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1H,3H-Naphthol[1,8-cd]pyran-1,3dione,6-methoxy- is a complex organic compound with the chemical formula C13H8O4. It is a derivative of naphthalene, featuring a pyran ring fused to the naphthalene core. The compound is characterized by the presence of two carbonyl groups (C=O) at positions 1 and 3, and a methoxy group (-OCH3) at position 6. This molecule is known for its unique chemical structure and potential applications in various fields, such as pharmaceuticals and materials science. Due to its specific arrangement of functional groups, it may exhibit distinct chemical properties and reactivity compared to other naphthalene derivatives.

17190-36-2

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17190-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17190-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17190-36:
(7*1)+(6*7)+(5*1)+(4*9)+(3*0)+(2*3)+(1*6)=102
102 % 10 = 2
So 17190-36-2 is a valid CAS Registry Number.

17190-36-2SDS

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-naphtho[1,8-cd]pyran-1,3-dione

1.2 Other means of identification

Product number -
Other names 4-methoxy-naphthalene-1,8-dicarboxylic acid anhydride

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:17190-36-2 SDS

17190-36-2Relevant academic research and scientific papers

1,2-Derivatives of Acenaphthylene. XIV. Synthesis and Methoxydehalogenation of Acetals of 5-Halo-1,2-Acenaphthenediones

Anikin,Samburskii,Mazepa

, p. 234 - 238 (2007/10/03)

On heating 5-bromo or 5-chloro-1,2-acenaphthenediones with 2,2-dimethylpropanediol under conditions of acid catalysis the former compound does not afford acetals of both carbonyls but only a mixture of isomeric acetals of a single carbonyl. Under treatment of the individual above acetals with sodium methoxide the five-membered cycle is retained, and methoxydehalogenation occurs with the isomer containing halogen in para-position with respect to carbonyl group.

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