Chlorin e6 dimethylester

Product Number: C40814; CAS Number: 197444-89-6

$82.00$1,806.00

$82.00
$161.00
$477.00
$1,806.00

Chlorin e6 dimethylester CAS: 197444-89-6 MDL: MFCD32267982

Molecular weight: 624.73 g/mol

Molecular Formula: C36H40N4O6                        

CAS Number: 197444-89-6

Storage: Store at  room temperature, protect from light.

Synonyms: (17S,18S)-7-Ethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethyl-12-vinyl-17,18-dihydro-2-porphyrincarbonsäure, (17S,18S)-7-Ethyl-20-(2-methoxy-2-oxoethyl)-18-(3-methoxy-3-oxopropyl)-3,8,13,17-tetramethyl-12-vinyl-17,18-dihydro-2-porphyrincarboxylic acid, 21H,22H-Porphine-13-propanoic acid, 17-carboxy-7-ethenyl-2-ethyl-12,13-dihydro-15-(2-methoxy-2-oxoethyl)-3,8,12,18-tetramethyl-, α-methyl ester, (12S,13S)- ,Acide (17S,18S)-7-éthyl-20-(2-méthoxy-2-oxoéthyl)-18-(3-méthoxy-3-oxopropyl)-3,8,13,17-tétraméthyl-12-vinyl-17,18-dihydro-2-porphyrinecarboxylique

Field of Interest: Natural porphyrins, Chlorophyll Derivatives

Background: Chlorin e6 dimethylester is a chlorophyll derived natural chlorin specialty chemical derivative manufactured by Frontier Specialty Chemicals. Chlorin e6 dimethylester  is used a starting material for the synthesis of chlorin based photosensitizers.

References: 

1.) Hargus, et al. Mono-(L)-aspartylchlorin-e6 Photochemistry and Photobiology, 2007, vol. 83, # 5, p. 1006 – 1015. https://doi.org/10.1111/j.1751-1097.2007.00092.x

2.) Jinadasa, et al. Syntheses and cellular investigations of 173-, 152-, and 131-amino acid derivatives of chlorin e6. Journal of Medicinal Chemistry, 2011, vol. 54, # 21, p. 7464 – 7476. https://doi.org/10.1021/jm2005139

3.) Jalde, et al. Synthesis of novel Chlorin e6-curcumin conjugates as photosensitizers for photodynamic therapy against pancreatic carcinoma. European Journal of Medicinal Chemistry, 2018, vol. 147, p. 66 – 76. https://doi.org/10.1016/j.ejmech.2018.01.099

4.) Chen, et al. Syntheses and PDT activity of new mono- and di-conjugated derivatives of chlorin e6 . Journal of Porphyrins and Phthalocyanines, 2017, vol. 21, # 4-6, p. 354 – 363. https://doi.org/10.1142/S1088424617500262

5.) Zhang, et al. Design, synthesis and biological evaluation of novel 31-hexyloxy chlorin e6-based 152– or 131-amino acid derivatives as potent photosensitizers for photodynamic therapy. European Journal of Medicinal Chemistry, 2020, vol. 207, art. no. 112715. https://www.sciencedirect.com/science/article/abs/pii/S0223523420306875?via%3Dihub

6.) Gomi, et al. The Structures of Mono-L-aspartyl chlorin e6 and its Related CompoundsHeterocycles, 1998, vol. 48, # 11, p. 2231 – 2244. DOI: 10.3987/COM-98-8286

Categories

Functional Groups

, , ,

Porphyrin Family

Chlorophyll Derivatives

Porphyrin Substitution

Beta Substituted Porphyrins, Carboxy Substituted Porphyrins

Purity %

>95%

Molecular Formula

C36H40N4O6

Molecular Weight

624.726

CAS #

197444-89-6

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