251912-48-8

Basic information

• Product Name: [5-(benzyloxy)-1,3-phenylene]dimethanol
• Synonyms: [5-(benzyloxy)-1,3-phenylene]dimethanol
• CAS NO: 251912-48-8
• Molecular Weight: 244.29
• Mol File: 251912-48-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: [5-(benzyloxy)-1,3-phenylene]dimethanol(CAS DataBase Reference)
• NIST Chemistry Reference: [5-(benzyloxy)-1,3-phenylene]dimethanol(251912-48-8)
• EPA Substance Registry System: [5-(benzyloxy)-1,3-phenylene]dimethanol(251912-48-8)

Safety Data

• Hazardous Substances Data: 251912-48-8(Hazardous Substances Data)

Upstream product

• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 100-51-6 benzyl alcohol 
• 53478-04-9 dimethyl 5-(benzyloxy)isophthalate 
• 100-39-0 benzyl bromide 
• 39630-68-7 diethyl 5-hydroxyisophthalate 
• 251912-45-5 5-benzyloxy-isophthalic acid diethyl ester 

Downstream Products

• 1161868-12-7 C₂₅H₂₄O₇ 
• 1161867-70-4 C₃₅H₃₂O₁₁ 
• 894094-41-8 {3-[3-benzyloxy-5-(3,5-bis-hydroxymethyl-phenoxymethyl)-benzyloxy]-5-hydroxymethyl-phenyl}-methanol 
• 1161867-80-6 C₆₃H₅₆O₁₅ 
• 1161867-78-2 C₅₅H₄₈O₇ 
• 894094-40-7 C₃₉H₄₀O₁₁ 
• 1027755-92-5 1-benzyloxy-3,5-bis(chloromethyl)benzene 
• 251912-33-1 O-benzyl-3,5-bis(phenylthiomethyl)phenol 
• 522609-24-1 O-benzyl-3,5-di(formyl)phenol 

Relevant articles and documents

PHOSPHATE DERIVATIVES AND USE THEREOF

The present invention discloses a compound with the following formula (I), or a tautomer, mesomer, racemate, enantiomer, and diastereoisomer thereof, or a mixture form thereof, or a pharmaceutically acceptable salt thereof, or a prodrug molecule thereof, wherein D is selected from: The invention further discloses the use of the compound in the preparation of drugs for preventing and/or treating cancers, and the use of the compound in the preparation of drugs for inhibiting cancer metastasis. The compound of the present invention can effectively inhibit the proliferation and metastasis of cancer cells by adjusting the acidity of a tumor microenvironment to achieve a better effect in clinical cancer treatment, and has broad application prospects.

Artificial transcription factors which mediate double-strand DNA Cleavage

A new family of artificial transcription factor (ATF)-based conjugates have been designed and synthesized as potent chemical nucleases. Polyamides as the important and efficient ATFs were used to modify and activate several anchor compounds. The results demonstrate that the resulting conjugates remarkably promote the rate accelerations and non-random double-strnd DNA cleavage activity. Interestingly, the cleavage activity of both the hydrolytic and oxidative agents was promoted efficiently through the modification of the ATFs.

Pyridinium N-heteroarylaminides: synthesis of N-heteroarylpolyamines

The synthesis of a set of new N-heteroarylpolyamines is reported. A multiple and regioselective alkylation on the exo nitrogen of pyridinium N-(heteroaryl)aminides with several polybromo compounds, followed by a clean N-N bond reduction of the corresponding pyridinium salts, provides an easy and general method to obtain the title compounds.