Welcome to LookChem.com Sign In|Join Free
  • or
C17H16Cl2N2O2S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1623809-03-9

Post Buying Request

1623809-03-9 Suppliers

Recommended suppliers

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

1623809-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1623809-03-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,3,8,0 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1623809-03:
(9*1)+(8*6)+(7*2)+(6*3)+(5*8)+(4*0)+(3*9)+(2*0)+(1*3)=159
159 % 10 = 9
So 1623809-03-9 is a valid CAS Registry Number.

1623809-03-9Downstream Products

1623809-03-9Relevant academic research and scientific papers

Photocatalytic Generation of N-Centered Hydrazonyl Radicals: A Strategy for Hydroamination of β,γ-Unsaturated Hydrazones

Hu, Xiao-Qiang,Chen, Jia-Rong,Wei, Qiang,Liu, Feng-Lei,Deng, Qiao-Hui,Beauchemin, André M.,Xiao, Wen-Jing

, p. 12163 - 12167 (2014)

A visible-light photocatalytic generation of N-centered hydrazonyl radicals has been accomplished for the first time. This approach allows efficient intramolecular addition of hydrazonyl radical to terminal alkenes, thus providing hydroamination and oxyamination products in good yields. Importantly, the protocol involves deprotonation of an N-H bond and photocatalytic oxidation to an N-centered radical, thus obviating the need to prepare photolabile amine precursors or the stoichiometric use of oxidizing reagents.

Organophotocatalytic Generation of N- and O-Centred Radicals Enables Aerobic Oxyamination and Dioxygenation of Alkenes

Hu, Xiao-Qiang,Chen, Jun,Chen, Jia-Rong,Yan, Dong-Mei,Xiao, Wen-Jing

supporting information, p. 14141 - 14146 (2016/09/23)

A cooperative TEMPO and photoredox catalytic strategy was applied for the first time to the direct conversion of N?H and O?H bonds into N- and O-centred radicals, enabling a general and selective oxidative radical oxyamination and dioxygenation of various

Efficient synthesis of dihydropyrazoles by halocyclization of β,γ-unsaturated hydrazones

Hu, Xiao-Qiang,Chen, Jia-Rong,Wei, Qiang,Liu, Feng-Lei,Deng, Qiao-Hui,Zou, You-Quan,Xiao, Wen-Jing

supporting information, p. 3082 - 3086 (2014/06/09)

An efficient halocyclization of β,γ-unsaturated hydrazones with N-bromosuccinimide was developed without the addition of any additives under mild reaction conditions to provide facile access to biologically important 4,5-dihydropyrazoles. Under the optimized conditions, a variety of highly substituted 4,5-dihydropyrazole derivatives were obtained in generally good yields. Moreover, this reaction can be further applied to the synthesis of pyrazoles in a one-pot fashion. Copyright

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 1623809-03-9