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(2R,5S)-2-(acetoxymethyl)-5-(p-tolylthio)tetrahydrofuran-3,4-diyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

817197-67-4

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817197-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817197-67-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,1,9 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 817197-67:
(8*8)+(7*1)+(6*7)+(5*1)+(4*9)+(3*7)+(2*6)+(1*7)=194
194 % 10 = 4
So 817197-67-4 is a valid CAS Registry Number.

817197-67-4Relevant academic research and scientific papers

Synthesis of disaccharide modified berberine derivatives and their anti-diabetic investigation in zebrafish using a fluorescence-based technology

Jin, Meng,Kong, Haotian,Li, Xiaobin,Lin, Houwen,Liu, Kechun,Stoika, Rostyslav,Wang, Lizhen

, p. 3563 - 3574 (2020/05/25)

Berberine is a naturally occurring isoquinoline alkaloid and has been used as an important functional food additive in China due to its various pharmacological activities. Berberine exhibits great potential for developing anti-diabetic agents against type

InBr 3 -Catalyzed Synthesis of Aryl 1,2- trans -Thio(seleno)glycosides

Ma, Teng,Li, Changwei,Liang, Haijing,Wang, Zhaoyan,Yu, Lan,Xue, Weihua

supporting information, p. 2311 - 2314 (2017/10/06)

InBr 3 is demonstrated to be an efficient catalyst for reactions of fully acetated aldoses with aryl mercaptans or selenophenol at room temperature, rapidly furnishing the corresponding thioglycosides or selenoglycosides with exclusively 1,2- t

Stereocontrolled Total Synthesis of Muraymycin D1 Having a Dual Mode of Action against Mycobacterium tuberculosis

Mitachi, Katsuhiko,Aleiwi, Bilal A.,Schneider, Christopher M.,Siricilla, Shajila,Kurosu, Michio

supporting information, p. 12975 - 12980 (2016/10/13)

A stereocontrolled first total synthesis of muraymycin D1 (1) has been achieved. The synthetic route is highly stereoselective, featuring (1) selective β-ribosylation of the C2-methylated amino ribose, (2) selective Strecker reaction, and (3) ring-opening

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf

Kurosu, Michio,Li, Kai

supporting information; experimental part, p. 9767 - 9770 (2009/04/06)

(Chemical Equation Presented) A wide variety of p-tolyl thioriboside donors are examined for O-ribosylations of primary and secondary alcohols. p-Tolylsulfenyl trifluoromethanesulfonate (p-TolSOTf) is very effective in promoting O-ribosylations with p-tol

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