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(2S,4R)-4-Benzyloxy-hept-6-ene-1,2-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

205372-01-6

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205372-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205372-01-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,3,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 205372-01:
(8*2)+(7*0)+(6*5)+(5*3)+(4*7)+(3*2)+(2*0)+(1*1)=96
96 % 10 = 6
So 205372-01-6 is a valid CAS Registry Number.

205372-01-6Relevant articles and documents

Studies directed towards the total synthesis of feigrisolide B

Sharma,Kumar, K. Raman

, p. 2323 - 2326 (2007/10/03)

Attempts directed towards the total synthesis of feigrisolide B resulted in the synthesis of lactones 1 and 2. The synthesis of 1 and 2 was achieved from d-glucose and l-malic acid, respectively, with a Ti(IV) mediated diastereoselective aldol reaction as

Studies on the stereochemistry of theonezolides A-C1: Elucidation of the relative configurations of 1,3-diol moieties of the C-4 ~ C-17 fragment

Kobayashi, Jun'ichi,Yonezawa, Makiko,Takeuchi, Shinji,Ishibashi, Masami

, p. 39 - 42 (2007/10/03)

Four model compounds having syn and anti 1,3-diol type moieties corresponding to C-8/C-10 and C-14/C-16 positions contained in the C-4 ~ C-17 fragment of theonezolides A-C were prepared. Comparison of their spectral data suggested that the 1,3-diol at C-8/C-10 and the OH/OMe groups at C-14/C-16 positions of theonezolides A-C were both syn.

A synthesis of a C1-C7 building block for the enantiomer of hennoxazole A utilizing a regioselective ring opening of a cyclic acetal

Shioiri, Takayuki,McFarlane, Nigel,Hamada, Yasumasa

, p. 73 - 76 (2007/10/03)

AC1-C7 building block (4) for the enantiomer of hennoxazole A(1), an antivirus and analgesic active marine natural product, was efficiently synthesized from (S)-malic acid utilizing the following key steps: (1) the stereoselective co

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