Welcome to LookChem.com Sign In|Join Free
  • or
2-Methoxyphenyl ethenesulfonate is an organic chemical compound with the molecular formula C8H10O4S. It is a derivative of phenyl ethenesulfonate, featuring a 2-methoxy group attached to the phenyl ring. 2-methoxyphenyl ethenesulfonate is characterized by its ability to form salts with various cations, which can be used in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its structure provides a balance of lipophilic and hydrophilic properties, which can influence its solubility and reactivity in different chemical environments. The compound is also known for its potential applications in the preparation of sulfonamide drugs, which are a class of antibiotics. Due to its reactivity and functional group diversity, 2-methoxyphenyl ethenesulfonate is a valuable intermediate in organic synthesis, particularly in the development of new chemical entities with potential therapeutic or industrial applications.

3058-68-2

Post Buying Request

3058-68-2 Suppliers

Recommended suppliers

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

3058-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3058-68-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,5 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3058-68:
(6*3)+(5*0)+(4*5)+(3*8)+(2*6)+(1*8)=82
82 % 10 = 2
So 3058-68-2 is a valid CAS Registry Number.

3058-68-2Downstream Products

3058-68-2Relevant academic research and scientific papers

Novel Bioactive Hybrid Compound Dual Targeting Estrogen Receptor and Histone Deacetylase for the Treatment of Breast Cancer

Tang, Chu,Li, Changhao,Zhang, Silong,Hu, Zhiye,Wu, Jun,Dong, Chune,Huang, Jian,Zhou, Hai-Bing

supporting information, p. 4550 - 4572 (2015/06/25)

A strategy to develop chemotherapeutic agents by combining several active groups into a single molecule as a conjugate that can modulate multiple cellular pathways may produce compounds having higher efficacy compared to that of single-target drugs. In th

Development of Selective Estrogen Receptor Modulator (SERM)-Like Activity Through an Indirect Mechanism of Estrogen Receptor Antagonism: Defining the Binding Mode of 7-Oxabicyclo[2.2.1]hept-5-ene Scaffold Core Ligands

Zheng, Yangfan,Zhu, Manghong,Srinivasan, Sathish,Nwachukwu, Jerome C.,Cavett, Valerie,Min, Jian,Carlson, Kathryn E.,Wang, Pengcheng,Dong, Chune,Katzenellenbogen, John A.,Nettles, Kendall W.,Zhou, Hai-Bing

scheme or table, p. 1094 - 1100 (2012/07/31)

Previously, we discovered estrogen receptor (ER) ligands with a novel three-dimensional oxabicyclo[2.2.1]heptene core scaffold and good ER binding affinity act as partial agonists via small alkyl ester substitutions on the bicyclic core that indirectly mo

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 3058-68-2