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| 2-Methoxypropene Basic information |
| 2-Methoxypropene Chemical Properties |
Melting point | 25°C | Boiling point | 34-36 °C (lit.) | density | 0.753 g/mL at 25 °C (lit.) | vapor pressure | 27.96 psi ( 55 °C) | refractive index | n20/D 1.382(lit.) | Fp | −21 °F | storage temp. | 2-8°C | solubility | Chloroform | form | Liquid | color | Clear colorless | PH | 7 (H2O) | Water Solubility | negligible | Sensitive | Light Sensitive | BRN | 1734635 | LogP | 1.7 at 21℃ and pH8.1-8.4 | CAS DataBase Reference | 116-11-0(CAS DataBase Reference) | NIST Chemistry Reference | 1-Propene, 2-methoxy-(116-11-0) | EPA Substance Registry System | 1-Propene, 2-methoxy- (116-11-0) |
Hazard Codes | F+,Xn,F | Risk Statements | 12-19-22-11 | Safety Statements | 3-16-29-33-7/9-9-18 | RIDADR | UN 1993 3/PG 1 | WGK Germany | 1 | RTECS | UD0800000 | F | 8-10 | Autoignition Temperature | 374 °F | TSCA | Yes | HazardClass | 3 | PackingGroup | I | HS Code | 29091990 | Hazardous Substances Data | 116-11-0(Hazardous Substances Data) | Toxicity | rabbit,LD50,skin,> 20mL/kg (20mL/kg),American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969. |
| 2-Methoxypropene Usage And Synthesis |
Chemical Properties | clear colorless liquid | Uses | 2-Methoxypropene is used in the synthesis of Macrolactin A, a 24-member macrolide typically employed as an antibiotic. Also used in the synthesis of phenylalanine derivatives used as α4β1 and α4β7 receptor antagonists in the treatment of allergic asthma. |
| 2-Methoxypropene Preparation Products And Raw materials |
Raw materials | Ethanone, 1-(3-methoxy-2,3-dimethyl-2-oxetanyl)- (9CI)-->Butanoic acid, 2,2,3,3,4,4,4-heptafluoro-, 1,1-dimethylethyl ester-->Butaneperoxoic acid, 2,2,3,3,4,4,4-heptafluoro-, 1,1-dimethylethyl ester-->2,3-Butanedione-->1,2-Diphenylethane-->Dimethyl carbonate-->Allene-->Pyridine-->2,2-Dimethoxypropane-->Methyl bromide-->Methyltriphenylphosphonium bromide | Preparation Products | Teprenone Impurity 20-->Warfarin-->1,3-Dioxan-5-ol, 2,2-dimethyl--->1,2:5,6-Bis-O-(1-methylethylidene)-D-mannitol-->5-KETOHEXANENITRILE-->4-(CHLOROMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE |
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