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88548-60-1

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88548-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88548-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,4 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88548-60:
(7*8)+(6*8)+(5*5)+(4*4)+(3*8)+(2*6)+(1*0)=181
181 % 10 = 1
So 88548-60-1 is a valid CAS Registry Number.

88548-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 13-[(4-nitrophenyl)methyl]-1,4,7,10-tetraoxa-13-azacyclopentadecane

1.2 Other means of identification

Product number -
Other names 1,4,7,10-Tetraoxa-13-azacyclopentadecane,13-[(4-nitrophenyl)methyl]

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:88548-60-1 SDS

88548-60-1Downstream Products

88548-60-1Relevant articles and documents

Synthesis and complex-forming properties of N-substituted diazacrown ethers

Luk'yanenko,Basok,Kulygina,Vetrogon

, p. 1919 - 1924 (2007/10/03)

N-Substituted mono- and diazacrown ether with ethoxycarbonylmethyl, 7-phenyl-3,6-dioxaheptyl, p-methoxy, and p-nitrobenzyl groups in the side chain have been synthesized. Their reactions with alkali and alkaline-earth metals have been studied. Substituent

Direct ESR Evidence for Sodium Selective, Intramolecular Ion Pairing in Redox-Switched Nitrogen-Pivot Lariat Ethers

Delgado, Milagros,Echegoyen, Luis,Gatto, Vincent J.,Gustowski, Deborah A.,Gokel, George W.

, p. 4135 - 4138 (2007/10/02)

N-(2-Nitrobenzyl)aza-15-crown-5, 1, and the sidearm hexadeuterio analogue 2 have been reduced electrochemically to their corresponding radical anion forms and analyzed by ESR.Addition of Li(1+), Na(1+), or K(1+) to the solutions leads to changes in the ESR spectra but the changes are most marked when Na(1+) is present.Essentially no change is observed in the ESR spectrum of 2-nitrotoluene, confirming that both macroring and sidearm must be involved for the intramolecular ion pair to be stable.The radical anion sidearm compexes must be relatively rigid species since the strongest sidearm interaction is observed with Na(1+) cation which is closest in size to the cavity formed by the cooperating macroring and sidearm.

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