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3,4,6,7,9,10,12,13-Octahydro-2,5,8,11,14-benzopentaoxacycloheptadecin-1,15-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21161-08-0

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21161-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21161-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,1,6 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21161-08:
(7*2)+(6*1)+(5*1)+(4*6)+(3*1)+(2*0)+(1*8)=60
60 % 10 = 0
So 21161-08-0 is a valid CAS Registry Number.

21161-08-0SDS

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 3,4,6,7,9,10,12,13-octahydro-2,5,8,11,14-benzopentaoxacycloheptadecine-1,15-dione

1.2 Other means of identification

Product number -
Other names benzo-[o]-1,4,7,10,13-pentaoxacycloheptadecane-14,17-dione

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:21161-08-0 SDS

21161-08-0Downstream Products

21161-08-0Relevant academic research and scientific papers

A convenient synthesis of new macrocyclic thioether-esters and ether-esters: Extraction properties of these esters for alkali, alkaline earth, and transition metal cations

Seyedi, Seyed Mohammad,Shadkam,Ziafati

, p. 1953 - 1960 (2007/10/03)

Macrocyclic thioether-esters and ether-esters have been prepared by treating 2,2′-dithiobenzoic acid dichloride and 1,2-benzendicarboxylic acid dichloride with appropriate glycols or dithiol. The complexing ability of these thioether-esters and ether-esters toward Li+, Na+, K+, Mg2+, Ca2+, Sr2+, Ba 2+, Co2+, and Ni2+ has been measured by the solvent extraction method. The extraction data indicate that compound 2 exhibits stronger selectivity toward Li+, 3 toward Ba2+, 4 toward K+, 5 toward Mg2+, 6 toward Ba2+ and Sr 2+, and 7 toward Co2+ and Ni2+ when compared with other cations. Copyright Taylor & Francis Inc.

Synthesis of macrocyclic polyether-diester compounds using Al2O3/MeSO3H (AMA) as a new reagent

Sharghi, Hashem,Sarvari, Mona Hosseini

, p. 879 - 882 (2007/10/03)

A new simple and convenient method for the synthesis of macrocyclic polyether-diester compounds containing pyridine and phenyl subcyclic units is developed. Various diacids, are selectively esterified in excellent yields by reaction with oligoethylene glycols in the presence of Al2O3/MeSO3H (AMA) as a new reagent without use of any solvents.

Tris(2-methoxyphenyl)bismuthane as a Dehydrating Agent with High Template Ability: an Efficient Single-step Synthesis of Macrocyclic Diesters from Diacid Anhydrides and Glycols

Ogawa, Takuji,Yoshikawa, Akemi,Wada, Hidemi,Ogawa, Chie,Ono, Noboru,Suzuki, Hitomi

, p. 1407 - 1408 (2007/10/02)

Tris(2-methoxyphenyl)bismuthane works as both a mild dehydrating agent and a good template for macrocyclic ester synthesis; prolonged heating of the bismuthane with a dicarboxylic acid anhydride and a glycol in toluene under reflux afforded the corresponding macrocyclic 1:1 diester in moderate to good yields, together with a small amount of a macrocyclic 2:2 tetraester.

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