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1,4-Naphthalenedione, 7-acetyl-8-hydroxy-2-methoxy-6-methyl- is a complex organic compound with the chemical formula C14H12O5. It is a derivative of naphthalene, a two-ring aromatic hydrocarbon, with specific functional groups attached to it. The compound features a 1,4-naphthoquinone core, which is a type of quinone with two carbonyl groups at the 1 and 4 positions. Additionally, it has an acetyl group (-COCH3) at the 7 position, a hydroxyl group (-OH) at the 8 position, a methoxy group (-OCH3) at the 2 position, and a methyl group (-CH3) at the 6 position. This chemical structure endows the compound with unique properties and potential applications in various fields, such as pharmaceuticals, dyes, and materials science.

64756-97-4

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64756-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64756-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64756-97:
(7*6)+(6*4)+(5*7)+(4*5)+(3*6)+(2*9)+(1*7)=164
164 % 10 = 4
So 64756-97-4 is a valid CAS Registry Number.

64756-97-4SDS

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-acetyl-5-hydroxy-3-methoxy-7-methylnaphthoquinone

1.2 Other means of identification

Product number -
Other names 7-Acetyl-8-hydroxy-2-methoxy-6-methyl-[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:64756-97-4 SDS

64756-97-4Upstream product

64756-97-4Downstream Products

64756-97-4Relevant academic research and scientific papers

REGIOSPECIFIC FRIEDEL-CRAFTS ACYLATION OF 6-ALKOXY-2-PYRONES:PREPARATION OF SUBSTITUTED AROMATICS AND ANTHRAQUINONES.

Jung, Michael E.,Brown, Richard W.

, p. 3355 - 3358 (2007/10/02)

Friedel-Crafts acylation of 6-alkoxy-2-pyrones gives high yields of the 5-acyl-2-pyrones which undergo regioselective cycloaddition with various dienophiles.

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