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81861-30-5

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81861-30-5 Usage

General Description

6-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-ylamine is a chemical compound with the molecular formula C11H15NO. It is an amine derivative and belongs to the class of organic compounds known as arylamines, which are organic compounds containing an amine group attached to an aromatic ring. 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-ylamine has a tetrahydro-naphthalene backbone, with a methoxy group attached to it. It is commonly used in medicinal chemistry, particularly in the development of pharmaceutical drugs. 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-ylamine has potential applications in the treatment of various medical conditions, and its chemical properties make it a valuable tool for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 81861-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81861-30:
(7*8)+(6*1)+(5*8)+(4*6)+(3*1)+(2*3)+(1*0)=135
135 % 10 = 5
So 81861-30-5 is a valid CAS Registry Number.

81861-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-1,2,3,4-tetrahydronaphthalen-2-amine

1.2 Other means of identification

Product number -
Other names 2-amino-6-methoxytetralin

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:81861-30-5 SDS

81861-30-5Relevant articles and documents

INDOLE AHR INHIBITORS AND USES THEREOF

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Paragraph 00587; 00589, (2018/11/22)

The present invention provides compounds useful as inhibitors of AHR, compositions thereof, and methods of using the same.

Artificial multi-enzyme networks for the asymmetric amination of sec-alcohols

Tauber, Katharina,Fuchs, Michael,Sattler, Johann H.,Pitzer, Julia,Pressnitz, Desiree,Koszelewski, Dominik,Faber, Kurt,Pfeffer, Jan,Haas, Thomas,Kroutil, Wolfgang

, p. 4030 - 4035 (2013/04/10)

Various artificial network designs that involve biocatalysts were tested for the asymmetric amination of sec-alcohols to the corresponding α-chiral primary amines. The artificial systems tested involved three to five redox enzymes and were exemplary of a range of different sec-alcohol substrates. Alcohols were oxidised to the corresponding ketone by an alcohol dehydrogenase. The ketones were subsequently aminated by employing a ω-transaminase. Of special interest were redox-neutral designs in which the hydride abstracted in the oxidation step was reused in the amination step of the cascade. Under optimised conditions up to 91 % conversion of an alcohol to the amine was achieved. Trickle-down effect: The asymmetric amination of sec-alcohols to the corresponding α-chiral primary amines was performed with a biocatalytic cascade whereby the various steps were interconnected through the cofactors/cosubstrates. In a redox-neutral cascade and under optimised conditions, up to 91 % conversion of an alcohol to the amine was achieved. Copyright

SUBSTITUTED TETRALINS AND INDANES AND THEIR USE

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Page 31, (2008/06/13)

This invention features tetralin and indane compounds, compositions containing them, and methods of using them as PPAR alpha modulators to treat or inhibit the progression of, for example, diabetes.

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