Welcome to LookChem.com Sign In|Join Free
  • or
Propanoic acid, 3-[[4-(1,1-dimethylethyl)phenyl]thio]-, also known as 3-(4-tert-butylphenylthio)propanoic acid, is an organic compound with the chemical formula C13H18O2S. It is a derivative of propanoic acid, featuring a tert-butyl group attached to the phenyl ring and a thiol group (-SH) connected to the phenyl ring as well. Propanoic acid, 3-[[4-(1,1-dimethylethyl)phenyl]thio]- is characterized by its molecular weight of 242.35 g/mol and a melting point of 47-49°C. It is a colorless to pale yellow solid and is soluble in organic solvents. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of fungicides and herbicides. Due to its potential applications in the chemical industry, it is essential to handle Propanoic acid, 3-[[4-(1,1-dimethylethyl)phenyl]thio]- with care, as it may have adverse effects on the environment and human health if not properly managed.

6612-45-9

Post Buying Request

6612-45-9 Suppliers

Recommended suppliers

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

6612-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6612-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,1 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6612-45:
(6*6)+(5*6)+(4*1)+(3*2)+(2*4)+(1*5)=89
89 % 10 = 9
So 6612-45-9 is a valid CAS Registry Number.

6612-45-9Downstream Products

6612-45-9Relevant academic research and scientific papers

Development of conjugate addition of lithium dialkylcuprates to thiochromones: Synthesis of 2-alkylthiochroman-4-ones and additional synthetic applications

Bass, Shekinah A.,Parker, Dynasty M.,Bellinger, Tania J.,Eaton, Aireal S.,Dibble, Angelica S.,Koroma, Kaata L.,Sekyi, Sylvia A.,Pollard, David A.,Guo, Fenghai

, (2018)

Lithium dialkylcuprates undergo conjugate addition to thiochromones to afford 2-alkylthiochroman-4-ones in good yields. This approach provide an efficient and general synthetic approach to privileged sulfur-containing structural motifs and valuable precursors for many pharmaceuticals, starting from common substrates-thiochromones. Good yields of 2-alkyl-substituted thiochroman-4-ones are attained with lithium dialkylcuprates, lithium alkylcyanocuprates or substoichiometric amount of copper salts. The use of commercially available inexpensive alkyllithium reagents will expedite the synthesis of a large library of 2-alkyl substituted thiochroman-4-ones for additional synthetic applications.

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 6612-45-9