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2-Azaspiro[4.5]decane hemioxlate, 95%|1175510|176-66-9

2-Azaspiro[4.5]decane hemioxlate, 95%

Cat. No JK1175510_100_MG
J&K Chemical

Product Information

Product Name
2-Azaspiro4.5decane hemioxlate, 95%
Brand Name
J&K
Product Number
1175510
CAS
176-66-9
Molecular Formula
C9H17N·0.5C2H2O4
Molecular Weight
184.25
SDS Document
View/Download
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
418822
IUPAC Name
2-azaspiro4.5decane
InChI Key
SFCOKGCNIPSUQF-UHFFFAOYSA-N
SMILES
C1CCC2(CC1)CCNC2

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

Photocatalyzed Formation of Heterocycles
Publication Name: Free-Radical Synthesis and Functionalization of Heterocycles
Publication Date: 2018
DOI: 10.1007/7081_2017_13

A simple and efficient route for the synthesis of novel isoxazolyl-2-azaspiro[4.5][4.5][4.5]deca-1,6,9-trien-8-ones by condensation of 2,6-dimethylphenol with isobutyraldehyde and nitriles
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2012-01
DOI: 10.1134/s1070428012010101

Spirocyclohexadienones: X. Three-component condesation of 1,2,3- and 1,2,4-trimethoxybenzenes with cyclohexanecarbaldehyde and nitriles. Synthesis of 1,2- and 1,4-dimethoxy-14-azadispiro[5.1.5.2]pentadeca-1,4-dien-3-ones
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2009-03
DOI: 10.1134/s1070428009030038

Synthesis, Physicochemical and Anticonvulsant Properties of New N‐(Pyridine‐2‐yl) Derivatives of 2‐Azaspiro[4.4]nonane and [4.5]decane‐1,3‐dione. Part II
Publication Name: Archiv der Pharmazie
Publication Date: 2006-04-28
DOI: 10.1002/ardp.200500219

2-Azaspiro[4.5]decane hemioxlate, 95%

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