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1,2-Bi-1H-pyrrole,1-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 453590-50-6 Structure
  • Basic information

    1. Product Name: 1,2-Bi-1H-pyrrole,1-methyl-(9CI)
    2. Synonyms: 1,2-Bi-1H-pyrrole,1-methyl-(9CI)
    3. CAS NO:453590-50-6
    4. Molecular Formula: C9H10N2
    5. Molecular Weight: 146.1891
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 453590-50-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-Bi-1H-pyrrole,1-methyl-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Bi-1H-pyrrole,1-methyl-(9CI)(453590-50-6)
    11. EPA Substance Registry System: 1,2-Bi-1H-pyrrole,1-methyl-(9CI)(453590-50-6)
  • 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: 453590-50-6(Hazardous Substances Data)

453590-50-6 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, 1,2-Bi-1H-pyrrole,1-methyl-(9CI) has 9 carbon (C) atoms, 9 hydrogen (H) atoms, and 1 nitrogen (N) atom.

Explanation

1,2-Bi-1H-pyrrole,1-methyl-(9CI) is a derivative of pyrrole, which is a five-membered aromatic ring containing one nitrogen atom.

Explanation

This is another name used to refer to the same chemical compound, emphasizing its structural relationship to pyrrole.

Explanation

1,2-Bi-1H-pyrrole,1-methyl-(9CI) is structurally related to the naturally occurring pigment bilirubin, which is a product of the breakdown of hemoglobin in the body.

Explanation

The compound has potential applications in the fields of organic synthesis and materials science due to its unique structure and properties.

Explanation

As a chemical compound with unique properties, 1,2-Bi-1H-pyrrole,1-methyl-(9CI) serves as an important building block for the synthesis of various organic compounds.

Explanation

The compound holds potential for a range of applications across different fields, including pharmaceuticals, materials science, and chemical research.

Derivative of Pyrrole

Yes

Structural Relationship

Bilirubin

Potential Applications

Organic Synthesis, Materials Science

Interest in Fields

Medicinal Chemistry, Biological Research

Importance

Building Block for Organic Compounds

Range of Applications

Different Fields

Check Digit Verification of cas no

The CAS Registry Mumber 453590-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,3,5,9 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 453590-50:
(8*4)+(7*5)+(6*3)+(5*5)+(4*9)+(3*0)+(2*5)+(1*0)=156
156 % 10 = 6
So 453590-50-6 is a valid CAS Registry Number.

453590-50-6Downstream Products

453590-50-6Relevant articles and documents

Structure and synthesis of the natural heptachloro-1′-methyl-1,2′-bipyrrole (Q1)

Wu, Jun,Vetter, Walter,Gribble, Gordon W.,Schneekloth Jr., John S.,Blank, David H.,Goerls, Helmar

, p. 1740 - 1743 (2002)

Which organism produces it? The natural product Q1 is 64 % chlorine and every third atom is a halogen, but the source of Q1 is unknown. Synthetic Q1, made for the first time, has identical chromatographic and spectroscopic properties to those of Q1 extracted from environmental samples.

Synthesis of 1,2′- and 1,3′-bipyrroles from 2- and 3-nitropyrroles

Fu, Liangfeng,Gribble, Gordon W.

, p. 3545 - 3548 (2008/09/21)

1,2′- and 1,3′-Bipyrroles, which are attractive precursors for the synthesis of bipyrrole-based natural products, are synthesized in one-pot from 2- and 3-nitropyrroles by a sequential nitro group reduction-Paal-Knorr pyrrole synthesis.

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