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240797-81-3

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240797-81-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in the compound, which in this case is 17 carbon (C), 28 hydrogen (H), 2 nitrogen (N), 2 oxygen (O), and 2 sulfur (S) atoms.
2. Heterocyclic compound

Explanation

A heterocyclic compound is a cyclic compound containing atoms of at least two different elements, in this case, carbon, oxygen, sulfur, and nitrogen.

Explanation

The compound contains two oxygen atoms, which are part of the dioxa (O2) group in the structure.

Explanation

The compound contains two sulfur atoms, which are part of the dithia (S2) group in the structure.

Explanation

The compound contains one nitrogen atom, which is part of the aza (N) group in the structure.
6. Presence of a phenyl group

Explanation

The compound contains a phenyl group, which is a six-carbon aromatic ring with alternating single and double bonds.
7. Industrial applications

Explanation

1,4-Dioxa-7,13-dithia-10-azacyclopentadecane, 10-phenylis used in various industrial applications, such as the synthesis of pharmaceuticals, agrochemicals, and materials science.
8. Versatile compound

Explanation

Due to its unique structure and combination of elements, the compound is considered versatile and important in the field of organic chemistry.
9. Chemical processes

Explanation

The compound is involved in various chemical processes, making it a valuable component in the synthesis of different products.

Presence of oxygen atoms

2

Presence of sulfur atoms

2

Presence of nitrogen atoms

1

Check Digit Verification of cas no

The CAS Registry Mumber 240797-81-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,7,9 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 240797-81:
(8*2)+(7*4)+(6*0)+(5*7)+(4*9)+(3*7)+(2*8)+(1*1)=153
153 % 10 = 3
So 240797-81-3 is a valid CAS Registry Number.

240797-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-phenyl-1,4-dioxa-7,13-dithia-10-azacyclopentadecane

1.2 Other means of identification

Product number -
Other names 10-phenyl-10-aza-1,4-dioxa-7,13-dithiacyclopentadecane

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:240797-81-3 SDS

240797-81-3Relevant articles and documents

Cation exchange reversibly switches rotor speed and is monitored by a networked fluorescent reporter

?zer, Merve S.,Paul, Indrajit,Goswami, Abir,Schmittel, Michael

, p. 9043 - 9047 (2019)

Framework 1, a freely rotating turnstile, is transformed by sequential metal ion addition into the coordination-based double-minimum rotors [M2(1)]2n+ that operate at 8 kHz (M = Zn2+; n = 2) and 30 kHz (M = Cu+; n = 1). In a network with the fluorescent receptor 2, the metal ion exchange at [M2(1)]2n+ and thus indirectly the rotor speed is reported by distinct fluorescence changes at 2.

Multi-channel receptors and their relation to guest chemosensing and reconfigurable molecular logic gates

Jimenez, Diego,Martinez-Manez, Ramon,Sancenon, Felix,Ros-Lis, Jose V.,Soto, Juan,Benito, Angel,Garcia-Breijo, Eduardo

, p. 2393 - 2403 (2005)

The synthesis and characterisation of a family of multi-channel receptors containing crown-cation binding sites anchored to a 1-aminophenyl-1,2,2- tricyanoethylene group is reported. The ligands L1-L6bear a 1-aminophenyl-1,2,2-tricyanoethylene scaffolding which is simultaneously a redox-active group (showing reduction processes at moderately modest potentials) and an acceptor moiety in the 1-aminophenyl-1,2,2-tricyanoethylene chromophore. Additionally, dyes L1-L6 also show fluorescence emission. The colour variation of L1-L6 in acetonitrile in the presence of the metal cations Ag+, Cd2+, Cu2+, Fe2+, Hg2+, Pb2+ and Zn2+ has been studied. Selective hypsochromic shifts were found for the systems L 4-Pb2+, L5-Hg2+ and L 6-Hg2+ For Hg2+ with L5 and L 6 and Pb2+ with L4, emission fluorescence enhancements most likely associated with metal coordination to the anilinium nitrogen were observed. The electrochemical behaviour of receptors L 1-L6 was studied in acetonitrile with platinum as working electrode and [Bu4N][BF4] as supporting electrolyte. This family of receptors shows a one-electron reversible reduction process at around -0.70 V vs. SCE, attributed to the reduction of the tricyanovinyl group. Additionally, all the receptors also show the oxidation of the anilinium moiety at about 1.2-1.4 V vs. SCE. Significant anodic shifts of both reduction and oxidation waves were found in the presence of certain metal cations. The relationship of these multiple-channel signalling receptors with guest chemosensing and reconfigurable molecular-based logic gates is discussed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.

Solvent effect and amine interference on colorimetric changes of azobenzene-conjugated dithiaazadioxo crown ether mercury sensor

Jeon, Chang Hoon,Lee, Jayeon,Ahn, Sang Jung,Ha, Tai Hwan

, p. 6841 - 6847 (2019/04/10)

The colorimetric behavior of an azobenzene-based dye containing dithiaazadioxo ring for Hg2+-detection was investigated in diverse solvents. The mercury specific ligand shows hypsochromic changes in pure and aqueous MeCN upon Hg2+-bi

A near IR di-styryl BODIPY-based ratiometric fluorescent chemosensor for Hg(II)

Atilgan, Serdar,Kutuk, Ilker,Ozdemir, Tugba

supporting information; experimental part, p. 892 - 894 (2010/05/03)

A novel BODIPY-based near-IR emitting probe as a selective and sensitive fluorophore for Hg(II) is synthesized. This versatile BODIPY fluorophore is functionalized for long wavelength emission at the 3 and 5 positions via a condensation reaction in which

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