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16728-64-6

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16728-64-6 Usage

Synthesis Reference(s)

Synthesis, p. 590, 1975 DOI: 10.1055/s-1975-23843

Check Digit Verification of cas no

The CAS Registry Mumber 16728-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16728-64:
(7*1)+(6*6)+(5*7)+(4*2)+(3*8)+(2*6)+(1*4)=126
126 % 10 = 6
So 16728-64-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO/c11-7-4-8-12-9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9,11H2

16728-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Benzyloxy)propan-1-amine

1.2 Other means of identification

Product number -
Other names 3-phenylmethoxypropan-1-amine

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:16728-64-6 SDS

16728-64-6Relevant articles and documents

Highly efficient nitrobenzene and alkyl/aryl azide reduction in stainless steel jars without catalyst addition

Martina, Katia,Baricco, Francesca,Tagliapietra, Silvia,Moran, Maria Jesus,Cravotto, Giancarlo,Cintas, Pedro

supporting information, p. 18881 - 18888 (2018/11/26)

The mechanochemical and selective reduction of aryl nitro and aryl/alkyl azide derivatives, with either formate salts or hydrazine, to the corresponding, synthetically useful amines occurs in excellent yields in a planetary ball mill without the addition of a catalyst. This newly developed and solvent-free protocol is efficient, fast and does not require the addition of a metal hydrogenation catalyst as the stainless steel jar itself fulfils that role. The method has been applied to a broad range of compounds and excellent yields have been obtained. The formylation of alkyl amines has been successfully performed, by means of mechanochemical activation, in the presence of ammonium formate alone.

An Iodine-Catalyzed Hofmann-L?ffler Reaction

Martínez, Claudio,Mu?iz, Kilian

supporting information, p. 8287 - 8291 (2015/07/07)

Iodine reagents have been identified as economically and ecologically benign alternatives to transition metals, although their application as molecular catalysts in challenging C-H oxidation reactions has remained elusive. An attractive iodine oxidation catalysis is now shown to promote the convenient conversion of carbon-hydrogen bonds into carbon-nitrogen bonds with unprecedented complete selectivity. The reaction proceeds by two interlocked catalytic cycles comprising a radical chain reaction, which is initiated by visible light as energy source. This unorthodox synthetic strategy for the direct oxidative amination of alkyl groups has no biosynthetic precedence and provides an efficient and straightforward access to a general class of saturated nitrogenated heterocycles.

NOVEL ANTIVIRAL HELIOXANTHIN ANALOGS

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Page/Page column 40-41, (2010/02/14)

The present invention relates to novel antiviral helioxanthin analogs. These compounds may particularly be used alone or in combination with other drugs for the treatment of the following: hepadnaviruses, flaviviruses, herpesviruses and human immunodefici

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