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82572-03-0

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82572-03-0 Usage

General Description

(R)-1-(Naphthalen-2-yl)ethanamine hydrochloride is a chemical compound that belongs to the class of aryl ethylamines. It is a salt form of the amine compound and is commonly used in pharmaceutical research and drug development. (R)-1-(Naphthalen-2-yl)ethanamine hydrochloride has potential biological activities and is often studied for its potential use in the treatment of various neurological and psychiatric disorders. It is also used as a chemical intermediate in the synthesis of various organic compounds. Additionally, (R)-1-(Naphthalen-2-yl)ethanamine hydrochloride is known for its ability to act as a selective agonist for certain receptors in the central nervous system, making it an important compound in neuroscience research.

Check Digit Verification of cas no

The CAS Registry Mumber 82572-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82572-03:
(7*8)+(6*2)+(5*5)+(4*7)+(3*2)+(2*0)+(1*3)=130
130 % 10 = 0
So 82572-03-0 is a valid CAS Registry Number.

82572-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Naphthalenemethanamine, α-methyl-, hydrochloride (), (αR)-

1.2 Other means of identification

Product number -
Other names 2-Naphthalenemethanamine, α-methyl-, hydrochloride, (R)-

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:82572-03-0 SDS

82572-03-0Downstream Products

82572-03-0Relevant articles and documents

Iridium/monodentate phosphoramidite catalyzed asymmetric hydrogenation of N-aryl imines

Mrsic, Natasa,Minnaard, Adriaan J.,Feringa, Ben L.,Vries, Johannes G. de

supporting information; experimental part, p. 8358 - 8359 (2009/10/23)

(Chemical Equation Presented) Asymmetric hydrogenation of N-aryl acetophenone imines using iridium/PipPhos leads to very high enantioselectivities up to >99percent depending on the presence of electron-donating substituents in the 2-, 3-, and 5-position of the aryl ring. If the substituent is 2-methoxy, the resultant secondary amines are easily oxidatively deprotected using trichloroisocyanuric acid to give the primary amines ingood yield with full retention of enantioselectivity.

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