Welcome to LookChem.com Sign In|Join Free
  • or
4-Methoxybut-2-yn-1-yl 4-methylbenzenesulfonate is a chemical compound with the molecular formula C12H14O4S. It is an ester derivative of 4-methoxybut-2-yn-1-ol and 4-methylbenzenesulfonic acid. 4-methoxybut-2-yn-1-yl 4-methylbenzenesulfonate is characterized by the presence of a butyn-1-yl group with a 4-methoxy substitution, which is connected to a 4-methylbenzenesulfonate group. It is a colorless liquid with a density of 1.2 g/cm3 and a melting point of 34-36°C. The compound is soluble in organic solvents and is used in various chemical reactions and synthesis processes. Due to its reactivity, it is important to handle 4-methoxybut-2-yn-1-yl 4-methylbenzenesulfonate with care, following proper safety protocols.

209348-45-8

Post Buying Request

209348-45-8 Suppliers

Recommended suppliers

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

209348-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 209348-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,3,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209348-45:
(8*2)+(7*0)+(6*9)+(5*3)+(4*4)+(3*8)+(2*4)+(1*5)=138
138 % 10 = 8
So 209348-45-8 is a valid CAS Registry Number.

209348-45-8Downstream Products

209348-45-8Relevant academic research and scientific papers

HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF SUMO ACTIVATING ENZYME

-

Paragraph 00231, (2015/01/16)

Disclosed are compounds of formula (I): or a pharmaceutically acceptable salt thereof; wherein Y, Ra, Ra', Rc, Rf, X2, Rd, Rd', Re, Re', m, and G have the values described herein and stereochemical configurations depicted at asterisked positions indicate absolute stereochemistry, useful as inhibitors of Sumo Activating Enzyme (SAE). Further provided are pharmaceutical compositions comprising a compound of the disclosure and methods of using the compositions in the treatment of proliferative, inflammatory, cardiovascular and neurodegenerative diseases or disorders.

Fused ring aziridines as a facile entry into triazole fused tricyclic and bicyclic heterocycles

Fang, Fang,Vogel, Megan,Hines, Jennifer V.,Bergmeier, Stephen C.

scheme or table, p. 3080 - 3091 (2012/05/07)

The intramolecular dipolar cycloaddition of an azide with an alkyne has provided a useful entry into triazole fused tricyclic heterocycles containing both the triazole ring and the oxazolidin-2-one ring system. The requisite azido-alkynes have been prepared via a two-step sequence from fused ring aziridines. A series of 6-12 membered rings containing both the oxazolidinone and triazole rings have been prepared. These ring systems have been designed as conformationally restrained analogs of RNA-binding oxazolidinones. The Royal Society of Chemistry 2012.

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 209348-45-8