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2-Boc-5-hydroxy-2-azaspiro[3.3]heptane is a unique chemical compound featuring a cycloalkane ring with a nitrogen atom and a spirobicyclic moiety. Characterized by the presence of a hydroxy group and a tert-butoxycarbonyl (Boc) protecting group, 2-Boc-5-hydroxy-2-azaspiro[3.3]heptane is known for its structural rigidity and reactivity, making it a valuable building block in organic synthesis and drug discovery.

1330764-31-2

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1330764-31-2 Usage

Uses

Used in Organic Synthesis:
2-Boc-5-hydroxy-2-azaspiro[3.3]heptane is used as a building block for the synthesis of complex organic molecules. Its unique structure and reactivity, along with the Boc protecting group, allow for selective manipulation of the hydroxy group during reactions, facilitating the creation of diverse molecular architectures.
Used in Drug Discovery:
In the pharmaceutical industry, 2-Boc-5-hydroxy-2-azaspiro[3.3]heptane is utilized as a key intermediate in the development of new drugs. The spirobicyclic structure contributes to its enhanced biological activity and drug-like properties, making it a promising candidate for the design of novel therapeutic agents.
Used in Chemical Research:
2-Boc-5-hydroxy-2-azaspiro[3.3]heptane serves as an important compound in the field of chemical research, providing insights into the synthesis and properties of complex molecules. Its unique features make it a valuable tool for studying reaction mechanisms and exploring new synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1330764-31-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,7,6 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1330764-31:
(9*1)+(8*3)+(7*3)+(6*0)+(5*7)+(4*6)+(3*4)+(2*3)+(1*1)=132
132 % 10 = 2
So 1330764-31-2 is a valid CAS Registry Number.

1330764-31-2Downstream Products

1330764-31-2Relevant academic research and scientific papers

Practical Synthesis of Fluorinated Piperidine Analogues Based on the 2-Azaspiro[33]heptane Scaffold

Chernykh, Anton V.,Tkachenko, Anton N.,Feskov, Illia O.,Daniliuc, Constantin G.,Tolmachova, Nataliya A.,Volochnyuk, Dmitriy M.,Radchenko, Dmytro S.

, p. 1824 - 1827 (2016)

The synthesis of a set of conformationally restricted fluorinated analogues of piperidine, based on a 2-azaspiro[3.3]heptane scaffold, is reported. Different pattern of fluorine substitution within the rigid skeleton make the analogues excellent candidate

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