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3,5-bis(benzyloxy)-2-bromophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1215006-52-2

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1215006-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215006-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,5,0,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1215006-52:
(9*1)+(8*2)+(7*1)+(6*5)+(5*0)+(4*0)+(3*6)+(2*5)+(1*2)=92
92 % 10 = 2
So 1215006-52-2 is a valid CAS Registry Number.

1215006-52-2Downstream Products

1215006-52-2Relevant academic research and scientific papers

Benzofuro[3,2-d]pyrimidines inspired from cercosporamide CaPkc1 inhibitor: Synthesis and evaluation of fluconazole susceptibility restoration

Dao, Viet Hung,Ourliac-Garnier, Isabelle,Bazin, Marc-Antoine,Jacquot, Catherine,Baratte, Blandine,Ruchaud, Sandrine,Bach, Stéphane,Grovel, Olivier,Le Pape, Patrice,Marchand, Pascal

, p. 2250 - 2255 (2018)

In a context of growing resistance to classical antifungal therapy, the design of new drugs targeting alternative pathways is highly expected. Benzofuro[3,2-d]pyrimidine derivatives, derived from (?)-cercosporamide, were synthesized and evaluated as potential Candida albicans PKC inhibitors in the aim of restoring susceptibility to azole treatment. Co-administration assay of benzofuropyrimidinedione 23 and fluconazole highlighted a synergistic effect on inhibition of cell growth of a Candida albicans resistant strain.

Regioselective reactions of highly substituted arynes

Tadross, Pamela M.,Gilmore, Christopher D.,Bugga, Pradeep,Virgil, Scott C.,Stoltz, Brian M.

supporting information; experimental part, p. 1224 - 1227 (2010/06/13)

"Chemical Equation Presented" The fully regioselective reactivity of four new highly substituted silyl aryl triflate aryne precursors in aryne acyl-alkylation, acyl-alkylation/ condensation, and heteroannulation reactions is reported. The application of these more complex arynes provides access to diverse natural product scaffolds and obviates late-stage functlonallzation of aromatic rings.

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