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3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 123279-53-8 Structure
  • Basic information

    1. Product Name: 3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester
    2. Synonyms: 3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester
    3. CAS NO:123279-53-8
    4. Molecular Formula: C36H34F4N4O4
    5. Molecular Weight: 662.6731728
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 123279-53-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1011.5°Cat760mmHg
    3. Flash Point: 565.5°C
    4. Appearance: /
    5. Density: 1.293g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.591
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester(123279-53-8)
    12. EPA Substance Registry System: 3(2),3(2),8(2),8(2)-tetrafluoroprotoporphyrin dimethyl ester(123279-53-8)
  • 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: 123279-53-8(Hazardous Substances Data)

123279-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123279-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,7 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123279-53:
(8*1)+(7*2)+(6*3)+(5*2)+(4*7)+(3*9)+(2*5)+(1*3)=118
118 % 10 = 8
So 123279-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C36H34F4N4O4/c1-17-21(7-9-35(45)47-5)29-16-30-22(8-10-36(46)48-6)18(2)27(42-30)14-31-24(12-34(39)40)20(4)28(44-31)15-32-23(11-33(37)38)19(3)26(43-32)13-25(17)41-29/h11-16,43-44H,7-10H2,1-6H3/b25-13-,26-13-,27-14-,28-15-,29-16-,30-16-,31-14-,32-15-

123279-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[8,13-bis(2,2-difluoroethenyl)-18-(3-methoxy-3-oxopropyl)-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoate

1.2 Other means of identification

Product number -
Other names 21H,23H-Porphine-2,18-dipropanoic acid,7,12-bis(2,2-difluoroethenyl)-3,8,13,17-tetramethyl-,dimethyl ester

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:123279-53-8 SDS

123279-53-8Downstream Products

123279-53-8Relevant articles and documents

High sensitivity of the fluorine NMR signals of difluorovinyl analogs of natural hemin: Reconstituted heme proteins and self-exchange electron transfer in model compounds

Poliart, Christine,Briand, Jean-Francois,Tortevoie, Frederique,Leroy, Jacques,Simonneaux, Gerard,Bondon, Arnaud

, p. 615 - 620 (2001)

The chemical shifts of fluorine in difluorovinyl deuteroporphyrin iron complexes were shown to be very sensitive to the spin state of the metal and the nature of the ligand(s). Reconstituted myoglobin was used as a model heme protein with an exchangeable heme. Large variations in the fluorine chemical shifts in both the ferric and ferrous states were observed. This strong sensitivity to the nature of the metal ligand and the structural resemblance to natural hemin make this fluorinated porphyrin a good probe for the study of heme proteins. The large variations of chemical shifts depending on the oxidation state also permitted the measurement of the electron self-exchange rate constants of bis(1-methylimidazole)iron complexes in various solvents by analysis of line broadening of the 19F NMR signals. The experimental rate constants were strongly affected by the nature of the solvent, varying from 3.9 × 107 to 24.1 × 108 mol I-1 s-1 for DMSO-d6 and acetone-d6, respectively. The solvent parameters were used to estimate the outer-sphere reorganization energies. The experimental rate constants in chloroform and in DMSO are in good agreement with these calculated outer-sphere reorganization energies. Copyright

Synthesis of Fluorine Analogues of Protoporphyrin

Ando, Akira,Shinada, Tetsuro,Kinoshita, Shinji,Arimura, Noriko,Nagai, Takabumi,et al.

, p. 293 - 298 (1989)

With intention of obtaining a porphyrin derivative useful for diagnosis and therapy of cancer, fluorine analogues of protoporphyrin, in which the vinyl group(s) are replaced by difluorovinyl group(s), were synthesized by the reaction of the formylporphyrins with sodium chlorodifluoroacetate in the presence of triphenylphosphine.

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