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1,6-Dimethoxy-dibenzo[1,4]dioxin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27974-34-1

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27974-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27974-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,7 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27974-34:
(7*2)+(6*7)+(5*9)+(4*7)+(3*4)+(2*3)+(1*4)=151
151 % 10 = 1
So 27974-34-1 is a valid CAS Registry Number.

27974-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Dimethoxy-dibenzo[1,4]dioxin

1.2 Other means of identification

Product number -
Other names 1,6-Dimethoxy-dibenzo-p-dioxin

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:27974-34-1 SDS

27974-34-1Relevant academic research and scientific papers

Photolysis of bis(methoxyphenyl) methylphosphonates. Their emission spectra and formation of dimethoxybiphenyl and dimethoxy-9,10-dioxaanthracene

Shi, Min,Okamoto, Yoshiki,Takamuku, Setsuo

, p. 6899 - 6902 (2007/10/02)

Upon UV-irradiation in methanol, bis(methoxyphenyl) methylphosphonates underwent an intramolecular coupling of two methoxyphenyl groups to give dimethoxybiphenyls and dimethoxy-9,10-dioxaanthracenes. The reactivities and fluorescence spectra of the phosphonates were sensitive to the position of the methoxy group. These photo-induced couplings proceed probably through the formation of the two types of singlet intramolecular excimers.

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