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CAS

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293732-35-1

1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 293732-35-1 Structure

  • Basic information

    1. Product Name: 1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodophenyl)methyl]-
    2. Synonyms:
    3. CAS NO:293732-35-1
    4. Molecular Formula: C16H19IN2O
    5. Molecular Weight: 382.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 293732-35-1.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: 1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodophenyl)methyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodophenyl)methyl]-(293732-35-1)
    11. EPA Substance Registry System: 1H-Pyrrole-2-carboxamide, N,N-diethyl-1-[(2-iodophenyl)methyl]-(293732-35-1)

  • 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: 293732-35-1(Hazardous Substances Data)

293732-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 293732-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,7,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 293732-35:
(8*2)+(7*9)+(6*3)+(5*7)+(4*3)+(3*2)+(2*3)+(1*5)=161
161 % 10 = 1
So 293732-35-1 is a valid CAS Registry Number.

293732-35-1Relevant articles and documents

Metalation-cyclisation sequence on N-(o-halobenzyl)pyrroles. Synthesis of pyrrolo[1,2-b]isoquinolones

Ardeo, Ainhoa,Lete, Esther,Sotomayor, Nuria

, p. 5211 - 5214 (2000)

Parham-type cyclisation of N-(o-halobenzyl)pyrroles has been investigated. Aryllithiums generated from metalation of N-(o- iodobenzyl)pyrroles undergo intramolecular cyclisation to give pyrrolo[1,2- b]isoquinolinones in moderate to good yields, if the N,N

An efficient entry to pyrrolo[1,2-b]isoquinolines and related systems through Parham cyclisation

Ruiz, Javier,Ardeo, Ainhoa,Ignacio, Roberto,Sotomayor, Nuria,Lete, Esther

, p. 3311 - 3324 (2007/10/03)

Aryllithiums generated by lithium-iodine exchange undergo intramolecular cyclisation to give pyrrolo[1,2-b]isoquinolines, in high yields. The best results were obtained when Weinreb or morpholine amides were used as internal electrophiles. The procedure h

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