ChemicalBook--->CAS DataBase List--->194157-10-3

194157-10-3

194157-10-3 Structure

194157-10-3 Structure
IdentificationBack Directory
[Name]

4-Benzyloxy-3-methyl-phenol
[CAS]

194157-10-3
[Synonyms]

4-Benzyloxy-3-methyl-phenol
7-oxa-2-azaspiro[3.5]nona...
7-oxa-2-azaspiro[3.5]nonane (HCl)
7-Oxa-2-azaspiro[3.5]nonane (9CI)
7-Oxa-2-azaspiro[3.5]nonane HCl salt
7-oxa-2-azaspiro[3.5]nonane - X12040
7-Oxa-2-aza-spiro[3.5]nonane oxalate forM
7-oxa-2-azaspiro[3.5]nonane oxalic acid salt
[Molecular Formula]

C7H13NO
[MDL Number]

MFCD11204146
[MOL File]

194157-10-3.mol
[Molecular Weight]

127.18
Chemical PropertiesBack Directory
[Boiling point ]

208.4±40.0 °C(Predicted)
[density ]

1.04±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

10.49±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

7-Oxa-2-azaspiro[3.5]nonane is used in preparation of the zeste enhancer homolog 2 inhibitor and their medical applications.
[Synthesis]

The synthesis of 7-oxa-2-azaspiro[3.5]nonane is as follows: (1) under the condition of an acid binding agent, carrying out a first cyclization reaction on the compound 1 and the compound 2 in N, N-dimethylformamide under the action of a phase transfer catalyst and iodo metal salt to obtain a compound 3;(2) Carrying out a second cyclization reaction on the compound 3, lithium aluminum hydride and a reaction solvent to obtain the product.
7-oxa-2-azaspiro[3.5]nonane synthesis route
Spectrum DetailBack Directory
[Spectrum Detail]

4-Benzyloxy-3-methyl-phenol(194157-10-3)1HNMR
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