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(1R,3S,4R,5R,8S)-4-Amino-3-benzyloxy-2,6-dioxa-bicyclo[3.2.1]octan-8-ol is a complex chemical compound with a bicyclic structure. It contains an amino group, a benzyloxy group, and a hydroxyl group, making it a versatile molecule with potential applications in pharmaceuticals and organic synthesis. The stereochemistry of the compound is specified by the "1R,3S,4R,5R,8S" notation, indicating the spatial arrangement of the substituent groups around the bicyclic ring. As a result of its unique structure, (1R,3S,4R,5R,8S)-4-Amino-3-benzyloxy-2,6-dioxa-bicyclo[3.2.1]octan-8-ol may exhibit specific biological activities and could serve as a building block for the synthesis of more complex molecules.

117701-88-9

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117701-88-9 Usage

Uses

Used in Pharmaceutical Industry:
(1R,3S,4R,5R,8S)-4-Amino-3-benzyloxy-2,6-dioxa-bicyclo[3.2.1]octan-8-ol is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and functional groups allow for the design and synthesis of various drug candidates with potential therapeutic applications.
Used in Organic Synthesis:
(1R,3S,4R,5R,8S)-4-Amino-3-benzyloxy-2,6-dioxa-bicyclo[3.2.1]octan-8-ol is used as a building block in organic synthesis for the creation of more complex molecules. Its versatile structure and functional groups enable the formation of a wide range of chemical compounds with diverse properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 117701-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,7,0 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117701-88:
(8*1)+(7*1)+(6*7)+(5*7)+(4*0)+(3*1)+(2*8)+(1*8)=119
119 % 10 = 9
So 117701-88-9 is a valid CAS Registry Number.

117701-88-9Relevant academic research and scientific papers

UEBER EINE UNGEWOEHNLICHE REAKTION DER 2-DESOXY-2-TRIMETHYLAMMONIO-D-GLUCOSE

Reckendorf, Wolfgang Meyer zu,Sandner, Stefan

, p. 2047 - 2050 (2007/10/02)

The alkaline hydrolysis of 2-deoxy-1,3,4,6-tetra-O-acetyl-2-trimethylammonio-α-D-glucopyranose chloride leads to an unexpected product.Contrary to the hydrolysis under acidic conditions yielding 2-deoxy-2-trimethylammonio-D-glucose we obtained the corresponding 3,6-anhydro derivative by reaction with sodium hydroxide or ammonia in methanol.

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