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1,4-Naphthalenedione, 2,3-dihydro-2,3-dihydroxy-, cis- is a chemical compound with the molecular formula C10H8O4. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and is characterized by the presence of two hydroxyl groups (-OH) attached to the 2,3-dihydro-2,3-dihydroxy structure. The cis- configuration indicates that the hydroxyl groups are positioned on the same side of the molecule. 1,4-Naphthalenedione, 2,3-dihydro-2,3-dihydroxy-, cis- is also known as cis-2,3-dihydroxy-1,4-naphthoquinone and has potential applications in various fields, including pharmaceuticals and organic synthesis. It is important to note that the compound's properties, such as solubility and reactivity, may vary depending on its specific form and the conditions under which it is used.

34785-82-5

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34785-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34785-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,8 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34785-82:
(7*3)+(6*4)+(5*7)+(4*8)+(3*5)+(2*8)+(1*2)=145
145 % 10 = 5
So 34785-82-5 is a valid CAS Registry Number.

34785-82-5SDS

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 dihydrodihydroxynaphthoquinone

1.2 Other means of identification

Product number -
Other names 2,3-Dihydroxy-2,3-dihydro-naphthochinon-(1,4)

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:34785-82-5 SDS

34785-82-5Upstream product

34785-82-5Downstream Products

34785-82-5Relevant academic research and scientific papers

Dimethyldioxirane oxidation of hydroquinones into quinones and 2,3-dihydroxycyclohexene-1,4-diones

Adam,Schonberger

, p. 53 - 56 (1992)

Dehydrogenation of hydroquinones 1 by dimethyldioxirane affords quinones 2 and oxygen transfer the novel 2,3-dihydroxycyclohexene-1,4-diones 3; an electron transfer mechanism is proposed for these oxidations.

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