7235-16-7

Basic information

• Product Name: 4-chloro-3-fluoro-2-methoxy-3-methylhex-4-enoic acid
• CAS NO: 7235-16-7
• Molecular Formula: C₁₃H₁₂O
• Molecular Weight: 210.6305
• Mol File: 7235-16-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 326.2°C at 760 mmHg
• Flash Point: 151.1°C
• Density: 1.222g/cm³
• Vapor Pressure: 4.41E-05mmHg at 25°C
• Refractive Index: 1.46
• CAS DataBase Reference: 4-chloro-3-fluoro-2-methoxy-3-methylhex-4-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-3-fluoro-2-methoxy-3-methylhex-4-enoic acid(7235-16-7)
• EPA Substance Registry System: 4-chloro-3-fluoro-2-methoxy-3-methylhex-4-enoic acid(7235-16-7)

Safety Data

• Hazardous Substances Data: 7235-16-7(Hazardous Substances Data)

Upstream product

• 628-20-6 4-Chlorobutyronitrile 
• 95-13-6 1-indene 
• 38425-61-5 β-1-(indanyl)butyric acid 
• 10409-13-9 3-(3'-bromopropyl)indene 
• 37848-93-4 3-(1H-inden-3-yl)propanol 
• 1271193-48-6 C₁₃H₁₂O 
• 1271192-90-5 2-(2-iodobenzyl)-3-oxocyclohex-1-enyl trifluoromethanesulfonate 
• 83-33-0 inden-1-one 
• 1620-02-6 1-Ethoxycarbonylmethyl-1-hydroxy-indan 
• 22339-45-3 2,3-dihydro-1H-indene-1-acetic acid ethyl ester 
• 38434-36-5 (2-indan-1-yl-ethyl)-malonic acid diethyl ester 
• 38425-60-4 Methyl-4-(1-indanyliden)-2-butenoat 
• 38434-37-6 1-(3-Methoxy-propyl)-indan-1-ol 
• 38434-39-8 1-(3-Methoxy-propyl)-indan 

Downstream Products

• 1730-37-6 1-methylfluorene 
• 7235-17-8 1-Oximino-1,2,3,4-tetrahydro-fluoren 
• 876726-06-6 1,2,3,4-tetrahydro-9H-1-[1-(phenylthio)cyclopropyl]fluoren-1-ol 

Relevant articles and documents

Stereoselective syntheses of spirane bridged semi-titanocenes

The synthesis of bidentate cyclopentadienyl-alkoxide ligands and their complexation to titanium are described. The focus has been on methodology for stereoselective synthesis of ansa half-sandwich titanocenes with rigid C 2- and C3-b

4a-Methyl-4aH-fluorenes

The monobenzo derivative (1) of 3a-methyl-3aH-indene and its methyl derivative (3) have been synthesised; although isolable they are reactive, undergoing autoxidation, dimerisation, and other cycloadditions, thermal and acid catalysed aromatisation to fluorenes, and photochemical rearrangement to naphthalenes.