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137131-35-2

5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic 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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  • 137131-35-2 Structure

  • Basic information

    1. Product Name: 5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester
    2. Synonyms: 5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester
    3. CAS NO:137131-35-2
    4. Molecular Formula:
    5. Molecular Weight: 157.169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 137131-35-2.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: 5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester(137131-35-2)
    11. EPA Substance Registry System: 5-methoxy-3,4-dihydro-2H-pyrrole-2-carboxylic acid methyl ester(137131-35-2)

  • 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: 137131-35-2(Hazardous Substances Data)

137131-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137131-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,1,3 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 137131-35:
(8*1)+(7*3)+(6*7)+(5*1)+(4*3)+(3*1)+(2*3)+(1*5)=102
102 % 10 = 2
So 137131-35-2 is a valid CAS Registry Number.

137131-35-2Relevant articles and documents

Impact of Functional Groups on the Copper-Initiated N-Arylation of 5-Functionalized Pyrrolidin-2-ones and Their Vinylogues

Baudelet, Davy,Da?ch, Adam,Rigo, Beno?t,Lipka, Emmanuelle,Gautret, Philippe,Homerin, Germain,Claverie, Christelle,Rousseau, Jolanta,Abuhaie, Cristina-Maria,Ghinet, Alina

supporting information, p. 2226 - 2244 (2016/07/15)

The electronic effects governing the N-arylation of pyrrolidone were investigated. The generalization of our preliminary findings on a copper(I)-catalyzed Csp2-N coupling process was first improved with a wide variety of aryl and heteroaryl halides and methyl pyroglutamate. The optimized protocol was further extended to pyrrolidin-2-ones substituted at the C5-position with an aryl group bearing an electron-donating or electron-withdrawing group as well as to some of their substituted enaminoester vinylogues. The impact of substituents at the N- and C5-position on these coupling processes seemed to be pivotal for determining both the reaction profiles and yields.

HYDROXYMETHYL PYRROLIDINES AS BETA 3 ADRENERGIC RECEPTOR AGONISTS

-

Page/Page column 46, (2009/10/30)

The present invention provides compounds of Formula I, pharmaceutical compositions thereof, and method of using the same in the treatment or prevention of diseases mediated by the activation of β3-adrenoceptor.

SYNTHESIS OF 3,5-TRANS-3-METHOXYCARBONYL-1-CARBAPENAM FROM METHYL (+/-)-PYROGLUTAMATE

Nagasaka, Tatsuo,Tsukada, Atsuhiko,Hamaguchi, Fumiko

, p. 2015 - 2022 (2007/10/02)

Synthesis of 3,5-trans-3-methoxycarbonyl-1-carbapenam in six steps from methyl (+/-)-pyroglutamate is described.

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