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Oxazole, 4,5-dihydro-4-(1-methylethyl)-2-(3,4,5-trimethoxyphenyl)-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

848477-24-7

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848477-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 848477-24-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,4,7 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 848477-24:
(8*8)+(7*4)+(6*8)+(5*4)+(4*7)+(3*7)+(2*2)+(1*4)=217
217 % 10 = 7
So 848477-24-7 is a valid CAS Registry Number.

848477-24-7Downstream Products

848477-24-7Relevant academic research and scientific papers

Cytosporone E: Racemic synthesis and preliminary antibacterial testing

Hall, Jeffrey D.,Duncan-Gould, Nathan W.,Siddiqi, Nasar A.,Kelly, Jennifer N.,Hoeferlin, L. Alexis,Morrison, Susan J.,Wyatt, Justin K.

, p. 1409 - 1413 (2005)

The antibiotic cytosporone E (isolated from the broth of the endophytic fungi CR 200 (Cytospora sp.) and CR 146 (Diaporthe sp.)) was synthesized as a racemic mixture. The key step in the synthesis is the Meyers ortho-alkylation of a chiral aromatic oxazoline. Preliminary antibiotic activity shows antibiosis against Gram-positive bacteria but not Gram-negative bacteria as previously reported.

Direct Catalytic Asymmetric Cyclopropylphosphonation Reactions of N,N-Dialkyl Groups of Aniline Derivatives by Ru(II)-Pheox Complex

Le, Chi Thi Loan,Ozaki, Seiya,Chanthamath, Soda,Shibatomi, Kazutaka,Iwasa, Seiji

, p. 4490 - 4494 (2018/08/07)

Novel catalysis involving phosphonomethylation of N-methylaniline and asymmetric cyclopropylphosphonation reactions of N,N-diethylaniline derivatives with diazomethylphosphonates are reported. Optically active cyclopropylphosphonate derivatives were directly synthesized from diazomethylphosphonates and N,N-diethylaniline derivatives catalyzed by a Ru(II)-Pheox complex in one step in good yields and high diastereoselectivities (up to trans/cis = > 99:1) and enantioselectivities (up to 99% ee). D-labeling mechanistic studies of phosphonomethylation and cyclopropylphosphonation suggested that an enamine or iminium intermediate was generated in the reaction process.

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