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69912-09-0

3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 69912-09-0 Structure

  • Basic information

    1. Product Name: 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester
    2. Synonyms: 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester
    3. CAS NO:69912-09-0
    4. Molecular Formula:
    5. Molecular Weight: 273.288
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 69912-09-0.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: 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester(69912-09-0)
    11. EPA Substance Registry System: 3,5-dimethylpyrrole-2,4-dicarboxylic acid 2-benzyl ester(69912-09-0)

  • 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: 69912-09-0(Hazardous Substances Data)

69912-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69912-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,1 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 69912-09:
(7*6)+(6*9)+(5*9)+(4*1)+(3*2)+(2*0)+(1*9)=160
160 % 10 = 0
So 69912-09-0 is a valid CAS Registry Number.

69912-09-0Relevant articles and documents

Synthesis and pharmacological characterisation of 2,4-dicarboxy-pyrroles as selective non-competitive mGluR1 antagonists.

Micheli, Fabrizio,Fabio, Romano Di,Cavanni, Paolo,Rimland, Joseph M,Capelli, Anna Maria,Chiamulera, Cristiano,Corsi, Mauro,Corti, Corrado,Donati, Daniele,Feriani, Aldo,Ferraguti, Francesco,Maffeis, Micaela,Missio, Andrea,Ratti, Emiliangelo,Paio, Alfredo,Pachera, Roberta,Quartaroli, Mauro,Reggiani, Angelo,Sabbatini, Fabio Maria,Trist, David G,Ugolini, Annarosa,Vitulli, Giovanni

, p. 171 - 183 (2003)

Metabotropic glutamate receptors (mGluRs) are an unusual family of G-protein coupled receptor (GPCR), and are characterised by a large extracellular N-terminal domain that contains the glutamate binding site. We have identified a new class of non-competit

Asymmetric synthesis of mono- and dinuclear bis(dipyrrinato) complexes

Ali, Adeeb Al-Sheikh,Benson, Ronald E.,Blumentritt, Sascha,Cameron, T. Stanley,Linden, Anthony,Wolstenholme, David,Thompson, Alison

, p. 4947 - 4952 (2008/02/05)

(Chemical Equation Presented) The diastereoselective syntheses of Zn(II) bis(dipyrrinato) helicates is reported, involving ligands templated by the incorporation of homochiral binol within the linker joining the two dipyrrinato units. The most diastereose

Efficient method for the synthesis of bisaminoethanethiols and their pyrrole conjugates

Li, Guolin,Ma, Qinggago,Ma, Bing,Grossman, Zachary D.,Pandey, Ravindra K.

, p. 2849 - 2854 (2007/10/03)

By following the protection and deprotection approach, an efficient method for the preparation of bisaminoethanethiol ligands (N2S2) is discussed. In our attempts to synthesize certain nonpeptide analogs of neurotensin, moldel studies were performed by using these ligands for preparing the corresponding pyrrole based conjugates. This methodology provides an alternate approach for developing various target specific agents that cross the blood brain barrier.

TOTAL SYNTHESES OF MONO-, DI-, AND TRI-PROPIONIC PORPHYRINS FOR STUDIES OF THE MECHANISM OF HEME-APOPROTEIN RECONSTITUTION

Pandey, Ravindra K.,Rezzano, Irene N.,Smith, Kevin M.

, p. 2171 - 2192 (2007/10/02)

Total syntheses of eight new porphyrins bearing either one (14), two (8, 15, 28, 29, 51) or three (42, 43) propionic side chains in variously permutated positions around the porphyrin periphery are described.Compound (8) was prepared using the MacDonald (

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