recommended suppliers

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

97250-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97250-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,5 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97250-90:
(7*9)+(6*7)+(5*2)+(4*5)+(3*0)+(2*9)+(1*0)=153
153 % 10 = 3
So 97250-90-3 is a valid CAS Registry Number.

97250-90-3Downstream Products

97250-90-3Relevant academic research and scientific papers

A CONVENIENT METHOD FOR GENERATION OF TIN(II) THIOESTER ENOLATE AND ITS REACTION WITH ALDEHYDE

Mukaiyama, Teruaki,Yamasaki, Noritsugu,Stevens, Rodney W.,Murakami, Masahiro

, p. 213 - 216 (2007/10/02)

Tin(II) enolates of thioesters are conveniently generated by the addition of stannous thiolates to ketenes.The tin(II) enolates thus formed react with aldehydes to afford the corresponding β-hydroxythioesters in a syn-selective manner.And this method is applied to an enantioselective formation of β-hydroxythioesters by the use of a chiral diamine as ligand.

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 97250-90-3