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810676-31-4

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810676-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 810676-31-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,0,6,7 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 810676-31:
(8*8)+(7*1)+(6*0)+(5*6)+(4*7)+(3*6)+(2*3)+(1*1)=154
154 % 10 = 4
So 810676-31-4 is a valid CAS Registry Number.

810676-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 7,8-dihydroxy-2-oxochromene-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 7,8-dihydroxy-2-oxo-2H-chromene-3-carboxylate

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:810676-31-4 SDS

810676-31-4Downstream Products

810676-31-4Relevant articles and documents

Synthesis and structure-activity relationship of daphnetin derivatives as potent antioxidant agents

Xia, Yangliu,Chen, Chen,Liu, Yong,Ge, Guangbo,Dou, Tongyi,Wang, Ping

supporting information, (2018/10/05)

In this study, daphnetin 1 was chosen as the lead compound, and C-3 or C-4-substituted daphnetins were designed and synthesized to explore the potential relationship between the antioxidant activities and the chemical structures of daphnetin derivatives. The antioxidant activities of the generated compounds were evaluated utilizing the free radical scavenging effect on 2,2-diphenyl-1-picrylhydrazyl, 2,2-azinobis-(3-ethylbenzthiazoline-6-sulfonate) cation, and the ferric reducing power assays, and were then compared with those of the standard antioxidant Trolox. The results showed that the catechol group was the key pharmacophore for the antioxidant activity of the daphnetins. The introduction of an electron-withdrawing hydrophilic group at the C-4 position of daphnetin enhanced the antioxidative capacity, but this trend was not observed for C-3 substitution. In addition, introduction of a a hydrophobic phenyl group exerted negative effects on the antioxidant activity in both the C-3 and C-4 substitutions. Among all of the derivatives tested, the most powerful antioxidant was 4-carboxymethyl daphnetin (compound 9), for which the strongest antioxidant activity was observed in all of the assays. In addition, compound 9 also displayed strong pharmaceutical properties in the form of metabolic stability. To summarize, compound 9 holds great potential to be developed as an antioxidant agent with excellent antioxidant activity and proper pharmacokinetic behavior.

New green, recyclable magnetic nanoparticles supported amino acids as simple heterogeneous catalysts for knoevenagel condensation

Girija,Naik, H.S. Bhojya,Kumar, B. Vinay,Sudhamani,Harish

, p. 468 - 477 (2013/08/23)

Coumarin derivatives were synthesized using magnetically recoverable iron oxide nanoparticles supported amino acids as heterogeneous catalysts via one-pot multi component reaction using MW irradiation. Easy recovery of the catalyst using an external magne

ZnO/MgO Containing ZnO Nanoparticles as a Highly Effective Heterogeneous Base Catalyst for the Synthesis of 4H-Pyrans and Coumarins in [bmim]BF 4

Valizadeh,Azimi

experimental part, p. 123 - 130 (2012/01/03)

4H-Pyrans and coumarins were synthesized through one-pot reactions using ZnO/MgO solid sample containing ZnO nanoparticles as an efficient reusable catalyst in ionic liquid, [bmim]BF4. The catalyst is inexpensive and readily available, stable and storable

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