Welcome to LookChem.com Sign In|Join Free
  • or
1-(phenylsulfonyl)-2,3,4,5-tetrahydro-1H-azepine is a complex organic chemical compound with the molecular formula C11H13NO2S. It features a seven-membered azepine ring, which is partially saturated, and a phenylsulfonyl group attached to the nitrogen atom. 1-(phenylsulfonyl)-2,3,4,5-tetrahydro-1H-azepine is characterized by its unique structure, which combines the properties of both the azepine ring and the phenylsulfonyl moiety. It has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and reactivity. The compound can be synthesized through various methods, including the reaction of 1-phenylsulfonyl-1,2,3,4-tetrahydroazepine with a suitable reducing agent. Its chemical properties, such as solubility and stability, can be influenced by the presence of substituents on the phenyl ring and the azepine ring.

4750-16-7

Post Buying Request

4750-16-7 Suppliers

Recommended suppliers

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

4750-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4750-16-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4750-16:
(6*4)+(5*7)+(4*5)+(3*0)+(2*1)+(1*6)=87
87 % 10 = 7
So 4750-16-7 is a valid CAS Registry Number.

4750-16-7Relevant academic research and scientific papers

Palladium-catalysed dehydrogenative sp3 C-H bonds functionalisation into alkenes: A direct access to N-alkenylbenzenesulfonamides

Bheeter, Charles B.,Jin, Rongwei,Bera, Jitendra K.,Dixneuf, Pierre H.,Doucet, Henri

, p. 119 - 124 (2014/03/21)

The palladium-catalysed dehydrogenation of sp3 carbon-hydrogen bonds of N-alkylbenzenesulfonamides allows a simple access to N-alkenylbenzenesulfonamides. The reaction proceeds with easily accessible catalysts, with pivalate as a base, and allo

Catalytic selective oxyamidation of cyclic enamides using nitrenes

Gigant, Nicolas,Dequirez, Geoffroy,Retailleau, Pascal,Gillaizeau, Isabelle,Dauban, Philippe

, p. 90 - 94 (2012/02/16)

Yes, nitrenes did "N,O"! Intermolecular addition of nitrene to enecarbamates and enesulfonamides gives oxyamidated products in excellent yields of up to 98% and with good levels of stereoselectivity. Complete regioselectivity is also observed, leading to

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 4750-16-7