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The chemical compound "(1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol methanesulfonate" is a complex organic molecule with a unique stereochemistry and functional groups. It features a cyclopentenol core, which is a five-membered ring with a hydroxyl group at the 1-position. The molecule is chiral, with the specific configuration of the chiral centers being (1S,4R,5S), indicating the arrangement of atoms around these centers. A benzyloxymethyl group is attached at the 3-position, providing a protecting group and a potential site for further chemical reactions. The 4,5-O-isopropylidene group serves as a protecting group for the hydroxyl groups at the 4 and 5 positions, preventing unwanted side reactions. Finally, the methanesulfonate group is a good leaving group, often used in organic synthesis to facilitate substitution reactions. (1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol methanesulfonate is likely used in advanced organic synthesis, particularly in the preparation of complex natural products or pharmaceuticals, due to its intricate structure and the potential for selective reactions at specific sites.

89291-77-0

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89291-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89291-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,9 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89291-77:
(7*8)+(6*9)+(5*2)+(4*9)+(3*1)+(2*7)+(1*7)=180
180 % 10 = 0
So 89291-77-0 is a valid CAS Registry Number.

89291-77-0Downstream Products

89291-77-0Relevant academic research and scientific papers

Total Synthesis of (-)-Neplanocin A

Marquez, Victor E.,Lim, Mu-Ill,Tseng, Christopher K.-H.,Markovac, Anica,Priest, Matthew A.,et al.

, p. 5709 - 5714 (2007/10/02)

An efficient synthesis of neplanocin A, which is easily adaptable for the preparation of other cyclopentenyl containing nucleoside isosteres, has been developed.This enantioselective synthesis provides control of two of the three chiral centers of neplano

SYNTHESIS OF THE CARBOCYCLIC NUCLEOSIDE (-)-NEPLANOCIN A

Medich, John R.,Kunnen, Kevin B.,Johnson, Carl R.

, p. 4131 - 4134 (2007/10/02)

(-)-Neplanocin A has been prepared in 14 steps from cyclopentadiene (11percent overall yield).

TOTAL SYNTHESIS OF (-)-NEPLANOCIN A

Lim, Mu-ill,Marquez, Victor E.

, p. 5559 - 5562 (2007/10/02)

A total synthesis of (-)-neplanocin A has been accomplished in 15 steps starting from the readily available D-(+)-ribonic acid γ-lactone.

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