170508-51-7

Basic information

• Product Name: 2,5-Bis<(2-methoxyethoxy)methoxy>benzaldehyde
• Synonyms: 2,5-Bis<(2-methoxyethoxy)methoxy>benzaldehyde
• CAS NO: 170508-51-7
• Molecular Weight: 314.335
• Mol File: 170508-51-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,5-Bis<(2-methoxyethoxy)methoxy>benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Bis<(2-methoxyethoxy)methoxy>benzaldehyde(170508-51-7)
• EPA Substance Registry System: 2,5-Bis<(2-methoxyethoxy)methoxy>benzaldehyde(170508-51-7)

Safety Data

• Hazardous Substances Data: 170508-51-7(Hazardous Substances Data)

Upstream product

• 1194-98-5 2,5-Dihydroxybenzaldehyde 
• 3970-21-6 2-Methoxyethoxymethyl chloride 

Downstream Products

• 144320-51-4 3-[(5Z,10Z,14Z,19Z)-(7S,8R)-8-[3-(2,5-Dihydroxy-phenyl)-propoxy]-18-(2-methoxycarbonyl-ethyl)-7-methoxycarbonylmethyl-3,7,12,17-tetramethyl-7,8,21,23-tetrahydro-porphin-2-yl]-propionic acid methyl ester 
• 170508-53-9 Methyl 3-<2,5-bis<(2-methoxyethoxy)methoxy>phenyl>propanoate 
• 170508-54-0 3-<2,5-Bis<(2-methoxyethoxy)methoxy>phenyl>-1-propanol 
• 144320-50-3 1-<2,5-Bis<(2-methoxyethoxy)methoxy>phenyl>-3-bromopropane 
• 170508-52-8 Methyl (2E)-3-<2,5-bis<(2-methoxyethoxy)methoxy>phenyl>acrylate 

Relevant articles and documents

Synthesis of Oxochlorins from the Red Blood Pigment Heme and Their Transformation into Potentially Biologically Active Chlorin Derivatives

The hydrochlorin rac-3 was prepared from the readily accessible chlorins rac-5a, b.The alcohol function of rac-3 could be used to attach an estrogen residue 28 and the hydroquinone 19 to yield the chlorin estrogen ethers 32a, b and the chlorin hydroquinone ether rac-30 respectively.The prepared chlorin estrogen derivatives might be useful as sensitizers and fluorescence markers for photodynamic therapy and other diagnostic/therapeutic applications.The chlorin hydroquinone ether is of interest as a potential artificial photosynthesis system, which contains a "natural" chlorin as a structural subunit in contrast to previously synthesized model systems based on porphyrins. - Keywords: Porphyrins / Chlorins / Estradiols / Quinones / Tumor therapy, photodynamic