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1363382-39-1

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1363382-39-1 Usage

General Description

2-Boc-6-oxo-2-azaspiro[3.4]octane is a chemical compound with the molecular formula C13H21NO3. It is a spirocyclic compound, meaning it contains a bicyclic structure with a bridgehead carbon atom. The "Boc" in its name refers to the tert-butyloxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines. The presence of the "oxo" group indicates the presence of a ketone functional group. 2-Boc-6-oxo-2-azaspiro[3.4]octane is often utilized as a building block in the synthesis of various pharmaceuticals and biologically active molecules due to its unique spirocyclic structure and its potential to act as a pharmacophore in drug design.

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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