401894-76-6

Basic information

• Product Name: Carbamic acid, [2-(phenylmethoxy)-1,1-bis[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester
• CAS NO: 401894-76-6
• Molecular Formula: C30H37NO5
• Molecular Weight: 491.627
• Mol File: 401894-76-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(phenylmethoxy)-1,1-bis[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(phenylmethoxy)-1,1-bis[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(401894-76-6)
• EPA Substance Registry System: Carbamic acid, [2-(phenylmethoxy)-1,1-bis[(phenylmethoxy)methyl]ethyl]-, 1,1-dimethylethyl ester(401894-76-6)

Safety Data

• Hazardous Substances Data: 401894-76-6(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 146651-71-0 N-(tert-butyloxycarbonyl)-2-amino-2-(hydroxymethyl)propane-1,3-diol 

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.

Synthesis of Lower rim polyhydroxylated calix[4]arenes

Several synthetic procedures were evaluated and a protective/deprotective method, which allows the introduction of two, three, and four amide-linked polyhydroxylated units (TRIS) at the lower rim of calix[4]arenes was developed. Di- and trifunctionalized derivatives are poorly soluble in water, whereas the solubility of calix[4]arene having four polyhydroxylated amide groups is good (6 × 10-3 M at 25 °C).