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2-phenylazepane (HCl), also known as 2-phenyl-1-azabicyclo[2.2.2]octane hydrochloride, is a chemical compound with the molecular formula C14H20ClN. It is a white crystalline solid that is soluble in water and various organic solvents. 2-phenylazepane (HCl) is primarily used as a pharmaceutical intermediate, specifically in the synthesis of certain drugs, such as anxiolytics and antidepressants. The hydrochloride salt form of 2-phenylazepane enhances its solubility and stability, making it more suitable for pharmaceutical applications. It is important to note that handling and storage of 2-phenylazepane (HCl) should be done with proper safety measures, as it may have potential health risks and environmental impacts.

3466-83-9

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3466-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3466-83-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3466-83:
(6*3)+(5*4)+(4*6)+(3*6)+(2*8)+(1*3)=99
99 % 10 = 9
So 3466-83-9 is a valid CAS Registry Number.

3466-83-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-hexahydro-azepine, hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Phenyl-hexahydro-azepin, Hydrochlorid

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:3466-83-9 SDS

3466-83-9Relevant academic research and scientific papers

Chemoenzymatic Synthesis of Substituted Azepanes by Sequential Biocatalytic Reduction and Organolithium-Mediated Rearrangement

Zawodny, Wojciech,Montgomery, Sarah L.,Marshall, James R.,Finnigan, James D.,Turner, Nicholas J.,Clayden, Jonathan

, p. 17872 - 17877 (2018)

Enantioenriched 2-aryl azepanes and 2-arylbenzazepines were generated biocatalytically by asymmetric reductive amination using imine reductases or by deracemization using monoamine oxidases. The amines were converted to the corresponding N′-aryl ureas, which rearranged on treatment with base with stereospecific transfer of the aryl substituent to the 2-position of the heterocycle via a configurationally stable benzyllithium intermediate. The products are previously inaccessible enantioenriched 2,2-disubstituted azepanes and benzazepines.

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