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156731-04-3

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156731-04-3 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 156731-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,3 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 156731-04:
(8*1)+(7*5)+(6*6)+(5*7)+(4*3)+(3*1)+(2*0)+(1*4)=133
133 % 10 = 3
So 156731-04-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H21NO4/c1-12-10-11-2-4-13-6-8-15-9-7-14-5-3-11/h2-10H2,1H3/p+1

156731-04-3SDS

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 N-(methoxymethyl)-1,4,7-trioxa-10-azacyclododecane

1.2 Other means of identification

Product number -
Other names N-METHOXYMETHYLAZA-12-CROWN-4

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 -
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More Details:156731-04-3 SDS

156731-04-3Downstream Products

156731-04-3Relevant articles and documents

Molecular structure of novel polymer-like complexes of armed-azacrown ethers with alkali-metal cations

Habata, Yoichi,Akabori, Sadatoshi

, p. 3871 - 3882 (2007/10/03)

Armed-azacrown ethers N,N′-bis(4-hydroxy-3,5-dimethylbenzyl)-1,4,10,13-tetraoxa-7,16- diazacyclooctadecane 1, N-(4-hydroxy-3,5-dimethylbenzyl)-1,4,7,10-tetraoxa-13-azacyclopentadecane 2 and -1,4,7-trioxa-10-azacyclododecane 3, and their alkali-metal complexes were prepared. Single crystal structures have been determined for 1, 1·KI·3H2O, 1·KSCN·H2O, 2·NaSCN, 2·KSCN, 2·RbSCN and 2·CsSCN, 3, 3·LiSCN·H2O, 3·LiBr·3H2O and 3·RbSCN. The compounds 1·KI·3H2O and 1·KSCN·H2O are normal 1:1 complexes, but 2·NaSCN, 2·KSCN, 2·RbSCN and 2·CsSCN are novel polymer-like (1:1) complexes in which the phenolic OH group in the side arm of the crown ether co-ordinates to the cation incorporated in the crown moiety of another molecule. In the complexes of 3, when Li+ is used as guest cation, the normal 1:1 complex is obtained, but Rb+ forms a polymer-like (2: 2)n complex. Fourier-transform IR spectra showed that the O-H stretching band of the phenolic OH group in the polymer-like complexes shifted to lower frequency by ca. 210-290 cm-1 compared with those of the corresponding host compounds. Also, 13C NMR titration experiments indicated that the stoichiometry of the alkali-metal complexes with 2 and 3 in CD3CN-CD3OD (5:1) solution is 1:1, and thus they do not form polymer-like complexes under these conditions.

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