6180-67-2

Basic information

• Product Name: ALLYLOXY PROPANOL
• Synonyms: ALLYLOXY PROPANOL
• CAS NO: 6180-67-2
• Molecular Formula: C₆H₁₂O₂
• Molecular Weight: 116.16
• Mol File: 6180-67-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 186.0±15.0 °C(Predicted)
• Appearance: /
• Density: 0.917±0.06 g/cm3(Predicted)
• PKA: 14.92±0.10(Predicted)
• CAS DataBase Reference: ALLYLOXY PROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYLOXY PROPANOL(6180-67-2)
• EPA Substance Registry System: ALLYLOXY PROPANOL(6180-67-2)

Safety Data

• Statements: 10-36/37/38
• Safety Statements: 16-26-36/37/39
• RIDADR: 1987
• Hazardous Substances Data: 6180-67-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 107-18-6 allyl alcohol 

Downstream Products

• 30359-45-6 3-[2-chloro-3-(3-chloro-o-tolyl)propoxy]propanol 
• 504-63-2 trimethyleneglycol 
• 858355-56-3 7-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosylthio)-4-oxaheptyl p-toluenesulfonate 
• 22577-15-7 3-(allyloxy)propionic acid 
• 125947-55-9 1-[(6aS,11bS)-3-(3-Allyloxy-propyl)-7-benzyl-2,3,5,6,6a,7-hexahydro-1H-pyrrolo[2,3-d]carbazol-4-yl]-ethanone 
• 125947-52-6 1-[(3aS,6aS,11bS)-3-(3-Allyloxy-propyl)-7-benzyl-2,3,3a,4,5,6,6a,7-octahydro-1H-pyrrolo[2,3-d]carbazol-4-yl]-ethanone 
• 125947-54-8 (6aS,11bS)-3-(3-Allyloxy-propyl)-7-benzyl-5,6,6a,7-tetrahydro-3H-pyrrolo[2,3-d]carbazol-2-one 
• 142288-06-0 3-(allyloxy)propyl 4-methylbenzenesulfonate 
• 44768-60-7 3-allyloxypropionaldehyde 
• 1062643-13-3 C₃₉H₄₂F₅N₃O₆ 
• 557-40-4 Allyl ether 
• 28485-79-2 1,3-bis(allyloxy)propane 
• 77757-02-9 3-allyloxypropyl methacrylate 
• 172147-69-2 (2S,3S,4R,5R,6S)-2-[(1R,2R)-2-(3-Allyloxy-propoxy)-cyclohexyloxy]-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran 

Relevant articles and documents

PRODUCTION PROCESS OF 3-ALKOXY-1-PROPANOLS, AND 3-ALKOXY-1-PROPANOLS OBTAINED BY THE PRODUCTION PROCESS

In the presence of a catalyst containing at least one element selected from the group consisting of elements of the group III, lanthanoid elements and actinoid elements of the Periodic Table, an allyl alcohol is reacted with an alcohol compound. A method for efficiently producing 3-alkoxy-1-propanol in a single step using an alcohol as a starting material is provided.