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103542-42-3

Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester is a complex organic compound with the chemical formula C26H21NO3. It is a derivative of benzenepentanoic acid, featuring a 7-phenyl-1,10-phenanthrolin-4-yl group attached to the 4-position of the benzene ring. The molecule is further characterized by a methyl ester functional group, which is formed by the esterification of the carboxylic acid group with methanol. Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester is known for its potential applications in the field of chemistry, particularly in the synthesis of various pharmaceuticals and dyes. Its structure and properties make it a valuable intermediate in organic synthesis, highlighting its importance in the development of new chemical entities.

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  • 103542-42-3 Structure

  • Basic information

    1. Product Name: Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester
    2. Synonyms:
    3. CAS NO:103542-42-3
    4. Molecular Formula: C30H26N2O2
    5. Molecular Weight: 446.549
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103542-42-3.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: Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester(103542-42-3)
    11. EPA Substance Registry System: Benzenepentanoic acid, 4-(7-phenyl-1,10-phenanthrolin-4-yl)-, methyl ester(103542-42-3)

  • 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: 103542-42-3(Hazardous Substances Data)

103542-42-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103542-42-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,4 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 103542-42:
(8*1)+(7*0)+(6*3)+(5*5)+(4*4)+(3*2)+(2*4)+(1*2)=83
83 % 10 = 3
So 103542-42-3 is a valid CAS Registry Number.

103542-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-[4-(7-phenyl-1,10-phenanthrolin-4-yl)phenyl]pentanoate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:103542-42-3 SDS

103542-42-3Relevant articles and documents

A new robust and highly sensitive FRET donor-acceptor pair: Synthesis, characterization, and application in a thrombin assay

Kainmueller, Eva K.,Bannwarth, Willi

, p. 3056 - 3070 (2008/01/27)

The synthesis of a new, robust fluorescence-resonance-energy-transfer (FRET) system is described. Its donor chromophore is derived from an N-allyl-substituted quinolinone attached to 4-bromophenyl-alanine via Heck cross-coupling. The resulting Fmoc-protected derivative 11 was used as building block in solid-phase peptide synthesis (SPPS). As FRET acceptor, a sulfonylated ruthenium(II)-bathophenanthroline complex with a peripheral COOH function was prepared for covalent attachment to target molecules. The UV/VIS absorption and emission spectra of peptides bearing only the donor (D) or acceptor (A) dye showed a good overlap of the emission band of the donor with the absorption band of the acceptor. The fluorescence spectra of a peptide bearing both dyes revealed an additional emission after excitation of the donor, which is due to indirect excitation of the acceptor via FRET. The long fluorescence lifetime of the RuII complex (0.53 μs) makes it well-suited for time-resolved measurements. As a first application of this new FRET system, the peptide 18, with the recognition sequence for the protease thrombin, flanked by the two dyes, was synthesized and successfully cleaved by the enzyme. The change in the ratio of the fluorescence intensities could be determined.

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