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75265-05-3

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75265-05-3 Usage

Molecular structure

Consists of a naphthalene ring with a naphthoquinone group and an epoxide functional group attached.

Type of compound

Synthetic organic compound.

Potential uses

Has been studied for its potential use in the treatment of various diseases and as a precursor in the synthesis of other bioactive compounds.

Therapeutic potential

Has shown potential as an antiviral agent and has been investigated for its potential anticancer properties.

Unique characteristics

Its unique structure and reactivity make it an interesting target for further research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 75265-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75265-05:
(7*7)+(6*5)+(5*2)+(4*6)+(3*5)+(2*0)+(1*5)=133
133 % 10 = 3
So 75265-05-3 is a valid CAS Registry Number.

75265-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(oxiran-2-yl)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names -

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:75265-05-3 SDS

75265-05-3Downstream Products

75265-05-3Relevant articles and documents

SYNTHESIS OF OXIRANYLQUIONOES AS NEW POTENTIAL BIOREDUCTIVE ALKYLATING AGENTS

Syper L.,Mlochowsky, J.,Kloc, K.

, p. 781 - 792 (2007/10/02)

1,4-Benzoquinones and 1,4-naphtoquinones carrying oxiranyl substituents have been synthesized as potential bioreductive alkylating agents.The method presented here involves the syntheses of 1,4-dimethoxybenzaldehydes or 1,4-dimethoxynaphtaldehydes, and co

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