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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-[18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid;dihydrochloride

CCC1=C(C)/C/2=C/c3[nH]c(c(c3CC)C)/C=C/3N=C(/C=c/4[nH]/c(=CC1=N2)/c(C)c4CCC(=O)O)C(=C3C)CCC(=O)O.Cl.Cl Request for Quotation
Chemical Name: 3-[18-(2-carboxyethyl)-8,13-diethyl-3,7,12,17-tetramethyl-22,23-dihydroporphyrin-2-yl]propanoic acid;dihydrochloride
CAS Number: 68938-72-7
Product Number: AG00IBVW(AGN-PC-0JLI56)
Synonyms:
MDL No:
Molecular Formula: C34H40Cl2N4O4
Molecular Weight: 639.6118

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7,12-Diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid dihydrochloride is a versatile compound widely used in chemical synthesis as a catalyst for various reactions. Its unique molecular structure makes it particularly valuable in organic chemistry applications, where it serves as a powerful tool for promoting specific transformations.In chemical synthesis, this compound has been employed in the preparation of complex molecules such as pharmaceuticals, natural products, and functional materials. Its porphyrin structure facilitates the activation of substrates through coordination chemistry, enabling selective bond formations and modifications. By acting as a catalyst, it accelerates reaction rates and enhances product yields, making it an essential component in many synthetic routes.Furthermore, the dihydrochloride form of this compound provides enhanced stability and solubility in aqueous environments, broadening its utility in various synthetic protocols. Its ability to selectively bind to specific substrates and guide reaction pathways makes it a valuable asset for chemists seeking to streamline their synthetic procedures and obtain desired products efficiently.Overall, 7,12-Diethyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropionic acid dihydrochloride plays a crucial role in chemical synthesis by facilitating complex reactions, improving selectivity, and increasing the efficiency of synthetic processes. Its versatile applications make it an indispensable tool for researchers and chemists working in diverse fields of organic chemistry.