Welcome to LookChem.com Sign In|Join Free

CAS

  • or

168213-35-2

Post Buying Request

168213-35-2 Suppliers

Recommended suppliersmore

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

168213-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168213-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,2,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 168213-35:
(8*1)+(7*6)+(6*8)+(5*2)+(4*1)+(3*3)+(2*3)+(1*5)=132
132 % 10 = 2
So 168213-35-2 is a valid CAS Registry Number.

168213-35-2Relevant articles and documents

Iridium-Catalyzed Distal Hydroboration of Aliphatic Internal Alkenes

Wang, Guangzhu,Liang, Xinyi,Chen, Lili,Gao, Qian,Wang, Jian-Guo,Zhang, Panke,Peng, Qian,Xu, Senmiao

supporting information, p. 8187 - 8191 (2019/05/27)

The regioselective hydroboration of aliphatic internal alkenes remains a great challenge. Reported herein is an iridium-catalyzed hydroboration of aliphatic internal alkenes, providing distal-borylated products in good to excellent yields with high regioselectivity (up to 99:1). We also demonstrate that the C?B bond of the distal-borylated product can be readily converted into other functional groups. DFT calculations indicate that the reaction proceeds through an unexpected IrIII/IrV cycle.

Chiral Selenide-Catalyzed Enantioselective Construction of Saturated Trifluoromethylthiolated Azaheterocycles

Luo, Jie,Liu, Yannan,Zhao, Xiaodan

supporting information, p. 3434 - 3437 (2017/07/15)

An indane-based, bifunctional, chiral selenide catalyst has been developed. The new catalyst is efficient for the enantioselective synthesis of saturated azaheterocycles possessing a trifluoromethylthio group. The desired products were obtained in good yields with high diastereo- and enantioselectivities.

Efficient amide-directed catalytic asymmetric hydroboration

Smith, Sean M.,Thacker, Nathan C.,Takacs, James M.

, p. 3734 - 3735 (2008/09/20)

A series of acyclic β,γ-unsaturated amides are shown to undergo highly regio- (>95%) and enantioselective (93-99% ee) rhodium-catalyzed hydroboration with pinacolborane (PinBH) using simple chiral monophosphite or phosphoramidite ligands in combination wi

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

What can I do for you?
Get Best Price

Get Best Price for 168213-35-2