Welcome to LookChem.com Sign In|Join Free
  • or
2-Methylphenyl sulfurofluoridate, also known as 2-Methylphenyl difluoromethyl phosphate or agent 2-MP, is a chemical compound with the formula C7H6F2O2PS. It is a colorless, oily liquid that is highly toxic and can cause severe health issues upon exposure. 2-methylphenyl sulfurofluoridate is an organophosphate, which means it contains a central phosphorus atom bonded to various functional groups. 2-Methylphenyl sulfurofluoridate is a potent inhibitor of the enzyme acetylcholinesterase, leading to the accumulation of acetylcholine in the nervous system and causing overstimulation. This can result in symptoms such as muscle twitching, seizures, and respiratory failure. Due to its high toxicity and potential use in chemical warfare, it is classified as a Schedule 1 chemical weapon by the Chemical Weapons Convention.

366-39-2

Post Buying Request

366-39-2 Suppliers

Recommended suppliers

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

366-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 366-39-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 366-39:
(5*3)+(4*6)+(3*6)+(2*3)+(1*9)=72
72 % 10 = 2
So 366-39-2 is a valid CAS Registry Number.

366-39-2Relevant academic research and scientific papers

NiCl 2as a Cheap and Efficient Precatalyst for the Coupling of Aryl Fluorosulfonate and Phosphite/Phosphine Oxide

Yan, Wenjie,Zhou, Hongbo,Li, Haoyuan,Hu, Huimin,Yu, Ying,Guo, Shengmei,Cai, Hu

supporting information, p. 1453 - 1456 (2021/07/20)

Herein, NiCl 2is employed as a cheap precatalyst in the formation of C(sp 2)-P bond via cross-coupling reaction of phenol derivatives and phosphine oxides/phosphites. This catalytic system allows a variety of phenols with diverse functional groups to transform into phosphates with good yields. No additional additive is used in this reaction.

Introduction of Aryl Fluorosulfates into the Realm of Catellani Reaction Substrates

Bieliū Nas, Vidmantas,De Borggraeve, Wim M.

, p. 15706 - 15717 (2019/11/21)

Application of activated phenol fluorosulfates as substrates in a Pd/NBE mediated sequential alkylation-arylation, commonly known as a Catellani reaction, is presented. These substrates provide a level of complementarity to the commonly used aryl halides and, in combination with a plethora of existing Catellani reaction variations, enable even wider application of this powerful synthetic tool.

Nickel-catalyzed carboxylation of aryl and heteroaryl fluorosulfates using carbon dioxide

Ma, Cong,Zhao, Chuan-Qi,Xu, Xue-Tao,Li, Zhao-Ming,Wang, Xiang-Yang,Zhang, Kun,Mei, Tian-Sheng

, p. 2464 - 2467 (2019/04/10)

The development of efficient and practical methods to construct carboxylic acids using CO2 as a C1 synthon is of great importance. Nickel-catalyzed carboxylation of aryl fluorosulfates and heteroaryl fluorosulfates with CO2 is described, affording arene carboxylic acids with good to excellent yields under mild conditions. In addition, a one-pot phenol fluorosulfation/carboxylation is developed.

Aryl fluorosulfate analogues as potent antimicrobial agents: SAR, cytotoxicity and docking studies

Ravindar, Lekkala,Bukhari,Rakesh,Manukumar,Vivek,Mallesha,Xie, Zhi-Zhong,Qin, Hua-Li

, p. 107 - 118 (2018/08/21)

A series of aryl fluorosulfate analogues (1–37) were synthesized and tested for in vitro antibacterial and antifungal studies, and validated by docking studies. The compounds 9, 12, 14, 19, 25, 26, 35, 36 and 37 exhibited superior antibacterial potency ag

SO2F2-Mediated One-Pot Synthesis of Aryl Carboxylic Acids and Esters from Phenols through a Pd-Catalyzed Insertion of Carbon Monoxide

Fang, Wan-Yin,Leng, Jing,Qin, Hua-Li

supporting information, p. 2323 - 2331 (2017/09/06)

A one-pot Pd-catalyzed carbonylation of phenols into their corresponding aryl carboxylic acids and esters through the insertion of carbon monoxide has been developed. This procedure offers a direct synthesis of aryl carboxylic acids and esters from inexpensive and abundant starting materials (phenols, SO2F2 and CO) under mild conditions. This method tolerates a broad range of functional groups and is also applicable for the modification of complicated natural products.

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 366-39-2