Welcome to LookChem.com Sign In|Join Free
  • or
N-(1,2-dicarba-closo-dodecaboran-9-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1254975-69-3

Post Buying Request

1254975-69-3 Suppliers

Recommended suppliers

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

1254975-69-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1254975-69-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,4,9,7 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1254975-69:
(9*1)+(8*2)+(7*5)+(6*4)+(5*9)+(4*7)+(3*5)+(2*6)+(1*9)=193
193 % 10 = 3
So 1254975-69-3 is a valid CAS Registry Number.

1254975-69-3Downstream Products

1254975-69-3Relevant academic research and scientific papers

Catalytic Oxidative Dehydrogenative Coupling of Cage B-H/B-H Bonds for Synthesis of Bis(o-carborane)s

Wu, Ji,Cao, Ke,Zhang, Cai-Yan,Xu, Tao-Tao,Ding, Li-Fang,Li, Bo,Yang, Junxiao

, p. 5986 - 5989 (2019)

An efficient and succinct protocol for synthesis of bis(o-carborane) connected by a B-B bond via palladium catalyzed oxidative dehydrogenative coupling of cage B-H/B-H bonds was developed for the first time. A series of bis(o-carborane)s connected by B(4)

Palladium catalyzed/counter ion tuned selective methylation of o-carboranes

Cao, Ke,Zhang, Cai-Yan,Xu, Tao-Tao,Wu, Ji,Ding, Li-Fang,Jiang, Linhai,Yang, Junxiao

, (2019)

The palladium catalyzed/counter ion tuned selective methylation of 9-amide-o-carboranes on B(4) and B(12) has been developed, and a series of o-carborane derivatives decorated with various groups have been synthesized with moderate yields. The in situ for

A facile approach for the synthesis of nido-carborane fused oxazoles via one pot deboronation/cyclization of 9-amide-o-carboranes

Zhang, Cai-Yan,Cao, Ke,Xu, Tao-Tao,Wu, Ji,Jiang, Linhai,Yang, Junxiao

, p. 830 - 833 (2019)

A one pot deboronation/cyclization of 9-amide-o-carboranes for the synthesis of nido-7,8-carborane fused oxazole by cooperation of Pd(OAc)2, AgOAc and K2CO3 has been developed. A plausible mechanism involving an amide dire

Palladium catalyzed selective arylation of: O -carboranes via B(4)-H activation: Amide induced regioselectivity reversal

Xu, Tao-Tao,Cao, Ke,Zhang, Cai-Yan,Wu, Ji,Jiang, Linhai,Yang, Junxiao

, p. 13603 - 13606 (2018)

By changing the charge distribution of boron vertices via introducing an amide on cage B(9), the selective B(4) arylation of o-carboranes via Suzuki-Miyaura coupling has been developed. A series of o-carborane derivatives decorated with diverse active groups have been synthesized with moderate to good yields, which have been proved to be further transformed to a novel kind of tri-substituted nido-carborane fused oxazole with potential application in boron neutron capture therapy, organometallic as well as coordination chemistry.

Novel approach to aminocarboranes by mild amidation of selected iodo-carboranes

Sevryugina, Yulia,Julius, Richard L.,Hawthorne, M. Frederick

, p. 10627 - 10634 (2011/02/18)

A mild protocol for the palladium-catalyzed Buchwald-Hartwig amidation of icosahedral carboranes is described. Employing 2-dicyclohexylphosphino-2′- (N,N-dimethylamino)biphenyl (1) as a ligand and K3PO4as a base, benzamide, trifluoro

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 1254975-69-3