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97860-59-8

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  • 1,4-Etheno-2,3-benzodioxin-1,4-dipropanoicacid, sodium salt (1:2)

    Cas No: 97860-59-8

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97860-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97860-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,6 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97860-59:
(7*9)+(6*7)+(5*8)+(4*6)+(3*0)+(2*5)+(1*9)=188
188 % 10 = 8
So 97860-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O6.2Na/c17-13(18)5-7-15-9-10-16(22-21-15,8-6-14(19)20)12-4-2-1-3-11(12)15;;/h1-4,9-10H,5-8H2,(H,17,18)(H,19,20);;

97860-59-8SDS

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 1,4-Etheno-2,3-benzodioxin-1,4-dipropanoic acid,disodium salt

1.2 Other means of identification

Product number -
Other names 3,3'-(1,4-Naphthylidene)dipropionate endoperoxide

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:97860-59-8 SDS

97860-59-8Relevant articles and documents

Is Water the Best or the Worst Solvent for Cycloadditions of Singlet Oxygen to Aromatic Compounds?

Cazin, Bernadette,Aubry, Jean-Marie,Rigaudy, Jean

, p. 952 - 953 (1986)

An accelerating effect of water, greater than two orders of magnitude, is observed for the photo-oxygenation of disodium 3,3'-(1,4-naphthylidene)dipropionate at variance with the current assumption on the constancy of the rate constant of 1O2 cycloadditions in various solvents.

Search for Singlet Oxygen in the Decomposition of Hydrogen Peroxide by Mineral Compounds in Aqueous Solutions

Aubry, J. M.

, p. 5844 - 5849 (2007/10/02)

The possibility of singlet oxygen (1O2) occurrence in the decomposition of H2O2 by mineral compounds in aqueous basic solutions was examined.Tetrapotassium rubrene-2,3,8,9-tetrcarboxylate was used as a trap, giving an endoperoxide detected by HPLC.We found that four families of mineral compounds lead to the formation of the endoperoxide: the oxides of the alkaline earths Ca, Sr, and Ba; the derivatives of elements of groups 3A, 4A, 5A, and 6A in d0 configuration (expect niobium); the oxides of actinides and lanthanides; and finally the oxidizers ClO-, BrO-, Au3+, IO3-, and IO4-.One compound in each family was selected for further investigation in order to strengthen the 1O2 hypothesis.Thus, the yield of the endoperoxide of potassium 9,10-diphenylanthracene-2,3,6,7-tetracarboxylate was enhanced when the parent compound was introduced in a mixture of H2O2 + (ClO-, Nd2O3, MoO42-, Ca(OH)2 + deuterated water instead of light water.

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