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53454-78-7

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53454-78-7 Usage

Appearance

Yellow crystalline solid

Solubility

Insoluble in water

Melting point

High melting point (exact value not provided)

Organic chemistry

Used in the synthesis of other organic compounds

Reagent

Utilized in chemical reactions

Building block

Employed in the production of pharmaceuticals and specialty chemicals

Commercial availability

Limited, not commonly used in large-scale industrial processes

Research status

Exact uses and properties are still being researched and explored in the scientific community

Check Digit Verification of cas no

The CAS Registry Mumber 53454-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,5 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53454-78:
(7*5)+(6*3)+(5*4)+(4*5)+(3*4)+(2*7)+(1*8)=127
127 % 10 = 7
So 53454-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O4/c19-15(13-7-3-1-4-8-13)11-17(21)18(22)12-16(20)14-9-5-2-6-10-14/h1-10H,11-12H2

53454-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-diphenylhexane-1,3,4,6-tetrone

1.2 Other means of identification

Product number -
Other names 1,6-Diphenyl-hexan-1,3,4,6-tetraon

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:53454-78-7 SDS

53454-78-7Relevant articles and documents

Metal-directed formation of tetra-, hexa-, octa-, and nonanuclear complexes of magnesium, calcium, manganese, copper, and cadmium

Saalfrank, Rolf W.,Lo?w, Norbert,Demleitner, Bernhard,Stalke, Dietmar,Teichert, Markus

, p. 1305 - 1311 (2007/10/03)

Reactions of bis-1,3-dicarbonyl compounds H2L (1) with metal dichlorides of cadmium, manganese and calcium in the presence of aqueous ammonia affords octanuclear supramolecular coordination complexes [M8L8]·4Y (2-5), whereas reaction with magnesium dichloride yields an adamantanoid tetranuclear cluster [(4NH4) · (Mg4L6/a)] (6). Treatment of copper dichloride with diethyl ketipinate 1a and sodium hydroxide furnishes the double-/triple-decker metallacoronares [{[Na · (Cu3L3/a)BF4]·THF·H2O}2] (7) and [{Nac · (Cu3L3a)BF4}3·2THF] (8) with an encapsulated sodium ion. Since the 1H and 13C NMR spectra of diamagnetic 2 and 5 and paramagnetic 4, 7 and 8 do not unambiguously establish the exact Structure of these compounds, exemplary X-ray diffraction analyses of 4, 7 and 8 were carried out.

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