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The chemical compound "methyl 3-{5-acetyl-2-[2-({3-ethyl-5-[(4-ethyl-3-methyl-2-oxo-2H-pyrrol-5-yl)methylidene]-4-methyl-1,5-dihydro-2H-pyrrol-2-ylidene}methyl)-3-methyl-4-oxo-4,5-dihydrocyclopenta[b]pyrrol-6(1H)-ylidene]-4-methyl-3,4-dihydro-2H-pyrrol-3-yl}propanoate" is a complex organic molecule with a long and intricate structure. It consists of a methyl ester group attached to a propanoic acid backbone, which is further connected to a complex heterocyclic system. This system includes a pyrrol ring with various substituents, such as acetyl, methyl, and ethyl groups, as well as a cyclopenta[b]pyrrol ring. The molecule also features a dihydro-2H-pyrrol-2-ylidene group and a 2-oxo-2H-pyrrol-5-ylmethylidene moiety, indicating a high degree of unsaturation and complexity. methyl 3-{5-acetyl-2-[2-({3-ethyl-5-[(4-ethyl-3-methyl-2-oxo-2H-pyrrol-5-yl)methylidene]-4-methyl-1,5-dihydro-2H-pyrrol-2-ylidene}methyl)-3-methyl-4-oxo-4,5-dihydrocyclopenta[b]pyrrol-6(1H)-ylidene]-4-methyl-3,4-dihydro-2H-pyrrol-3-yl}propanoate is likely to be of interest in the field of organic chemistry, potentially for its unique electronic properties or as a precursor in the synthesis of other complex molecules.

7234-29-9

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7234-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7234-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,3 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7234-29:
(6*7)+(5*2)+(4*3)+(3*4)+(2*2)+(1*9)=89
89 % 10 = 9
So 7234-29-9 is a valid CAS Registry Number.

7234-29-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-[5-acetyl-2-[2-[[3-ethyl-5-[(3-ethyl-4-methyl-5-oxopyrrol-2-yl)methylidene]-4-methylpyrrol-2-ylidene]methyl]-3-methyl-4-oxo-1H-cyclopenta[b]pyrrol-6-ylidene]-4-methyl-3,4-dihydropyrrol-3-yl]propanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:7234-29-9 SDS

7234-29-9Downstream Products

7234-29-9Relevant academic research and scientific papers

O-(p-Methoxyphenylethynyl)phenyl Glycosides: Versatile New Glycosylation Donors for the Highly Efficient Construction of Glycosidic Linkages

Hu, Yang,Yu, Ke,Shi, Li-Li,Liu, Lei,Sui, Jing-Jing,Liu, De-Yong,Xiong, Bin,Sun, Jian-Song

, p. 12736 - 12744 (2017/09/25)

A novel alkyne-activation-based glycosylation protocol using o-(p-methoxyphenylethynyl)phenyl (MPEP) glycoside was established. The glycosyl MPEP donors were shelf-stable and could be prepared efficiently via Sonogashira reaction from the corresponding o-

Probing the aglycon promiscuity of an engineered glycosyltransferase

Gantt, Richard W.,Goff, Randal D.,Williams, Gavin J.,Thorson, Jon S.

supporting information; experimental part, p. 8889 - 8892 (2009/05/26)

(Figure Presented) A sweet library: Two variants (wild-type (WT) and a triple mutant) of glycosyltransferase (GT) OleD have been shown to catalyze glycosylation of over 70 substrates, formation of O-, S- and N-glycosidic bonds, and iterative glycosylation (see scheme). Identified substrates include nucleophiles not previously known to act in GT reactions and span numerous natural product and therapeutic drug classes.

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