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51179-05-6

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51179-05-6 Usage

General Description

2-(4-Benzyloxy-phenyl)-ethylamine is a chemical compound with the formula C16H19NO. It is an organic compound that belongs to the class of ethylamines. This chemical is commonly used in pharmaceutical and research applications due to its potential biological activities. It is known to have interactions with serotonin receptors and may have potential applications in the treatment of various medical conditions. As a result, it is a compound of interest in the field of pharmacology and drug discovery. Additionally, it is important to handle this compound with care, as it may pose health and safety hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 51179-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,7 and 9 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51179-05:
(7*5)+(6*1)+(5*1)+(4*7)+(3*9)+(2*0)+(1*5)=106
106 % 10 = 6
So 51179-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO/c16-11-10-13-6-8-15(9-7-13)17-12-14-4-2-1-3-5-14/h1-9H,10-12,16H2

51179-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-phenylmethoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names 2-(2-CHLORO-ACETYLAMINO)-4-(5-METHYL-FURAN-2-YL)-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER

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:51179-05-6 SDS

51179-05-6Relevant articles and documents

Enantioselective Sequential-Flow Synthesis of Baclofen Precursor via Asymmetric 1,4-Addition and Chemoselective Hydrogenation on Platinum/Carbon/Calcium Phosphate Composites

Furiya, Yuichi,Ishitani, Haruro,Kobayashi, Shu

supporting information, (2020/05/05)

Continuous-flow synthesis of baclofen precursor (2) was achieved using achiral and chiral heterogeneous catalysts in high yield with high enantioselectivity. The key steps are chiral calcium-catalyzed asymmetric 1,4-addition of a malonate to a nitroalkene and chemoselective reduction of a nitro compound to the corresponding amino compound by using molecular hydrogen. A dimethylpolysilane (DMPS)-modified platinum catalyst supported on activated carbon (AC) and calcium phosphate (CP) has been developed that has remarkable activity for the selective hydrogenation of nitro compounds.

SYNTHESIS OF POLYCYCLIC ALKALOIDS

-

, (2013/09/26)

Disclosed embodiments concern polycyclic alkaloid compounds and methods for their use and synthesis. Particular embodiments concern polycyclic alkaloids having a fused, six-membered ring, while other embodiments concern polycyclic alkaloids having a fused

PTERIDINES AND THEIR USE AS AGROCHEMICALS

-

, (2011/04/14)

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.

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