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Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)-

    Cas No: 216852-10-7

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  • 216852-10-7 Structure
  • Basic information

    1. Product Name: Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)-
    2. Synonyms:
    3. CAS NO:216852-10-7
    4. Molecular Formula: C18H27NO6
    5. Molecular Weight: 353.415
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 216852-10-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)-(216852-10-7)
    11. EPA Substance Registry System: Benzaldehyde, 3-methoxy-4-(1,4,7,10-tetraoxa-13-azacyclopentadec-13-yl)-(216852-10-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 216852-10-7(Hazardous Substances Data)

216852-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216852-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,8,5 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 216852-10:
(8*2)+(7*1)+(6*6)+(5*8)+(4*5)+(3*2)+(2*1)+(1*0)=127
127 % 10 = 7
So 216852-10-7 is a valid CAS Registry Number.

216852-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-formyl-2-methoxyphenylaza-15-crown-5

1.2 Other means of identification

Product number -
Other names 3-Methoxy-4-(1,4,7,10-tetraoxa-13-aza-cyclopentadec-13-yl)-benzaldehyde

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:216852-10-7 SDS

216852-10-7Relevant articles and documents

A fluorescent combinatorial logic gate with Na+, H+-enabled or and H+-driven low-medium-high ternary logic functions

Spiteri, Jasmine M. A.,Mallia, Carl J.,Scerri, Glenn J.,Magri, David C.

, p. 10116 - 10121 (2017)

A novel fluorescent molecular logic gate with a 'fluorophore-spacer1-receptor1-spacer2-receptor2' format is demonstrated in 1:1 (v/v) methanol/water. The molecule consists of an anthracene fluorophore, and terti

Na+ Selective Fluorescent Tools Based on Fluorescence Intensity Enhancements, Lifetime Changes, and on a Ratiometric Response

Schwarze, Thomas,Riemer, Janine,Müller, Holger,John, Leonard,Holdt, Hans-Jürgen,Wessig, Pablo

, p. 12412 - 12422 (2019/09/06)

Over the years, we developed highly selective fluorescent probes for K+ in water, which show K+-induced fluorescence intensity enhancements, lifetime changes, or a ratiometric behavior at two emission wavelengths (cf. Scheme 1, K1–K4). In this paper, we introduce selective fluorescent probes for Na+ in water, which also show Na+ induced signal changes, which are analyzed by diverse fluorescence techniques. Initially, we synthesized the fluorescent probes 2, 4, 5, 6 and 10 for a fluorescence analysis by intensity enhancements at one wavelength by varying the Na+ responsive ionophore unit and the fluorophore moiety to adjust different Kd values for an intra- or extracellular Na+ analysis. Thus, we found that 2, 4 and 5 are Na+ selective fluorescent tools, which are able to measure physiologically important Na+ levels at wavelengths higher than 500 nm. Secondly, we developed the fluorescent probes 7 and 8 to analyze precise Na+ levels by fluorescence lifetime changes. Herein, only 8 (Kd=106 mm) is a capable fluorescent tool to measure Na+ levels in blood samples by lifetime changes. Finally, the fluorescent probe 9 was designed to show a Na+ induced ratiometric fluorescence behavior at two emission wavelengths. As desired, 9 (Kd=78 mm) showed a ratiometric fluorescence response towards Na+ ions and is a suitable tool to measure physiologically relevant Na+ levels by the intensity change of two emission wavelengths at 404 nm and 492 nm.

Preparation method of Na molecular fluorescent intermediate and preparation method of Na molecular fluorescent sensor

-

Paragraph 0098; 0112-0114; 0166-0167, (2019/01/04)

The invention provides a preparation method of a Na molecular fluorescent intermediate and a preparation method of a Na molecular fluorescent sensor. The Na molecular fluorescent intermediatehas a structure as shown in a formula I. The preparation method of the Na molecular fluorescent intermediate comprises the following steps: S1, carrying out a substitution reaction on o-anisidineand alpha-methyl haloacetate to obtain a compound 2; S2, carrying out a reduction reaction on the compound 2 to obtain a compound 3; S3, carrying out a hydroxyl substitution on the compound 4 by adopting toluene sulfonyl chloride to obtain a compound 5, wherein the compound 4 has a structural formula as the follows; S4, carrying out a cyclization reaction on the compound 3 and the compound 5 to obtain a compound 6; S5, carrying out a formylation reaction on the compound 6 to obtain a compound 7; S6, carrying out a henry reaction on the compound 7 with nitromethane to obtain a compound 8; and S7, carrying out nitroso reduction reaction on the compound 8 to obtain the Na molecular fluorescent intermediate. The method is beneficial to improving the yield of the Na molecular fluorescentintermediate.

Sodium-Selective Fluoroionophore-Based Optodes for Seawater Salinity Measurement

Müller, Bernhard J.,Rappitsch, Tanja,Staudinger, Christoph,Rüschitz, Christian,Borisov, Sergey M.,Klimant, Ingo

, p. 7195 - 7202 (2017/07/22)

A new fluorescent sensor for Na+ is presented. The sensor relies on a Na+ selective fluoroionophore based on a bright red-emitting BODIPY chromophore. The fluorescence of the fluoroionophore is enhanced upon binding of Na+-ions to the highly selective aza-crown ether receptor due to reduction of the photoinduced electron transfer (PET) quenching. Solid state sensing materials were prepared by physically embedding the fluoroionophore into water-swellable biocompatible polymer matrices (polyurethane hydrogels), thus enabling continuous measurements of aqueous samples. Despite the simple design, the sensor showed no leaching of the indicator and featured fast and reversible response. Among different polyurethane hydrogels investigated, the hydrogel D1 featuring the highest water uptake was found to be the most suitable due to the highest dynamics between "off" and "on" states. Due to little or no cross sensitivity to other ions (e.g., Mg2+, Ca2+, K+) and its insensitivity to potential changes in pH, this sensor is promising for use in clinical diagnostics and for biological and marine applications. Fiber-optic sensors based on referenced read-out with a compact phase fluorimeter were prepared. To demonstrate their practical applicability, the sensors were used to determine the salinity in the seawater and brackish water of the Baltic Sea.

A fluorescent chemosensor for sodium based on photoinduced electron transfer

He, Huarui,Mortellaro, Mark A.,Leiner, Marc J. P.,Young, Susanne T.,Fraatz, Robert J.,Tusa, James K.

, p. 549 - 555 (2007/10/03)

A new optical sensor suitable for practical measurement of sodium in serum and whole blood samples is described. The optical sensor is based on a novel PET (photoinduced eletron transfer) fluoroionophore immobilized in a hydrophilic polymer layer. The des

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