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(1S,4S,5R,8R)-4-azido-8-benzyloxy-3-methoxy-2,6-dioxabicyclo[3.3.0]octane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849624-15-3

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849624-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849624-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,6,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 849624-15:
(8*8)+(7*4)+(6*9)+(5*6)+(4*2)+(3*4)+(2*1)+(1*5)=203
203 % 10 = 3
So 849624-15-3 is a valid CAS Registry Number.

849624-15-3Relevant academic research and scientific papers

Formal synthesis of furanodictine B from D-glucose

Mereyala, Hari Babu,Baseeruddin, Mohd,Reddy Koduru, Sreenivasulu

, p. 3457 - 3460 (2004)

Formal synthesis of furanodictine B is described starting from d-glucose. An efficient formal synthesis of furanodictine B 1b is described starting from d-glucose. The synthetic protocol is based on deriving the bicyclic intermediate 2 from d-glucose by a

Stereodivergent synthesis of new amino sugars, furanodictines A and B, starting from d-glucuronolactone

Matsuura, Daisuke,Mitsui, Takeshi,Sengoku, Tetsuya,Takahashi, Masaki,Yoda, Hidemi

experimental part, p. 11686 - 11696 (2009/04/06)

An efficient and divergent strategy for the total synthesis of the first 3,6-dihydroaminosugars, furanodictines A (2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-d-glucofuranose) and B (2-acetamido-3,6-anhydro-2-deoxy-5-O-isovaleryl-d-mannofuranose), has been developed. The synthetic process is featured by readily accessible and stereodefined manipulation of highly functionalized bicyclic tetrahydrofuran derivatives incorporating the glucuronolactone (common starting material)-derived skeleton.

An efficient and straightforward synthetic process to an amino sugar analogue, furanodictine B

Matsuura, Daisuke,Nojiri, Tomoko,Suzuki, Yuji,Takabe, Kunihiko,Yoda, Hidemi

, p. 287 - 288 (2007/10/03)

A convenient and practical strategy for the construction of a natural amino sugar analogue, furanodictine B, isolated from the multicellular fruit body has been developed in an optically active form. The synthetic process is based on readily accessible and stereodefmed manipulation of the highly functionalized bicyclic derivative incorporating the glucuronolactone-derived skeleton.

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