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Benzoic acid, 4-methoxy-, 5-acetyl-6-benzofuranyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862823-99-2

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862823-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862823-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,8,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 862823-99:
(8*8)+(7*6)+(6*2)+(5*8)+(4*2)+(3*3)+(2*9)+(1*9)=202
202 % 10 = 2
So 862823-99-2 is a valid CAS Registry Number.

862823-99-2Downstream Products

862823-99-2Relevant academic research and scientific papers

Synthesis of benzofuran scaffold-based potential PTP-1B inhibitors

Dixit, Manish,Tripathi, Brajendra K.,Tamrakar, Akhilesh K.,Srivastava, Arvind K.,Kumar, Brijesh,Goel, Atul

, p. 727 - 734 (2007/10/03)

Protein tyrosine phosphatase 1B (PTP-1B) is an enzyme that plays a critical role in down-regulating insulin signaling through dephosphorylation of the insulin receptor. Studies have shown that PTP-1B knockout mice showed increased insulin sensitivity in m

Synthesis of functionalized acetophenones as protein tyrosine phosphatase 1B inhibitors

Dixit, Manish,Tripathi, Brajendra K.,Srivastava, Arvind K.,Goel, Atul

, p. 3394 - 3397 (2007/10/03)

Protein tyrosine phosphatase 1B (PTP1B) is an enzyme that plays a critical role in down-regulating insulin signaling through dephosphorylation of the insulin receptor. Studies have shown that PTP1B knock-out mice showed increased insulin sensitivity in mu

Amberlyst 15-catalyzed efficient synthesis of 5-acetyl-4-hydroxy-coumarone and 5-acetyl-6-hydroxy-coumarone: Crucial precursors for several naturally occurring furanoflavones

Goel, Atul,Dixit, Manish

, p. 1990 - 1994 (2007/10/03)

A novel approach to the total synthesis of naturally occurring furanoflavones and furanochalcones is described. Angular and linear furanoflavones and furanochalcones have been prepared in just four steps, using economical reagents and simple reaction cond

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