Welcome to LookChem.com Sign In|Join Free

CAS

  • or

87840-72-0

Post Buying Request

87840-72-0 Suppliers

Recommended suppliersmore

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

87840-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87840-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87840-72:
(7*8)+(6*7)+(5*8)+(4*4)+(3*0)+(2*7)+(1*2)=170
170 % 10 = 0
So 87840-72-0 is a valid CAS Registry Number.

87840-72-0Relevant articles and documents

TRIAZINONE COMPOUNDS

-

Paragraph 1263; 1264, (2014/08/06)

The invention provides a compound of Formula (I) pharmaceutically acceptable salts, pro-drugs, biologically active metabolites, stereoisomers and isomers thereof wherein the variable are defined herein. The compounds of the invention are useful for treati

Bimetallic catalysis involving dipalladium(I) and diruthenium(I) complexes

Das, Raj K.,Saha, Biswajit,Rahaman, S. M. Wahidur,Bera, Jitendra K.

scheme or table, p. 14459 - 14468 (2011/03/19)

Dipalladium(I) and diruthenium(I) compounds bridged by two [{(5,7-dimethyl-1,8-naphthyridin-2-yl)amino}carbonyl]ferrocene (L) ligands have been synthesized. The X-ray structures of [Pd2L2][BF 4]2 (1) and [Ru2L2(CO) 4][BF4]2 (2) reveal dinuclear structures with short metal-metal distances. In both of these structures, naphthyridine bridges the dimetal unit, and the site trans to the metal-metal bond is occupied by weakly coordinating oxygen from the amido fragment. The catalytic utilities of these bimetallic compounds are evaluated. Compound 1 is an excellent catalyst for phosphine-free, Suzuki cross-coupling reactions of aryl bromides with arylboronic acids and provides high yields in short reaction times. Compound 1 is also found to be catalytically active for aryl chlorides, although the corresponding yields are lower. A bimetallic mechanism is proposed, which involves the oxidative addition of aryl bromide across the Pdi£ Pd bond and the bimetallic reductive elimination of the product. Compound 1 is also an efficient catalyst for the Heck cross-coupling of aryl bromides with styrenes. The mechanism for aldehyde olefination with ethyl diazoacetate (EDA) and PPh3, catalyzed by 2, has been fully elucidated. It is demonstrated that 2 catalyzes the formation of phosphorane utilizing EDA and PPh3, which subsequently reacts with aldehyde to produce a new olefin and phosphine oxide. The efficacy of bimetallic complexes in catalytic organic transformations is illustrated in this work. Good couple: Metal-metal singly bonded [PdIi£PdI] and [RuIi£RuI] complexes exhibit bimetallic synergy in the catalytic Ci£C bond-coupling and aldehyde-olefination reactions, respectively (see figure). Copyright

Osmium-catalyzed olefin dihydroxylation and aminohydroxylation in the second catalytic cycle

Wu, Peng,Hilgraf, Robert,Fokin, Valery V.

, p. 1079 - 1085 (2007/10/03)

Two catalytic cycles operate in the osmium-catalyzed olefin dihydroxylation and aminohydroxylation. Slow hydrolysis of the Os(VI) monoglycolate (or monoazaglycolate in aminohydroxylation) intermediate often results in the addition of another molecule of o

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 87840-72-0