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8-Azabicyclo(3.2.1)octan-3-ol, 8-methylacetate (ester), exo- is a complex organic compound with the molecular formula C10H19NO2. It is a derivative of 8-azabicyclo[3.2.1]octane, a bicyclic amine, where one of the hydrogen atoms on the nitrogen is replaced by a methyl group, and the hydroxyl group is esterified with acetic acid. The "exo" prefix indicates that the acetate group is attached to the exocyclic carbon, which is the carbon not part of the ring structure. 8-Azabicyclo(3.2.1)octan-3-ol, 8-methylacetate (ester), exo- is known for its unique structure and potential applications in pharmaceuticals and chemical research, particularly in the synthesis of complex molecules and as a building block for more intricate organic compounds.

3423-26-5

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3423-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3423-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3423-26:
(6*3)+(5*4)+(4*2)+(3*3)+(2*2)+(1*6)=65
65 % 10 = 5
So 3423-26-5 is a valid CAS Registry Number.

3423-26-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) acetate

1.2 Other means of identification

Product number -
Other names Acetylpseudotropine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3423-26-5 SDS

3423-26-5Downstream Products

3423-26-5Relevant academic research and scientific papers

METHODS FOR ONE-POT N-DEMETHYLATION/N-ACYLATION OF MORPHINE AND TROPANE ALKALOIDS

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Page/Page column 4; 7, (2009/01/24)

The present invention provides a method for the N-demethylation and/or N-acylation of an N-methylated heterocycle such as morphine alkaloids or tropane alkaloids. The method comprises reacting the heterocycle with an acylating agent in the presence of a m

TOCOLYTIC OXYTOCIN RECEPTOR ANTAGONISTS

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, (2008/06/13)

This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery. A typical compound is as follows: STR1

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