51732-61-7

Basic information

• Product Name: 7C-aglycone
• Synonyms: 7C-aglycone;vitamin K1 aglycone I
• CAS NO: 51732-61-7
• Molecular Formula: C18H18O4
• Molecular Weight: 298.33
• Mol File: 51732-61-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 497.4°C at 760 mmHg
• Flash Point: 268.7°C
• Appearance: /
• Density: 1.209g/cm³
• Vapor Pressure: 1.03E-10mmHg at 25°C
• Refractive Index: 1.575
• CAS DataBase Reference: 7C-aglycone(CAS DataBase Reference)
• NIST Chemistry Reference: 7C-aglycone(51732-61-7)
• EPA Substance Registry System: 7C-aglycone(51732-61-7)

Safety Data

• Hazardous Substances Data: 51732-61-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C18H18O4/c1-11(8-10-16(19)20)7-9-13-12(2)17(21)14-5-3-4-6-15(14)18(13)22/h3-7H,8-10H2,1-2H3,(H,19,20)/b11-7+

Upstream product

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• 53585-95-8 methyl (E)-6-hydroxy-4-methylhex-4-enoate 
• 66855-23-0 trans-1-Acetoxy-4-hydroxy-2-methyl-3-(5',5'-diethoxycarbonyl-3'-methyl-2'-pentenyl)-naphthalene 
• 99347-99-6 3-(5-carbomethoxy-3-methyl-(2E)-penten-yl)-1,4-dimethoxy-2-methylnaphthalene 
• 32247-33-9 2-prenyl-3-methyl-1,4-dimethoxynaphthalene 
• 99347-76-9 [1-(1,4-Dimethoxy-3-methyl-naphthalen-2-ylmethyl)-2-methyl-allylsulfanyl]-acetic acid methyl ester 
• 32659-14-6 4-bromo-3-methyl-2-buten-1-ol acetate 
• 66855-36-5 (E)-diethyl 2-(4-acetoxy-2-methylbut-2-en-1-yl)malonate 
• 6138-90-5 trans-geranyl bromide 
• 7421-23-0 trans-2-methyl-3-(3′,7′-dimethylocta-2′,6′-dienyl)-1,4-naphthoquinone 
• 58-27-5 menadione 
• 97804-50-7 1,4,4a,9a-tetrahydro-4a-methyl-(1α,4α,4aα,9aα)-1,4-methanoanthracene-9,10-dione 
• 67884-59-7 methyl (E)-4-methyl-6-bromohex-4-eneoate 
• 34207-04-0 NaQuinate-Me 

Relevant articles and documents

ANTICOAGULANT COMPOUNDS AND THEIR USE

According to the invention there is provided a compound of formula (I): wherein R1, R2, R3 and n have meanings given in the description, or a pharmaceutically acceptable solvate, salt or prodrug thereof for use as an anticoagulant.

Regio- and stereoselective terminal allylic carboxymethylation of gem-dimethyl olefins. Synthesis of biologically important linear degraded terpenoids

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Ubiquinone and related compounds. XXVII. Synthesis of urinary metabolites of phylloquinone and α tocopherol

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