Chlorin e6 dimethylester

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

  • Fast Global Shipping
  • Guaranteed Purity
  • Need smaller sizes or bulk? Contact us!
$82.00
$161.00
$477.00
$1,806.00
SKU: C40814 Category:

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 Compounds. Heterocycles, 1998, vol. 48, # 11, p. 2231 – 2244. DOI: 10.3987/COM-98-8286

Categories

Porphyrins

Scaffold/Subcategory

Natural Porphyrins and Derivatives

CAS #

[197444-89-6]

Purity %

>95%

Smiles

CCC1=C(C)C2=NC1=C/C1=C(C)C(C(O)=O)=C(N1)C(CC(=O)OC)=C1/N=C(/C=C3NC(=C2)/C(C=C)=C3C)[C@@H](C)[C@@H]1CCC(=O)OC

Molecular Weight

624.726

Molecular Formula

C36H40N4O6

Functional Groups

Carboxy, Carboxylic Acid, Ester, Vinyl

Porphyrin Family

Chlorophyll Derivatives, Free Base Porphyrins

Porphyrin Substitution

Alkyl Substituted Porphyrins, Beta Substituted Porphyrins, Carboxy Substituted Porphyrins

You may also like…

Shopping Cart
Scroll to Top