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methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethylporphyrin-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21H,23H-Porphine-2-propanoicacid,8,13-diethyl-18-(methoxycarbonyl)-20-(2-methoxy-2-oxoethyl)-3,7,12,17-tetramethyl-,methyl ester (9CI)

    Cas No: 28211-96-3

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  • 28211-96-3 Structure
  • Basic information

    1. Product Name: methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethylporphyrin-2-carboxylate
    2. Synonyms: 21H,23H-Porphine-2-propanoic acid, 8,13-diethyl-18-(methoxycarbonyl)-20-(2-methoxy-2-oxoethyl)-3,7,12,17-tetramethyl-, methyl ester (9CI)
    3. CAS NO:28211-96-3
    4. Molecular Formula: C37H42N4O6
    5. Molecular Weight: 638.7526
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 28211-96-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1066.4°C at 760 mmHg
    3. Flash Point: 598.7°C
    4. Appearance: N/A
    5. Density: 1.219g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.586
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethylporphyrin-2-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethylporphyrin-2-carboxylate(28211-96-3)
    12. EPA Substance Registry System: methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethylporphyrin-2-carboxylate(28211-96-3)
  • 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: 28211-96-3(Hazardous Substances Data)

28211-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28211-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,1 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28211-96:
(7*2)+(6*8)+(5*2)+(4*1)+(3*1)+(2*9)+(1*6)=103
103 % 10 = 3
So 28211-96-3 is a valid CAS Registry Number.

28211-96-3SDS

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 methyl 7,12-diethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethyl-22,23-dihydroporphyrin-2-carboxylate

1.2 Other means of identification

Product number -
Other names Chloroporphyrin-e6-trimethyl 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:28211-96-3 SDS

28211-96-3Downstream Products

28211-96-3Relevant articles and documents

The Synthetic Utility and Mechanisms of the Hydrogen Iodide Isomerization and the Oxo Reaction in the Modification of Chlorophyll Derivatives

Hynninen, Paavo H.

, p. 835 - 840 (2007/10/02)

Hydrogen iodide in glacial acetic acid has served as a versatile reagent in modifications of chlorophyll and its closely related derivatives, e. g. pheophorbides and 3-vinylchlorins, to 3-ethylporphyrins (HI isomerization) or to 31-oxoporphyrins (oxo reaction).Nevertheless, the mechanisms of these important reactions have remained obscure.In this paper, the reaction conditions used by H.Fischer for the HI isomerization and the oxo reaction are thoroughly examined.Secondly, a carbocation rearrangement mechanism is suggested for the the HI isomerization.Thirdly, the oxo reaction is rationalized by means of a reaction between a chlorin 31-carbocation and water nucleophile and subsequent dehydrogenation by triplet oxygen.Finally, some related unsolved problems of chlorophyll chemistry are briefly discussed.

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