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1,2-Benzenediol,3-(2,6-dihydroxy-4-methylphenoxy)- 5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81827-49-8

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81827-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81827-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,2 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81827-49:
(7*8)+(6*1)+(5*8)+(4*2)+(3*7)+(2*4)+(1*9)=148
148 % 10 = 8
So 81827-49-8 is a valid CAS Registry Number.

81827-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name violacerol-II

1.2 Other means of identification

Product number -
Other names violaceol-II

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:81827-49-8 SDS

81827-49-8Relevant academic research and scientific papers

Phenyl ethers from cultured lichen mycobionts of Graphis scripta var. serpentina and G. rikuzensis.

Takenaka, Yukiko,Tanahashi, Takao,Nagakura, Naotaka,Hamada, Nobuo

, p. 794 - 797 (2007/10/03)

Spore-derived mycobionts of the lichen Graphis scripta var. serpentina and G. rikuzensis were cultivated on a malt-yeast extract medium supplemented with 10% sucrose and their metabolites were investigated. 3,3'-Dihydroxy-5,5'-dimethyldiphenyl ether was isolated from the cultures of the mycobionts of G. scripta var. serpentina, while a new phenyl ether, rikuzenol, along with two known diphenyl ethers, violaceol-I and violaceol-II, were isolated from those of G. rikuzensis. The structure of the new compound was determined by spectroscopic methods. Violaceol-I was chemically synthesized and interconversion between violaceol-I and violaceol-II was proven.

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