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CAS

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1191423-01-4

4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1191423-01-4 Structure

  • Basic information

    1. Product Name: 4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde
    2. Synonyms: 4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde
    3. CAS NO:1191423-01-4
    4. Molecular Formula:
    5. Molecular Weight: 343.541
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191423-01-4.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: 4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde(1191423-01-4)
    11. EPA Substance Registry System: 4-(3-phenylpropyl)-1-(2-(trimethylsilyl)ethoxymethyl)-1H-pyrrole-2-carbaldehyde(1191423-01-4)

  • 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: 1191423-01-4(Hazardous Substances Data)

1191423-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191423-01-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,4,2 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1191423-01:
(9*1)+(8*1)+(7*9)+(6*1)+(5*4)+(4*2)+(3*3)+(2*0)+(1*1)=124
124 % 10 = 4
So 1191423-01-4 is a valid CAS Registry Number.

1191423-01-4Relevant articles and documents

Synthesis and matrix metalloproteinase-12 inhibitory activity of ageladine A analogs

Ando, Naoki,Terashima, Shiro

, p. 579 - 596 (2011)

Synthesis of the 37 ageladine A analogs was accomplished by employing the total synthetic route of natural ageladine A previously explored by us. From the matrix metalloproteinase-12 (MMP-12) inhibitory activity assay carried out using the novel analogs, it appeared evident that the halogen atom at the 2-position of pyrrole ring was essential for the inhibitory activity and that the introduction of a bromine atom into the 4-position of pyrrole ring is very effective for producing potent activity. In addition, exchange of the pyrrole ring to an imidazole ring was extremely effective in increasing activity, and the analog 29 thus obtained was found to show approximately 4 times more potent activity than natural ageladine A.

Synthesis of novel ageladine A analogs showing more potent matrix metalloproteinase (MMP)-12 inhibitory activity than the natural product

Ando, Naoki,Terashima, Shiro

scheme or table, p. 5461 - 5463 (2010/05/02)

By employing a previously established synthetic scheme, the synthesis described in the title was carried out in order to explore the substituent effects in the pyrrole ring of ageladine A on MMP-12 inhibitory activity. It became evident that a halogen ato

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