Tert-butyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate

Catalog Number	ACM185099676-1
CAS Number	185099-67-6
Structure
Synonyms	N-(tert-Butoxycarbonyl)nortropinone
Molecular Weight	225.28
InChI	InChI=1S/C12H19NO3/c1-12(2,3)16-11(15)13-8-4-5-9(13)7-10(14)6-8/h8-9H,4-7H2,1-3H3
InChI Key	MENILFUADYEXNU-UHFFFAOYSA-N
Melting Point	70-74 °C
Purity	98%+
Complexity	303
Covalently-Bonded Unit Count	1
Defined Atom Stereocenter Count	0
Exact Mass	225.13649347
Heavy Atom Count	16
Hydrogen Bond Acceptor Count	3
Hydrogen Bond Donor Count	0
Monoisotopic Mass	225.13649347
PhysicalState	Solid
Rotatable Bond Count	2
Topological Polar Surface Area	46.6 Ų

Custom Q&A

What is the chemical formula of N-Boc-Nortropinone?

The chemical formula of N-Boc-Nortropinone is C12H19NO3.

What is the molecular weight of N-Boc-Nortropinone?

The molecular weight of N-Boc-Nortropinone is 225.28.

What is the melting point of N-Boc-Nortropinone?

The melting point of N-Boc-Nortropinone is 70-74 °C.

How should N-Boc-Nortropinone be stored?

N-Boc-Nortropinone should be kept in a dark place, sealed in dry conditions, at room temperature.

What is the solubility of N-Boc-Nortropinone in chloroform and methanol?

N-Boc-Nortropinone is slightly soluble in chloroform and methanol.

What is the hazard class of N-Boc-Nortropinone?

The hazard class of N-Boc-Nortropinone is irritant.

What is the usage of N-Boc-Nortropinone?

N-Boc-Nortropinone is a 8-azabicyclo[3.2.1]octane derivative useful as an opioid receptor modulator.

What can N-Boc-Nortropinone be used for in terms of chemical synthesis?

N-Boc-Nortropinone can be used for the preparation of Tropine derivatives.

Why are Tropine derivatives important in various industries?

Tropine and its derivatives are important alkaloids present in natural plants with diverse biological activities, widely used in the fields of pesticides, pharmaceuticals, and chemical industries.

How can N-Boc-Nortropinone be used to synthesize a new bicyclic vinyl boronate?

N-Boc-Nortropinone can be used to synthesize a new bicyclic vinyl boronate through a specific methodology involving aryl-substituted nortropanes.

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