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6-ethyl-1,4,5,7,8-pentahydroxynaphthalene-2,3-dione is a complex organic compound characterized by its unique molecular structure. It belongs to the class of naphthalene derivatives, which are known for their diverse applications in various industries. This particular compound features a naphthalene ring with five hydroxyl groups attached at positions 1, 4, 5, 7, and 8, and a carbonyl group at positions 2 and 3. The presence of an ethyl group at the 6th position further distinguishes it from other naphthalene derivatives. Due to its specific functional groups and structural features, 6-ethyl-1,4,5,7,8-pentahydroxynaphthalene-2,3-dione may exhibit unique chemical properties and reactivity, making it potentially useful in the synthesis of pharmaceuticals, dyes, or other specialty chemicals. However, its specific applications and properties would require further investigation and research to fully understand its potential uses and behavior in various chemical reactions.

1471-96-1

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1471-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1471-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1471-96:
(6*1)+(5*4)+(4*7)+(3*1)+(2*9)+(1*6)=81
81 % 10 = 1
So 1471-96-1 is a valid CAS Registry Number.

1471-96-1SDS

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-ethyl-1,4,5,7,8-pentahydroxynaphthalene-2,3-dione

1.2 Other means of identification

Product number -
Other names Echinochrome A

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:1471-96-1 SDS

1471-96-1Relevant academic research and scientific papers

DMSO-mediated transformation of 3-amino-2-hydroxynaphthazarins to natural 2,3-dihydroxynaphthazarins and related compounds

Polonik, Nikita S.,Polonik, Sergey G.

, p. 3303 - 3306 (2016)

A general and convenient method for the synthesis of naturally occurring and related hydroxylated naphthazarins has been developed. This protocol involves the oxidative DMSO-mediated transformation of 3-amino-2-hydroxynaphthazarins to 2,3-dihydroxynaphthazarins under acidic conditions. Based upon experimental observations, a plausible reaction mechanism is proposed.

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