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CAS

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103423-07-0

2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 103423-07-0 Structure

  • Basic information

    1. Product Name: 2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester
    2. Synonyms: 2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester
    3. CAS NO:103423-07-0
    4. Molecular Formula:
    5. Molecular Weight: 281.419
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 103423-07-0.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: 2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester(103423-07-0)
    11. EPA Substance Registry System: 2-[2-(2,4,6-Trimethyl-phenylsulfanyl)-ethylamino]-propionic acid methyl ester(103423-07-0)

  • 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: 103423-07-0(Hazardous Substances Data)

103423-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103423-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,2 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 103423-07:
(8*1)+(7*0)+(6*3)+(5*4)+(4*2)+(3*3)+(2*0)+(1*7)=70
70 % 10 = 0
So 103423-07-0 is a valid CAS Registry Number.

103423-07-0Downstream Products

103423-07-0Relevant articles and documents

Inactivation of Cytochrome P-450 during Catalytic Oxidation of a 3-sydnone: N-Vinyl Heme Formation via Insertion into the Fe-N Bond

Montellano de, Paul R. Ortiz,Grab, Lawrence A.

, p. 5584 - 5589 (1986)

A 3--4-methylsydnone has been synthesized and shown to destroy hepatic microsomal cytochrome P-450 in a time- and NADPH-dependent manner.Enzyme destruction is accompanied by the formation of pyruvic acid and a green hepatic pigment.The pigment has been purified and identified by analytical and spectroscopic methods as a mixture of the four isomers of N-vinylprotoporphyrin IX.The results indicate that enzyme-catalyzed hydroxylation of the sydnone anionic carbon fragments the heterocyclic ring into pyruvic acid and a 2-(arylthio)ethyl diazonium species that reacts with the prosthetic heme group.Internal elimination of the arylthio moiety from a bridged Fe-CHR-N adduct rationalizes the formation of N-vinylprotoporphyrin IX.The results provide strong support for the biological formation of bridged Fe-C-N species and an explanation for some of the biological activities of the sydnones.

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