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((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid is a complex organic compound with a molecular formula of C23H26O6. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry at the 2nd, 3rd, 4th, and 5th carbon atoms, which are all in the S (2S), S (3S), R (4R), and R (5R) configurations, respectively. The compound features a tetrahydro-pyran ring, which is a type of cyclic ether, and is substituted with three benzyloxy groups at the 3rd, 4th, and 5th carbon atoms. The benzyloxy groups are derived from benzyl alcohol and are used to protect the hydroxyl groups in the molecule. The compound also has an acetic acid group attached to the 2-yl position of the tetrahydro-pyran ring, which contributes to its acidic properties. ((2S,3S,4R,5R)-3,4,5-Tris-benzyloxy-tetrahydro-pyran-2-yl)-acetic acid is often used in organic synthesis, particularly in the preparation of complex carbohydrates and other biologically active molecules, due to its ability to serve as a protected building block for these structures.

84781-71-5

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84781-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84781-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,8 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84781-71:
(7*8)+(6*4)+(5*7)+(4*8)+(3*1)+(2*7)+(1*1)=165
165 % 10 = 5
So 84781-71-5 is a valid CAS Registry Number.

84781-71-5Relevant academic research and scientific papers

Enantioselective Synthesis of Pseudomonic Acids. I. Synthesis of Key Intermediates

Schoenenberger, Bernhard,Summermatter, Walter,Ganter, Camille

, p. 2333 - 2337 (2007/10/02)

An enantioselective synthesis of key intermediates for the synthesis of the antimicrobially active pseudomonic acids A (1), B (2) and C (3) is described.D-Ribose (4) was used as starting material.

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