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6,6'-Methylenebis-1,3-benzodioxol-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78188-48-4

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78188-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78188-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,8 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78188-48:
(7*7)+(6*8)+(5*1)+(4*8)+(3*8)+(2*4)+(1*8)=174
174 % 10 = 4
So 78188-48-4 is a valid CAS Registry Number.

78188-48-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[(6-hydroxy-1,3-benzodioxol-5-yl)methyl]-1,3-benzodioxol-5-ol

1.2 Other means of identification

Product number -
Other names 6,6'-Methylenebis-1,3-benzodioxol-5-ol

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:78188-48-4 SDS

78188-48-4Downstream Products

78188-48-4Relevant academic research and scientific papers

Preparation of 2,2'-dihydroxytriphenylmethanes using metal phenolates with aromatic aldehydes

Mibu,Sumoto

, p. 1810 - 1813 (2000)

The reactions of oxophilic metal phenolates having electron-donating substituents (1a-c) with aromatic aldehydes (2, 3) were selectively condensed at the ortho-position of the starting phenol to afford 2,2'-dihydroxytriphenylmethanes (8-11). This method w

Synthesis and Antioxidant Capacity of Some Derivatives of Sesamol at the C-6 Position

Buravlev, Evgeny V.,Shevchenko, Oksana G.,Suponitsky, Kyrill Yu.

, (2021/05/27)

Several synthetic approaches (aminomethylation, alkylation, condensation, etc.) have been used to synthesize derivatives based on the sesamol (1), natural phenol. The set of methods, including the study of antioxidant activity (AOA) by the ability to inhibit the initiated oxidation of animal lipids, radical scavenging activity, Fe2+-chelation ability, as well as a comparative assessment of membrane-protective activity under the conditions of H2O2-induced hemolysis of mice red blood cells (RBCs), was used to analyze the antioxidant potential of the synthesized compounds. The synthesized derivatives have demonstrated different activity in the listed test systems, and we have identified compounds which appear to be most promising for a detailed study of their pharmacological properties.

Identification of sesamol byproducts produced by plasma treatment with inhibition of advanced glycation endproducts formation and ONOO? scavenging activities

Jeong, Gyeong Han,Jeong, Yong-Ha,Jeong, Yun Hee,Kim, Tae Hoon

, (2020/01/21)

Little is known of plasma-mediated relations between major food components and their biological capacities. In the present work, the effects of dielectric barrier discharge (DBD) plasma irradiation on pure sesamol and sesame oil were investigated using sp

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