ChemicalBook >> CAS DataBase List >>4',4''(5'')-Di-tert-butyldibenzo-18-crown-6

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6

CAS No.
29471-17-8
Chemical Name:
4',4''(5'')-Di-tert-butyldibenzo-18-crown-6
Synonyms
Di-(tert-butylbenzo)-18-crown-6;Bis(tert-butylbenzo)-18-crown-6;4,4'-Di-tert-butyldibenzo-18-crown-6;14)-bis(1,1-dimethylethyl)-ro-13(or2;AR,AR'-DI-TERT-BUTYLDIBENZO-18-CROWN-6;4',4''(5'')-DI-TERT-BUTYLDIBENZO-18-CROWN-6;4',4pi(5pi)-Di-tert-butyldibenzo-18-crown-6;4',4''(5'')-DI-TERT-BUTYLDIBENZO-18-CROWN-6;4',4''(5'')-Di-tert-butyldibenzo-18-crown-6,94%;4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 95%
CBNumber:
CB7722219
Molecular Formula:
C28H40O6
Molecular Weight:
472.61
MDL Number:
MFCD00068541
MOL File:
29471-17-8.mol
MSDS File:
SDS
Last updated:2024-04-25 14:22:04

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 Properties

Melting point 112-116 °C
Boiling point 533.38°C (rough estimate)
Density 1.0542 (rough estimate)
refractive index 1.6000 (estimate)
BRN 1667522
InChI InChI=1S/C28H40O6/c1-27(2,3)21-7-9-23-25(19-21)33-17-13-30-14-18-34-26-20-22(28(4,5)6)8-10-24(26)32-16-12-29-11-15-31-23/h7-10,19-20H,11-18H2,1-6H3
InChIKey CVQLBTRJDFZYMS-UHFFFAOYSA-N
SMILES C12OCCOCCOC3=C(C=CC(C(C)(C)C)=C3)OCCOCCOC=1C=CC(C(C)(C)C)=C2
EPA Substance Registry System Dibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecin, 2,13(or 2,14)-bis(1,1-dimethylethyl)-6,7,9,10,17,18,20,21-octahydro- (29471-17-8)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38-36/38-22
Safety Statements  26-36-36/37
RIDADR  2811
WGK Germany  3
RTECS  HP5386500
TSCA  Yes
HazardClass  6.1
PackingGroup  III
HS Code  29329990
NFPA 704
1
2 0

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 396443 4′,4′′(5′′)-Di-tert-butyldibenzo-18-crown-6 95% 29471-17-8 1G $67.4 2022-05-15 Buy
TRC D429460 4'',4''''(5'''')-Di-tert-butyldibenzo-18-crown-6 29471-17-8 250mg $40 2021-12-16 Buy
Frontier Specialty Chemicals JK356879 4',4''(5'')-Di-tert-butyldibenzo-18-crown-6,98%,mixtureofisomers 29471-17-8 1g $86 2021-12-16 Buy
American Custom Chemicals Corporation CHM0011190 4',4"(5")-DI-TERT-BUTYLDIBENZO-18-CROWN-6 95.00% 29471-17-8 250MG $568.79 2021-12-16 Buy
American Custom Chemicals Corporation CHM0011190 4',4"(5")-DI-TERT-BUTYLDIBENZO-18-CROWN-6 95.00% 29471-17-8 1G $668.23 2021-12-16 Buy
Product number Packaging Price Buy
396443 1G $67.4 Buy
D429460 250mg $40 Buy
JK356879 1g $86 Buy
CHM0011190 250MG $568.79 Buy
CHM0011190 1G $668.23 Buy

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 Chemical Properties,Uses,Production

Description

4′,4″(5″)-Di-tert-butyldibenzo-18-crown-6 is a hydrophobic crown ether compound. This crown ether is potentially useful in studies of ion transport through non-polar regions and membranes, and has been described in the design of microsensor devices for ammonia determination based upon ammonia-mediated deprotonation of a pH indicator followed by sequestering of ammonium within the 4′,4″(5″)-Di-tert-butyldibenzo-18-crown-6 sphere.

Chemical Properties

Off-white powder

Uses

4'',4''''(5'''')-Di-tert-butyldibenzo-18-crown-6 is a hydrophobic crown ether compound..

Synthesis

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 (DTBB18C6) was synthesized using 4-tert-butyl catechol (TBC) as starting material, 2,2′-diethylene glycol di(p-touenesulfonate) as cyclization reagent, Cs2CO3 as template, and tetrahydrofuran (THF) as solvent. The reaction was carried out in a sealed environment with nitrogen, and Cs2CO3 was supplemented in three steps. Moreover, it could also be synthesized by improving the electrophilic aromatic substitution of dibenzo-18-crown-6 (DB18C6) using tert-butyl alcohol (TBA) as alkylation reagent, H3PO4 (85 wt %) as catalyst and CH2Cl2 as solvent[1-2].

References

[1] Juan Fan. “Preparation of 4′,4′′(5′′)-Di-tert-butyldibenzo-18-crown-6 Based on Electrophilic Aromatic Substitution.” Chemistry Letters 41 1 (2012): 274–276.
[1] Jun Fan. “Optimization of Synthetic Strategy of 4′4″(5″)-Di-tert-butyldibenzo-18-crown-6 Using Response Surface Methodology.” Organic Process Research & Development 17 3 (2013): 368–374.

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 Preparation Products And Raw materials

Raw materials

Preparation Products

4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 Suppliers

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4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 Spectrum

4',4''(5'')-DI-TERT-BUTYLDIBENZO-18-CROWN-6 AR,AR'-DI-TERT-BUTYLDIBENZO-18-CROWN-6 14)-bis(1,1-dimethylethyl)-ro-13(or2 4',4''(5'')-di-tert-butyldibenzo-18-crown-6, mixed isomers 4',4pi(5pi)-Di-tert-butyldibenzo-18-crown-6 4,4'-Di-tert-butyldibenzo-18-crown-6 4',4''(5'')-Di-tert-butyldibenzo-18-crown-6,94% 4',4''(5'')-di-tert-butyldibenzo-18-crown-6, mixed iso 4,45-Di-tert.-butylbenzo-18-crown-6, mixture of isomers 4',4''(5'')-Di-tert-butyldibenzo-18-crown-6 95% 4',4''(5'')-Di-tert-butyldibenzo-18-crown-6, 98%, mixture of isomers Bis(tert-butylbenzo)-18-crown-6 4prime,4primeprime(5primeprime)-Di-tert-butyldibenzo-18-crown-6 Di-(tert-butylbenzo)-18-crown-6 4',4''(5'')-DI-TERT-BUTYLDIBENZO-18-CROWN-6 29471-17-8 C28H40O6 Synthetic Reagents Crown Ethers Chelation/Complexation Compounds Crown Ethers Chelation/Complexation Compounds Synthetic Reagents