(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol
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![(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/902324ee16c94c2581b6483cb2a7a897.png "(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol")
(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol
structure -
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CAS No:
3423-25-4
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Formula:
C10H19NO
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Chemical Name:
(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol
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Synonyms:
8-Azabicyclo[3.2.1]octan-3-ol,8-(1-methylethyl)-,(3-endo)-;1αH,5αH-Nortropan-3α-ol,8-isopropyl-;8-Azabicyclo[3.2.1]octan-3-ol,8-(1-methylethyl)-,endo-;Nortropine,8-isopropyl-;(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol;8-Isopropylnortropan-3α-ol;N-Isopropylnortropine
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CAS No:
(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol Basic Attributes
169.26396
169.26
222-314-9
2933990090
Safety Information
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory.
(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol Use and Manufacturing
Add succinaldehyde, isopropylamine hydrochloride, and acetone dicarboxylic acid with the participation of sodium acetate, condensation and decarboxylation to generate isopropyl nortropine, which is then hydrogenated under active nickel catalysis.
Isopropyl atropine intermediate.
Computed Properties
Molecular Weight:169.26
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:169.146664230
Monoisotopic Mass:169.146664230
Topological Polar Surface Area:23.5
Heavy Atom Count:12
Complexity:155
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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(3-endo)-8-(1-Methylethyl)-8-azabicyclo[3.2.1]octan-3-ol
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