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2-Boc-2-aza-spiro[3.3]heptane-6-Methanol, also known as Boc-protected 2-azabicyclo[2.2.1]heptane-6-methanol, is a complex organic compound with the chemical formula C14H25NO3. It features a spirocyclic compound structure with a 2-azabicyclo[2.2.1]heptane core and a Boc (tert-butoxycarbonyl) protecting group. 2-Boc-2-aza-spiro[3.3]heptane-6-Methanol is recognized for its unique chemical and physical properties, which make it a valuable intermediate in the field of organic synthesis.

1363381-93-4

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1363381-93-4 Usage

Uses

Used in Pharmaceutical Industry:
2-Boc-2-aza-spiro[3.3]heptane-6-Methanol is used as a building block in organic synthesis for the production of various drugs. The Boc protecting group allows for selective reactions and manipulation of the compound's structure, which is crucial in drug discovery and development. This feature makes it a versatile intermediate for creating diverse molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the realm of organic synthesis, 2-Boc-2-aza-spiro[3.3]heptane-6-Methanol is utilized as a key intermediate. Its spirocyclic nature provides unique structural features that can be exploited to synthesize a wide range of complex organic molecules, contributing to the advancement of chemical research and the creation of new compounds with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1363381-93-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,3,8 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1363381-93:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*8)+(3*1)+(2*9)+(1*3)=164
164 % 10 = 4
So 1363381-93-4 is a valid CAS Registry Number.

1363381-93-4Downstream Products

1363381-93-4Relevant academic research and scientific papers

Regioselective Monoborylation of Spirocyclobutenes

Nóvoa, Luis,Trulli, Laura,Fernández, Israel,Parra, Alejandro,Tortosa, Mariola

, p. 7434 - 7438 (2021/10/02)

We present a strategy for the synthesis of spirocyclic cyclobutanes with modulable exit vectors based on the regioselective monoborylation of spirocyclobutenes. Using an inexpensive copper salt and a commercially available bidentate phosphine, a broad variety of borylated spirocycles have been prepared with complete regiocontrol. The boryl moiety provides a synthetic handled for further functionalization, allowing access to a wide array of spirocyclic building blocks from a common intermediate.

ANTAGONISTS OF THE MUSCARINIC ACETYLCHOLINE RECEPTOR M4

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Paragraph 00221, (2019/07/13)

Disclosed herein are substituted 2-azaspiro[3.3]heptane compounds, which may be useful as antagonists of the muscarinic acetylcholine receptor M4 (mAChR M4). Also disclosed herein are methods of making the compounds, pharmaceutical c

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