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6-Amino-5,6,7,8-tetrahydro-1-naphthalenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75016-98-7

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75016-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75016-98-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75016-98:
(7*7)+(6*5)+(5*0)+(4*1)+(3*6)+(2*9)+(1*8)=127
127 % 10 = 7
So 75016-98-7 is a valid CAS Registry Number.

75016-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-OH-AT

1.2 Other means of identification

Product number -
Other names 5,6,7,8-tetrahydro-6-amino-1-naphthol

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:75016-98-7 SDS

75016-98-7Downstream Products

75016-98-7Relevant academic research and scientific papers

Affinity for dopamine D2, D3, and D4 receptors of 2-aminotetralins. Relevance of D2 agonist binding for determination of receptor subtype selectivity.

van Vliet,Tepper,Dijkstra,Damsma,Wikstroem,Pugsley,Akunne,Heffner,Glase,Wise

, p. 4233 - 4237 (2007/10/03)

A series of 2-aminotetralins, substituted with a methoxy or a hydroxy group on the 5- or 7-position, and with varying N-alkyl or N-arylalkyl substituents, were prepared and evaluated in binding assays for human dopamine (DA) D2, D3, and D4 receptors. Some members of this series were prepared in former studies, but were never tested in vitro with single receptor subtypes, and these were examined again. None of the tested 2-aminotetralins showed high affinity for the dopamine D4 receptor. However, a number of the 2-aminotetralins showed high affinity for both the D2 and the D3 DA receptors, as exemplified by compounds 11-15 and 21-26, while some had a reasonable selectivity for the DA D3 receptors. The affinities of the 2-aminotetralins for the D21, receptor depended on the type of radioligand (agonist or antagonist) used. The agonist affinity data, obtained by using the agonist ligand [3H]N-0437, are thought to be more relevant for calculating DA receptor subtype selectivity.

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