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943901-55-1

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943901-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943901-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,9,0 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943901-55:
(8*9)+(7*4)+(6*3)+(5*9)+(4*0)+(3*1)+(2*5)+(1*5)=181
181 % 10 = 1
So 943901-55-1 is a valid CAS Registry Number.

943901-55-1Relevant articles and documents

Synthesis of Allenes Bearing Phosphine Oxide Groups and Investigation of Their Reactivity toward Gold Complexes

Vanitcha, Avassaya,Gontard, Geoffrey,Vanthuyne, Nicolas,Derat, Etienne,Mouriès-Mansuy, Virginie,Fensterbank, Louis

, p. 2213 - 2218 (2015)

A collection of phosphine oxide allenes has been prepared. Their coordination to gold(I) has been studied giving new coordination complexes when a pendant pyridine moiety was present. Alternatively, their gold(I)-catalyzed cycloisomerization has proven to

Low temperature organocopper-mediated two-component cross coupling/cycloisomerization approach toward N-fused heterocycles

Chernyak, Dmitri,Gadamsetty, Surendra Babu,Gevorgyan, Vladimir

supporting information; experimental part, p. 2307 - 2310 (2009/05/11)

(Chemical Equation Presented) Organocopper reagents smoothly react with heterocyclic propargyl mesylates at low temperature to produce N-fused heterocycles. The copper reagent plays a "double duty" in this novel cascade transformation, which proceeds via an SN2′ substitution followed by a subsequent cycloisomerization step.

Lewis base-catalyzed alkynylation of carbonyl compounds with trimethylsilylacetylenes

Kitazawa, Takayuki,Minowa, Tomofumi,Mukaiyama, Teruaki

, p. 1002 - 1003 (2007/10/03)

Alkynylation of carbonyl compounds with trimethylsilylacetylenes in the presence of a catalytic amount of Lewis bases such as acetate or phenoxide anion is described. The alkynylation proceeded under mild conditions and afforded the corresponding propargyl alcohols in good to excellent yields. Copyright

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