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2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole is a complex organic compound characterized by a long hydrocarbon chain and multiple pyrrole rings. Its molecular structure features both pyrrolylmethylene and methoxy groups, which confer a distinctive combination of aromatic and aliphatic properties. 2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole is anticipated to exhibit a range of chemical and biological activities, making it a candidate for various applications such as a ligand or precursor in organic synthesis, or as a potential drug candidate due to its intricate structure and potential reactivity.

13129-81-2

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13129-81-2 Usage

Uses

Used in Organic Synthesis:
2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole is used as a ligand or precursor for its unique molecular structure, which can facilitate the creation of new organic compounds with specific properties.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole is used as a potential drug candidate. Its complex structure and potential reactivity suggest that it may have therapeutic applications that require further research and analysis to fully understand its chemical and biological properties.
Used in Chemical Research:
2-(5-Undecyl-2-pyrrolylmethylene)-3-methoxy-5-(2-pyrrolyl)-2H-pyrrole is utilized in chemical research to explore its diverse chemical and biological activities, which could lead to the development of new materials or processes.

Check Digit Verification of cas no

The CAS Registry Mumber 13129-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13129-81:
(7*1)+(6*3)+(5*1)+(4*2)+(3*9)+(2*8)+(1*1)=82
82 % 10 = 2
So 13129-81-2 is a valid CAS Registry Number.

13129-81-2Downstream Products

13129-81-2Relevant academic research and scientific papers

Pyrrole-Type compounds, compositions, and methods for treating cancer or viral diseases

-

, (2008/06/13)

The present invention relates to novel Pyrrole-Type compounds, compositions comprising Pyrrole-Type compounds, and methods useful for treating or preventing cancer or a neoplastic disorder comprising administering a composition comprising a Pyrrole-Type compound. The compounds, compositions, and methods of the invention are also useful for inhibiting the growth of a cancer cell or neoplastic cell. The present invention also relates to novel Pyrrole-Type compounds, compositions, and methods useful for treating or preventing a viral infection. The compounds, compositions, and methods of the invention are also useful for inhibiting the replication and/or infectivity of a virus.

Pyrrole-type compounds, compositions, and methods for treating cancer or viral diseases

-

, (2008/06/13)

The present invention relates to novel Pyrrole-Type compounds, compositions comprising Pyrrole-Type compounds, and methods useful for treating or preventing cancer or a neoplastic disorder comprising administering a composition comprising a Pyrrole-Type compound. The compounds, compositions, and methods of the invention are also useful for inhibiting the growth of a cancer cell or neoplastic cell. The present invention also relates to novel Pyrrole-Type compounds, compositions, and methods useful for treating or preventing a viral infection. The compounds, compositions, and methods of the invention are also useful for inhibiting the replication and/or infectivity of a virus.

Pyrrole-singlet oxygen reactions leading to α,α'-bipyrroles. Synthesis of prodigiosin and analogs

Wasserman, Harry H.,Petersen, Anders K.,Xia, Mingde,Wang, Jianji

, p. 7587 - 7589 (2007/10/03)

Reaction of the tert-butyl ester of 3-methoxy-2-pyrrolecarboxylic acid with singlet oxygen yields a hydroperoxide intermediate which undergoes coupling with pyrroles to yield precursors of prodigiosin and ring A analogs, readily convertible to the corresponding tripyrromethenes.

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