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1,1-Cyclohexanedicarboxylic acid, 3,4-bis(methylene)-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94922-20-0

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94922-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94922-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,2 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94922-20:
(7*9)+(6*4)+(5*9)+(4*2)+(3*2)+(2*2)+(1*0)=150
150 % 10 = 0
So 94922-20-0 is a valid CAS Registry Number.

94922-20-0Downstream Products

94922-20-0Relevant academic research and scientific papers

PALLADIUM CATALYSED TANDEM CYCLISATION-ANION CAPTURE PROCESSES. HYDRIDE ION CAPTURE BY VINYLPALLADIUM SPECIES.

Burns, Barry,Grigg, Ronald,Sridharan, Visuvanathar,Worakun, Tanachat

, p. 4325 - 4328 (1988)

A new palladium catalysed-anion capture process is proposed.Examples are provided involving cyclisation of o-(ω-acetylenic)-aryl iodides and 2-bromo-1,6-enynes to heterocyclic- and carbocyclic-vinylpalladium species followed by hydride ion capture.

A rhodium catalyzed cycloisomerization and tandem Diels-Alder reaction for facile access to diverse bicyclic and tricyclic heterocycles

Zhou, Yirong,Nikbakht, Ali,Bauer, Felix,Breit, Bernhard

, p. 4805 - 4810 (2019/05/17)

A regioselective distal cycloisomerization of 1,6-allenenes was successfully developed to afford six-membered ring exocyclic 1,3-dienes employing a rhodium/diphosphine catalyst system. Deuterium labelling experiments and DFT calculations were performed to provide insights into the reaction mechanism of this unprecedented transformation. In addition, one-pot tandem Diels-Alder reactions with various dienophiles could readily construct diverse bicyclic and tricyclic nitrogen heterocycles, which are ubiquitous core scaffolds for a variety of natural products and bioactives. High efficiency and exclusive chemo and regioselectivities for a broad substrate scope were achieved under mild conditions using a low catalyst loading of 0.5 mol%.

RHODIUM (1) CATALYSED REGIOSPECIFIC CYCLISATION OF 1,6-ENYNES TO METHYLENECYCLOHEX-2-ENES

Grigg, Ronald,Stevenson, Paul,Worakun, Tanachat

, p. 4967 - 4972 (2007/10/02)

1,6-Enynes are cyclised regiospecifically by 5 mol percent of Wilkinson's catalyst in acetonitrile at 80 deg C to give the corresponding methylenecyclohex-2-enes usually in goog yield (62-83percent).Terminal substitution on either the alkene

REGIOSPECIFIC FORMATION OF 1,3-DIENES BY THE PALLADIUM CATALYSED INTRA- AND INTER-MOLECULAR COUPLING OF VINYL HALIDES

Grigg, Ronald,Stevenson, Paul,Worakun, Tanachat

, p. 2049 - 2054 (2007/10/02)

Palladium acetate (5 mol percent) effects catalytic inter and intra-molecular coupling of vinyl bromides in good yield under mild conditions provided sufficient triarylphosphine and potassium carbonate are present to regenerate the active palladium(0) spe

Rhodium- and Palladium-catalysed Formation of Conjugated Mono- and Bis-exocyclic Dienes. 5-Exo-Trig versus 6-Endo-Trig Cyclisations

Grigg, Ronald,Stevenson, Paul,Worakun, Tanachat

, p. 1073 - 1075 (2007/10/02)

2-Bromo-1,6-dienes are catalytically cyclised to give conjugated 5-membered bis-exocyclic dienes and 6-membered mono-exocyclic dienes by rhodium and palladium catalysts, the specificity for a 5- or 6-membered ring being a function of substrate, catalyst,

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