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3-Dibenzofurancarbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51818-91-8

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51818-91-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51818-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,1 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51818-91:
(7*5)+(6*1)+(5*8)+(4*1)+(3*8)+(2*9)+(1*1)=128
128 % 10 = 8
So 51818-91-8 is a valid CAS Registry Number.

51818-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dibenzofuran-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-Dibenzofurancarboxaldehyde

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:51818-91-8 SDS

51818-91-8Relevant academic research and scientific papers

N-(2-ARYLETHYL) BENZYLAMINES AS ANTAGONISTS OF THE 5-HT6 RECEPTOR

-

Paragraph 0142, (2016/01/25)

The present invention relates to the use compounds of formula I which are antagonists of the 5-HT 6 receptor, for treating a cognitive disorder selected from the group consisting of age-related cognitive decline, mild cognitive impairment and dementia

Synthesis of Dibenzofurans via C-H Activation of o-Iodo Diaryl Ethers

Panda, Niranjan,Mattan, Irshad,Nayak, Dinesh Kumar

, p. 6590 - 6597 (2015/10/06)

An efficient method for the synthesis of dibenzofuran from o-iododiaryl ether using reusable Pd/C under ligand-free conditions has been developed. Synthesis of o-iododiaryl ether was achieved in one pot through sequential iodination and O-arylation of phenol under mild reaction conditions.

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