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22246-26-0

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22246-26-0 Usage

General Description

6-Nitro-1-tetralone is a chemical compound with the molecular formula C10H9NO3. It is a yellow crystalline solid with a nitro group attached to the 6th position of the tetralone ring. 6-Nitro-1-tetralone is used in organic synthesis and medicinal chemistry as a building block for various pharmaceuticals and agrochemicals. It has also been studied for its potential pharmacological properties, including its effects on the central nervous system. However, it is important to handle this compound with care due to its potential hazards, including being harmful if swallowed, inhaled, or in contact with skin, and its ability to cause skin and eye irritation.

Check Digit Verification of cas no

The CAS Registry Mumber 22246-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,4 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22246-26:
(7*2)+(6*2)+(5*2)+(4*4)+(3*6)+(2*2)+(1*6)=80
80 % 10 = 0
So 22246-26-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO3/c12-10-3-1-2-7-6-8(11(13)14)4-5-9(7)10/h4-6H,1-3H2

22246-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-nitro-3,4-dihydro-2H-naphthalen-1-one

1.2 Other means of identification

Product number -
Other names 6-Nitro-tetralon-(1)

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:22246-26-0 SDS

22246-26-0Relevant articles and documents

One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl- protected amines from ketones

Tanuwidjaja, Jessica,Peltier, Hillary M.,Ellman, Jonathan A.

, p. 626 - 629 (2007/10/03)

A one-pot method for the asymmetric synthesis of tert-butanesulfinyl- protected amines is described. Condensation of aryl alkyl and dialkyl ketones with tert-butanesulfinamide followed by in situ reduction with the appropriate reagent provides either dias

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