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185-69-3

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185-69-3 Usage

General Description

1-Azaspiro[2.5]octane, also known as homotropane, is a bicyclic heterocyclic organic compound. It possesses a seven-membered, nitrogen-containing ring and is used in the synthesis of pharmaceuticals and agrochemicals. This chemical has been studied for its potential use as a selective norepinephrine reuptake inhibitor and has shown promise in the treatment of conditions like depression, anxiety, and attention-deficit hyperactivity disorder. Additionally, 1-Azaspiro[2.5]octane has been investigated for its potential as a chiral ligand and as a building block for the synthesis of complex organic molecules. The compound has shown to have a wide range of applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 185-69-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185-69:
(5*1)+(4*8)+(3*5)+(2*6)+(1*9)=73
73 % 10 = 3
So 185-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-2-4-7(5-3-1)6-8-7/h8H,1-6H2

185-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Azaspiro[2.5]octane

1.2 Other means of identification

Product number -
Other names 2-azaspiro[2.5]octane

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:185-69-3 SDS

185-69-3Relevant articles and documents

Modular, One-Pot, Sequential Aziridine Ring Opening-SNAr Strategy to 7-, 10-, and 11-Membered Benzo-Fused Sultams

Loh, Joanna K.,Asad, Naeem,Samarakoon, Thiwanka B.,Hanson, Paul R.

, p. 9926 - 9941 (2015/11/03)

The generation of common and stereochemically rich medium-sized benzo-fused sultams via complementary pairing of heretofore-unknown (o-fluoroaryl)sulfonyl aziridine building blocks with an array of amino alcohols/amines in a modular one-pot, sequential protocol using an aziridine ring opening and intramolecular nucleophilic aromatic substitution is reported. The strategy employs a variety of amino alcohols/amines and proceeds with 6 + 4/6 + 5 and 6 + 1 cycloetherification pathways in a highly chemo- and regioselective fashion to obtain skeletally and structurally diverse, polycyclic, 10- to 11- and 7-membered benzo-fused sultams for broad-scale screening.

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