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tricalysionol A 9-O-(S)-α-methoxy-α-trifluoromethylphenylacetic acid ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1309362-84-2

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1309362-84-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309362-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,3,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1309362-84:
(9*1)+(8*3)+(7*0)+(6*9)+(5*3)+(4*6)+(3*2)+(2*8)+(1*4)=152
152 % 10 = 2
So 1309362-84-2 is a valid CAS Registry Number.

1309362-84-2Upstream product

1309362-84-2Downstream Products

1309362-84-2Relevant academic research and scientific papers

Tricalysionoside a, a megastigmane gentiobioside, sulfatricalysines a-F, and tricalysiosides X-Z, ent-kaurane glucosides, from the leaves of Tricalysia dubia

Shitamoto, Junko,Sugimoto, Sachiko,Matsunami, Katsuyoshi,Otsuka, Hideaki,Shinzato, Takakazu,Takeda, Yoshio

, p. 72 - 77 (2011)

Further isolation work on the water-soluble fraction of a MeOH extract of Tricalysia dubia afforded one new megastigmane gentiobioside, named tricalysionoside A (1), and three sulfates, named sulfatricalysines A-C (2-4). Extensive isolation work on the 1-BuOH-soluble fraction of a MeOH extract of T. dubia yielded sulfatricalysines D-F (5-7) and three new ent-kaurane glucosides, named tricalysiosides X-Z (8-10). The structures of the new compounds were elucidated by analyses of one- and two-dimensional NMR spectroscopic data. The absolute stereochemistry of tricalysionoside A (1) was established by modified Mosher's method.

Reinvestigation of the absolute stereochemistry of megastigmane glucoside, icariside B5

Matsunami, Katsuyoshi,Otsuka, Hideaki,Takeda, Yoshio,Miyase, Toshio

experimental part, p. 1399 - 1402 (2010/12/19)

Icariside B5 is one of the widely distributed megastigmane glucosides among plant sources. The absolute structure of icariside B 5 was reinvestigated by chemical conversion from the related compound and the application of the modifie

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