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33143-95-2

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33143-95-2 Usage

Structure

Heterocyclic compound consisting of a benzopyran ring system with a cyanide group attached to the 6th carbon atom

Uses

Synthesis of pharmaceuticals and agrochemicals

Biological activities

Antifungal, antiviral, and antitumor properties

Aroma

Sweet, vanilla-like aroma

Enzyme inhibition

Known inhibitor of the enzyme human lactate dehydrogenase A, potential target for cancer therapy

Check Digit Verification of cas no

The CAS Registry Mumber 33143-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33143-95:
(7*3)+(6*3)+(5*1)+(4*4)+(3*3)+(2*9)+(1*5)=92
92 % 10 = 2
So 33143-95-2 is a valid CAS Registry Number.

33143-95-2Relevant articles and documents

Ph3PAuNTf2 as a superior catalyst for the selective synthesis of 2H-chromenes: Application to the concise synthesis of benzopyran natural products

Lykakis, Ioannis N.,Efe, Christina,Gryparis, Charis,Stratakis, Manolis

, p. 2334 - 2338 (2011)

Ph3PAuNTf2 (≈1 mol-%) catalyzes the selective cycloisomerization of substituted aryl propargyl ethers into 2H-chromenes in excellent yields. Benzofuran byproducts are formed only in the case of electron-deficient arenes, in up to 7% relative yield. The Ph 3PAuNTf2-catalyzed cyclization of aryl propargyl ethers was applied as a key step to the concise synthesis of the naturally occurring benzopyrans seselin, xanthyletin, precocenes I and II, 8-(3′,3′- dimethylallyl)wenteria chromene, and 2,2-dimethyl-8-prenylchromene-6-propenoic acid. Ph3PAuNTf2 is a general, highly efficient, and product-selective catalyst for the clean synthesis of 2H-chromenes from the cycloisomerization of aryl propargyl ethers.The Ph3PAuNTf 2-catalyzed cyclization was applied as a key step in the synthesis of several benzopyran-bearing naturally occurring substances. Copyright

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