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2-Boc-6-oxo-2-azaspiro[3.4]octane is a spirocyclic chemical compound with the molecular formula C13H21NO3. It features a bicyclic structure with a bridgehead carbon atom and a tert-butyloxycarbonyl (Boc) protecting group, which is used to protect amines in organic synthesis. The presence of an "oxo" group signifies the inclusion of a ketone functional group. 2-Boc-6-oxo-2-azaspiro[3.4]octane is valued for its unique spirocyclic structure and its potential as a pharmacophore in the design of pharmaceuticals and biologically active molecules.

1363382-39-1

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1363382-39-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Boc-6-oxo-2-azaspiro[3.4]octane is used as a building block in the synthesis of various pharmaceuticals for its unique spirocyclic structure, which can contribute to the development of new drugs with enhanced properties.
Used in Drug Design:
In drug design, 2-Boc-6-oxo-2-azaspiro[3.4]octane is utilized as a pharmacophore, a key element in the design of biologically active molecules, due to its potential to interact with biological targets and influence drug efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1363382-39-1 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 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1363382-39:
(9*1)+(8*3)+(7*6)+(6*3)+(5*3)+(4*8)+(3*2)+(2*3)+(1*9)=161
161 % 10 = 1
So 1363382-39-1 is a valid CAS Registry Number.

1363382-39-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 6-oxo-2-azaspiro[3.4]octane-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1363382-39-1 SDS

1363382-39-1Downstream Products

1363382-39-1Relevant articles and documents

Facile synthesis of 2-azaspiro[3.4]octane

Ramesh, Subbiah,Balakumar, Ramadas,Rizzo, John R.,Zhang, Tony Y.

, p. 3056 - 3065 (2019/03/21)

Our annulation strategy utilized for the synthesis of 2-azaspiro[3.4]octane is explained. Three successful routes for the synthesis were developed. One of the approaches involved annulation of the cyclopentane ring and the remaining two approaches involved annulation of the four membered ring. All three approaches employ readily available starting materials with conventional chemical transformations and minimal chromatographic purifications to afford the title compound. The merits and limitations of the three approaches are also discussed.

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