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2-[(2-methylpropyl)amino]naphthalene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92248-18-5

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92248-18-5 Usage

Substituent

2-methylpropylamine

Applications

fluorescent probe for cell detection, potential therapeutic agent

Unique structure and properties

subject of scientific research in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 92248-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 92248-18:
(7*9)+(6*2)+(5*2)+(4*4)+(3*8)+(2*1)+(1*8)=135
135 % 10 = 5
So 92248-18-5 is a valid CAS Registry Number.

92248-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylpropylamino)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2-isobutylamino-1,4-naphthoquinone

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:92248-18-5 SDS

92248-18-5Downstream Products

92248-18-5Relevant academic research and scientific papers

Synthesis of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones

Gornostaev,Kryukovskaya,Lavrikova,Vigant,Gatilov, Yu. V.

, p. 205 - 210 (2014/04/17)

The reaction of 2-amino(alkylamino)-1,4-naphthoquinones with nitrating mixture in concentrated sulfuric acid leads to the formation of 2-amino(alkylamino)-3-nitro-1,4-naphthoquinones.

Naphthoquinone-directed C-H annulation and Csp3-H bond cleavage: One-pot synthesis of tetracyclic naphthoxazoles

Wang, Meining,Zhang, Chi,Sun, Li-Ping,Ding, Chunyong,Zhang, Ao

, p. 4553 - 4560 (2014/06/09)

One-pot synthesis of tetracyclic naphthoxazole derivatives from electron-deficient naphthoquinones and alkynes was achieved via Rh(III)-catalyzed C-H activation and Csp3-H bond cleavage for the first time. This approach proceeds through a tandem cascade process involving substrate tautomerization, C-H activation, oxidative addition, cyclization, and aromatization. In addition, broad substrate scope, simple starting materials, and steric tolerance make this strategy of great practicality.

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