What is the endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol?

endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol is , while it's Molecular Formula is C10H19 N O. (1R,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-ol is an intermediate for the synthesis of (S)-(1R,3r,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-yl 3-Hydroxy-2-phenylpropanoate (I824270), which is a compound that can be synthesized from Atropine (A794630), a nerve agent that occurs naturally in plants of the nightshade family.

What is the CAS number for endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol?

The CAS number of endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol is 3423-25-4.

What is endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol (3423-25-4) used for?

endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol, also known as (1R,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-ol, is an organic compound with a unique bicyclic structure and an alcohol functional group. It is characterized by its stereochemistry, with the 1R,5S configuration, and the presence of an isopropyl group at the 8-position. endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol serves as a crucial intermediate in the synthesis of various pharmaceutically relevant molecules.InChI:InChI=1/C10H19NO/c1-7(2)11-8-3-4-9(11)6-10(12)5-8/h7-10,12H,3-6H2,1-2H3

What is the endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol?

endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol is , while it's Molecular Formula is C10H19 N O. (1R,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-ol is an intermediate for the synthesis of (S)-(1R,3r,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-yl 3-Hydroxy-2-phenylpropanoate (I824270), which is a compound that can be synthesized from Atropine (A794630), a nerve agent that occurs naturally in plants of the nightshade family.

What is the CAS number for endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol?

The CAS number of endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol is 3423-25-4.

What is endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol (3423-25-4) used for?

endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol, also known as (1R,5S)-8-Isopropyl-8-azabicyclo[3.2.1]octan-3-ol, is an organic compound with a unique bicyclic structure and an alcohol functional group. It is characterized by its stereochemistry, with the 1R,5S configuration, and the presence of an isopropyl group at the 8-position. endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol serves as a crucial intermediate in the synthesis of various pharmaceutically relevant molecules.InChI:InChI=1/C10H19NO/c1-7(2)11-8-3-4-9(11)6-10(12)5-8/h7-10,12H,3-6H2,1-2H3

3423-25-4

8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol

Another Name：

CasNo.： 3423-25-4

MF： C10H19 N O

MW： 169.267

Storage：

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ch_Name： 8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol

English name： 8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol

CasNo.： 3423-25-4

MF： C10H19 N O

MW： 169.267

Quality Manufacturer Supply High Purity 99% 8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol 3423-25-4 with Reasonable Price

Molecular Formula:C10H19 N O
Molecular Weight:169.267
Vapor Pressure:0.00115mmHg at 25°C
Boiling Point:266.9±15.0℃ (760 Torr)
PKA:14.84±0.20(Predicted)
Flash Point:89.7±14.5℃
PSA：23.47000
Density:1.037±0.06 g/cm3 (20 ºC 760 Torr)
LogP:1.32040

endo-8-isopropyl-8-azabicyclo[3.2.1]octan-3-ol(Cas 3423-25-4) Usage

InChI:InChI=1/C10H19NO/c1-7(2)11-8-3-4-9(11)6-10(12)5-8/h7-10,12H,3-6H2,1-2H3

3423-25-4 Relevant articles

Metabolism of N-alkyldiamines and N-alkylnortropinones by transformed root cultures of Nicotiana and Brugmansia

Boswell, Henry D.,Draeger, Birgit,Eagles, John,McClintock, Carol,Parr, Adrian,Portsteffen, Andreas,Robins, David J.,Robins, Richard J.,Walton, Nicholas J.,Wong, Chi

, p. 855 - 869 (2007/10/03)

A range of analogues of N-methylputresci...

Specificities of the enzymes of N-alkyltropane biosynthesis in Brugmansia and Datura

Boswell, Henry D.,Draì?ger, Birgit,McLauchlan, W. Russell,Portsteffen, Andreas,Robins, David J.,Robins, Richard J.,Walton, Nicholas J.

, p. 871 - 878 (2007/10/03)

The enzymes N-methylputrescine oxidase (...

Conveniant Method for Replacement of Tertiary N-Methyl by Other Alkyl Groups: Application to Morphine Alkaloids

Manoharan, T. Samuel,Madyastha, K. Madhava,Singh, B. B.,Bhatnagar, S. P.,Weiss, Ulrich

, p. 5 - 11 (2007/10/02)

The replacement of N-methyl of N-methylp...

PHOSPHINERHODIUM COMPLEXES AS HOMOGENEOUS CATALYSTS. XVI. STEREOSELECTIVE HYDROGENATION OF CYCLIC KETONES

Toros, Szilard,Kollar, Laszlo,Heil, Balint,Marko, Laszlo

, p. 377 - 384 (2007/10/02)

Cyclic ketones have been hydrogenated st...

3423-25-4 Process route

: 93713-44-1
(1R,3R,5S)-3-Hydroxy-8-isopropyl-8-methyl-8-azonia-bicyclo[3.2.1]octane; iodide

: 3423-25-4
endo-8-(1-methylethyl)-8-azabicyclo<3.2.1>octan-3-ol

: 120-29-6
3-tropanol

Conditions

Conditions	Yield
With sodium thiophenolate; In acetonitrile; butanone; Heating;	40% 13%

: 3-oxo-8-propyl-8-aza-bicyclo[3.2.1]octane-2,4-dicarboxylic acid

: 3423-25-4
endo-8-(1-methylethyl)-8-azabicyclo<3.2.1>octan-3-ol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 6 M HCl / 1 h / 70 °C 2: Brugmansia candida x aurea / Enzymatic reaction With hydrogenchloride; Brugmansia candida x aurea; 1: Decarboxylation / 2: Reduction;

3423-25-4 Upstream products

3423-28-7
8-aza-8-isopropyl-bicyclo<3.2.1>octan-3-one
93713-44-1
(1R,3R,5S)-3-Hydroxy-8-isopropyl-8-methyl-8-azonia-bicyclo[3.2.1]octane; iodide

3423-25-4 Downstream products

58005-18-8
3-hydroxy-8-isopropyl-8-methyl-8-azonia-bicyclo[3.2.1]octane; bromide
145450-34-6
(1R,2S)-2-Phenyl-cyclohexanecarboxylic acid (1R,3R,5S)-8-isopropyl-8-aza-bicyclo[3.2.1]oct-3-yl ester
145450-03-9
(1R,3R,5S,8R)-8-Isopropyl-3-(2-phenyl-cyclohex-2-enecarbonyloxy)-8-propyl-8-azonia-bicyclo[3.2.1]octane; iodide
145449-89-4
(1R,3R,5S,8R)-8-Ethyl-8-isopropyl-3-(2-phenyl-cyclohex-2-enecarbonyloxy)-8-azonia-bicyclo[3.2.1]octane; iodide