Welcome to LookChem.com Sign In|Join Free
  • or
o-(Phenylsulfonyl)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58844-73-8

Post Buying Request

58844-73-8 Suppliers

Recommended suppliers

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

58844-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58844-73-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,8,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58844-73:
(7*5)+(6*8)+(5*8)+(4*4)+(3*4)+(2*7)+(1*3)=168
168 % 10 = 8
So 58844-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O4S/c14-13(15)11-8-4-5-9-12(11)18(16,17)10-6-2-1-3-7-10/h1-9H,(H,14,15)

58844-73-8Relevant academic research and scientific papers

Copper(II)-catalyzed direct sulfonylation of C(sp2)-H bonds with sodium sulfinates

Rao, Wei-Hao,Shi, Bing-Feng

, p. 2784 - 2787 (2015)

A copper-catalyzed direct sulfonylation of C(sp2)-H bonds with sodium sulfinates using a removable directing group is described. This reaction tolerates a wide range of functional groups, providing an efficient protocol for the synthesis of diverse aryl sulfones. Moreover, a series of 2,6-disubstituted benzamides could be synthesized via sequential C-H functionalization.

Visible-Light Photoredox/Nickel Dual Catalysis for the Cross-Coupling of Sulfinic Acid Salts with Aryl Iodides

Liu, Nai-Wei,Hofman, Kamil,Herbert, André,Manolikakes, Georg

supporting information, p. 760 - 763 (2018/02/09)

An efficient cross-coupling of sodium or lithium sulfinates with aryl iodides, using a combination of nickel and photoredox catalysis, is described. The dual catalyst system enables a versatile synthesis of aryl sulfones at room temperature in good yields and displays a broad functional group compatibility. The potential utility of this method in the late-stage diversification of complex molecules and in the conversion of organolithium reagents and sulfur dioxide into sulfones is demonstrated.

Aromatic pyrrolidine amide prolyl endopeptidase inhibitors

-

, (2008/06/13)

A series of aromatic pyrrolidine derivatives and suitable pharmaceutically acceptable salts thereof are disclosed. These compounds are useful as PEP inhibitors in the treatment of Alzheimer's disease, amnesia, dementia, anxiety ischemia, or stroke.

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 58844-73-8