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17454-53-4

CYCLOHEXANO-18-CROWN-6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17454-53-4 Structure

  • Basic information

    1. Product Name: CYCLOHEXANO-18-CROWN-6
    2. Synonyms: HEXADECAHYDROBENZO[1,4,7,10,13,16]HEXAOXACYCLOOCTADECIN;CYCLOHEXANO-18-CROWN-6;cyclohexano-18-crown-6mixtureofcisandtrans;CYCLOHEXANO-18-CROWN-6 (CIS TRANS);Cyclohexano-18-crowm-6;CYCLOHEXANO-18-CROWN-6, 95%, MIXTURE OF CIS AND TRANS
    3. CAS NO:17454-53-4
    4. Molecular Formula: C16H30O6
    5. Molecular Weight: 318.41
    6. EINECS: N/A
    7. Product Categories: Chelation/Complexation Compounds;Crown Ethers;Synthetic Reagents
    8. Mol File: 17454-53-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 417.56°C (rough estimate)
    3. Flash Point: 112.8 °C
    4. Appearance: Clear colorless/Liquid
    5. Density: 1.108 g/mL at 20 °C(lit.)
    6. Vapor Pressure: 5.26E-08mmHg at 25°C
    7. Refractive Index: 1.4785-1.4805
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CYCLOHEXANO-18-CROWN-6(CAS DataBase Reference)
    11. NIST Chemistry Reference: CYCLOHEXANO-18-CROWN-6(17454-53-4)
    12. EPA Substance Registry System: CYCLOHEXANO-18-CROWN-6(17454-53-4)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 17454-53-4(Hazardous Substances Data)

17454-53-4 Usage

Chemical Properties

Clear colourless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 17454-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,5 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17454-53:
(7*1)+(6*7)+(5*4)+(4*5)+(3*4)+(2*5)+(1*3)=114
114 % 10 = 4
So 17454-53-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H30O6/c1-2-4-16-15(3-1)21-13-11-19-9-7-17-5-6-18-8-10-20-12-14-22-16/h15-16H,1-14H2/t15-,16-/m0/s1

17454-53-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,8,11,14,17-hexaoxabicyclo[16.4.0]docosane

1.2 Other means of identification

Product number -
Other names trans-cyclohexyl-18-crown-6

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:17454-53-4 SDS

17454-53-4Downstream Products

17454-53-4Relevant articles and documents

SYNTHESIS OF CYCLOHEXANOCROWN ETHERS UNDER CONDITIONS OF PHASE-TRANSFER CATALYSIS

Kusov, S. Z.,Lubenets, E. G.,Kobrin, V. S.

, p. 1234 - 1236 (2007/10/02)

A method was described for production of individual diastereoisomers of cyclohexanocrown ethers from the cis and trans isomers of 1,2-bis(6-chloro-1,4-dioxahexyl)cyclohexane and glycols with phase transfer catalysis.

Bis-Cyclohexyl-Crown-Ethers as Allosteric Carriers

Costero, Ana M.,Rodriguez, Santiago

, p. 6265 - 6272 (2007/10/02)

Several bis-cyclohexyl-crown-ethers have been synthesized and used as carriers for alkaline cations.These compounds should all show negative allosteric cooperativity, but only 1 exhibits an odd cation transport behavior across the liquid organic membranes. Key words: Allosteric cooperativity; cation transport; crown-ethers; Na(1+)-K(1+)-ATPase; biological model.

STEREODESIGN OF CROWN ETHERS. I. SYNTHESIS AND (13)C NMR STUDY OF TRANS- CYCLOHEXANOCROWN ETHERS

Samoshin, V. V.,Zelenkina, O. A.,Subbotin, O. A.,Sergeev, N. M.,Zefirov, N. S.

, p. 413 - 418 (2007/10/02)

A series of trans-cyclohexanocrown ethers were synthesized by the intermolecular cyclization of polyethylene glycol trans-2-hydroxycyclohexyl ethers with the ditosyl derivatives of polyethylene glycols.A complete assignment of the signals in the (13)C NMR spectra was made for the obtained compounds.

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