7397-92-4 Usage
Description
1-Bromoanthracene, with the molecular formula C14H9Br, is an organic chemical compound derived from anthracene, a polycyclic aromatic hydrocarbon. It is commonly utilized as a starting material in organic synthesis and serves as a building block for the production of various aromatic compounds.
Uses
Used in Organic Synthesis:
1-Bromoanthracene is used as a starting material for the synthesis of other organic compounds, providing a foundation for the creation of a wide range of chemical products.
Used in Aromatic Compound Production:
1-Bromoanthracene is used as a building block in the production of various aromatic compounds, contributing to the development of complex organic molecules.
Used in Dye and Pigment Manufacturing:
1-Bromoanthracene is employed in the manufacturing of dyes and pigments, playing a role in the coloration of various products.
Used in Pharmaceutical Production:
1-Bromoanthracene is used in the production of pharmaceuticals, potentially contributing to the development of new drugs and medications.
Safety Precautions:
Due to its potential health and environmental hazards, it is crucial to follow proper safety precautions and protective measures when handling 1-Bromoanthracene.
Check Digit Verification of cas no
The CAS Registry Mumber 7397-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7397-92:
(6*7)+(5*3)+(4*9)+(3*7)+(2*9)+(1*2)=134
134 % 10 = 4
So 7397-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Br/c15-14-7-3-6-12-8-10-4-1-2-5-11(10)9-13(12)14/h1-9H
7397-92-4Relevant articles and documents
BIARYL HYDROXYTHIOPHENE GROUP IV TRANSITION METAL POLYMERIZATION CATALYSTS WITH CHAIN TRANSFER CAPABILITY
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, (2022/02/05)
Catalyst systems that include a chain transfer agent and a metal-ligand complex according to formula (I).
Syntheses and Absolute Stereochemistry of Chiral 9,10-Dihydro-9,10-ethanoanthracenes and their Tricarbonylchromium Complexes
Li, Z.,Werner, A.,Schloegl, K.
, p. 441 - 452 (2007/10/02)
Several chiral mono- and disubstituted 9,10-dihydro-9,10-ethanoanthracenes have been prepared from the corresponding anthracenes.Most of them were separated into enantiomers by chromatography on cellulose triacetate (CTA) and their absolute chiralities established by chiroptical comparison (via their CD spectra) with key compounds of known configuration.From the laevorotatory 1,5-dibromo derivative 16 the dextrorotatory dideuterio hydrocarbon (+)(9S,10S)-20 was obtained.Complexation of 2,6-dimethyl 9,10-dihydro-9,10-ethanoanthracene (+)-25, obtained by enantioselective chromatography on CTA , with Cr(CO)6 afforded two mono tricarbonylchromium complexes as well as the bis-exo,endo-complex (+)-28.Configurational assignments (exo,endo) are based on the absorption patterns of the bridge protons in the 1H NMR spectra. Keywords: (+)-1,5-Dideuterio-9,10-dihydro-9,10-ethanoanthracene; Enantioselective chromatography on CTA; Circular dichroism; Configurational correlation; Tricarbonylchromium complexes.
Anthracene 1,2-oxide: synthesis and role in the metabolism of anthracene by mammals.
Akhtar,Hamilton,Boyd,Braunstein,Seifried,Jarina
, p. 1442 - 1446 (2007/10/11)
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