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5,6,7,8-tetrahydronaphthalene-1,4-diyl diacetate is a chemical compound with the molecular formula C12H14O4. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, where four hydrogen atoms are added to the molecule, resulting in a tetracyclic structure. The compound features two acetate groups attached to the 1 and 4 positions of the naphthalene ring, which are esterified to the hydroxyl groups. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and other chemical products. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest in organic chemistry research and development.

7475-24-3

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7475-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7475-24-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7475-24:
(6*7)+(5*4)+(4*7)+(3*5)+(2*2)+(1*4)=113
113 % 10 = 3
So 7475-24-3 is a valid CAS Registry Number.

7475-24-3SDS

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 (4-acetyloxy-5,6,7,8-tetrahydronaphthalen-1-yl) acetate

1.2 Other means of identification

Product number -
Other names 5.8-Diacetoxy-tetralin

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:7475-24-3 SDS

7475-24-3Relevant academic research and scientific papers

Efficient ortho-oxidation of phenols with diacyl peroxides

Tada, Masahiro,Ishiguro, Risa,Izumi, Ryohei

, p. 239 - 242 (2008/09/21)

A stable symmetric diacyl peroxide, m-chlorobenzoyl peroxide (mCBPO), and an asymmetric diacyl peroxide, chloroacetyl m-chlorobenzoyl peroxide (CAMCBPO), were synthesized from m-chloroperbenzoic acid. Both peroxides oxidized phenols selectively at the ortho position predoninantly. CAMCBPO gave para-oxidized compounds as minor products from some phenols. The improvement of the yield of ortho-oxidation of phenols with mCBPO was also reported.

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