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The chemical compound "1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-4-ethyl-3-methyl-1H-pyrrol-2-yl]methyl]-4-ethyl-3-methyl, phenylmethyl ester" is a complex organic molecule with a molecular formula of C26H33NO4. It is a derivative of 1H-pyrrole-2-carboxylic acid, featuring a pyrrole ring with various substituents. The compound has a 5-[(1,1-dimethylethoxy)carbonyl]-4-ethyl-3-methyl-1H-pyrrol-2-yl]methyl group attached to the pyrrole ring, which is further connected to a 4-ethyl-3-methyl-1H-pyrrole-2-carboxylic acid moiety. The molecule is esterified with phenylmethyl (benzyl) group, making it a phenylmethyl ester. 1H-Pyrrole-2-carboxylic acid, 5-[[5-[(1,1-dimethylethoxy)carbonyl]-4-ethyl-3-methyl-1H-pyrrol-2-yl]meth yl]-4-ethyl-3-methyl-, phenylmethyl ester is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex organic molecules.

52459-98-0

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52459-98-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52459-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,5 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52459-98:
(7*5)+(6*2)+(5*4)+(4*5)+(3*9)+(2*9)+(1*8)=140
140 % 10 = 0
So 52459-98-0 is a valid CAS Registry Number.

52459-98-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 5-((5-(tert-butoxycarbonyl)-4-ethyl-3-methyl-1H-pyrrol-2-yl)methyl)-4-ethyl-3-methyl-1H-pyrrole-2-carboxylate

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:52459-98-0 SDS

52459-98-0Relevant academic research and scientific papers

Total synthesis of the porphyrin mineral abelsonite and related petroporphyrins with five-membered exocyclic rings

Zhang, Bo,Lash, Timothy D.

, p. 7253 - 7256 (2007/10/03)

A reliable synthesis of porphyrins with five-membered exocyclic rings from b-bilenes has been developed. This methodology has been applied to the first total synthesis of the porphyrin mineral abelsonite, as well as the widespread petroporphyrin deoxophyl

Synthesis and Characterisation of the C30-De-ethylaetioporphyrin Present in Petroleum

Clewlow, Paul J.,Jackson, Anthony H.

, p. 1925 - 1936 (2007/10/02)

The four de-ethyl analogues of the relatively ubiquitous and biogenetically significant petroporphyrin aetioporphyrin III (3a-d) have been synthesized utilising the ac-biladiene route.A reversed-phase HPLC method of separating a mixture of the four synthe

Synthesis of the C30 Desethylaetioporphyrin from Petroleum

Clewlow, Paul J.,Jackson, Anthony H.,Roberts, Ian

, p. 724 - 726 (2007/10/02)

The four desethyl analogues of aetioporphyrin-III have been synthesised by the biladiene route; h.p.l.c. comparisons showed that the desethylaetioporphyrin obtained from petroleum is the c-ring isomer (3c).

BILE PIGMENT STUDIES-VI. SYNTHESES OF MODEL SYSTEMS

Smith, Kevin M.,Kishore, Dharma

, p. 1841 - 1848 (2007/10/02)

The synthesis of various mammalian and algal bile pigment models from monopyrroles and by ring cleavage of intact metalloporphyrins and metallochlorins is discussed.A previously reported synthesis of etiobiliverdin IVγ (6) from the self-condensation of a

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