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2-Naphthalenol, 8-nitro- is an organic compound with the chemical formula C10H7NO3. It is a yellow crystalline solid that is derived from naphthalene, a polycyclic aromatic hydrocarbon. 2-Naphthalenol, 8-nitro- is characterized by the presence of a hydroxyl group (-OH) at the 2-position and a nitro group (-NO2) at the 8-position on the naphthalene ring. 2-Naphthalenol, 8-nitro- is used in the synthesis of dyes and pharmaceuticals, and it is also known for its potential applications in the field of materials science. Due to its chemical structure, it exhibits certain properties such as low solubility in water and high solubility in organic solvents. It is important to handle 2-Naphthalenol, 8-nitro- with care, as it may have toxic effects and should be stored away from heat and open flames.

607-39-6

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607-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607-39-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 607-39:
(5*6)+(4*0)+(3*7)+(2*3)+(1*9)=66
66 % 10 = 6
So 607-39-6 is a valid CAS Registry Number.

607-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-nitronaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 2-Naphthalenol, 8-nitro-

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:607-39-6 SDS

607-39-6Upstream product

607-39-6Relevant academic research and scientific papers

Hydroxylation of nitrated naphthalenes with KO2/crown ether

Fukuhara,Hara,Nakanishi,Miyata

, p. 1532 - 1535 (2000)

Superoxide radical anion (O2/·-), generated by KO2/crown ether, is effective for hydroxylation of nitronaphthalenes. When mono- and di-nitronaphthalenes are treated with KO2/crown ether, hydroxylation results at

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