1-ethenyl-4-(1-ethoxyethoxy)benzene | CAS:157057-20-0

We serve 1-ethenyl-4-(1-ethoxyethoxy)benzene CAS:157057-20-0 to global customers since 2007, Pls send inquiry to info@nbinno.com or visit www.nbinno.com our official website should you have any interests. This site is for information only.
1-ethenyl-4-(1-ethoxyethoxy)benzene

Synonyms:
1-(1-ethoxyethoxy)-4-vinylbenzene
Benzene, 1-ethenyl-4-(1-ethoxyethoxy)-
 
Molecular Formula:  C12H16O2
Molecular weight: 192.25400

Density: 0.983g/cm3
Boiling point: 286.517ºC at 760 mmHg
Flash point: 108.705ºC
Refractive index: 1.52
Vapor pressure: 0.005mmHg at 25°C

Items of Analysis Standard of Analysis Test Results
Appearance Colorless to light yellow liquid Conforms
Assay ≥98.0% 98.41%
Conclusion Conforms to Factory Standard
 



Contact us for information like 1-ethenyl-4-(1-ethoxyethoxy)benzene chemical properties,Structure,melting point,boiling point,density,molecular formula,molecular weight,Benzene, 1-ethenyl-4-(1-ethoxyethoxy)- physical properties,toxicity information,customs codes,safety, risk, hazard and MSDS, CAS,cas number,1-ethenyl-4-(1-ethoxyethoxy)benzene Use and application,1-ethenyl-4-(1-ethoxyethoxy)benzene technical grade,usp/ep/jp grade.


Related News: Bristol-Myers Squibb (BMS) recently acquired Celgene, for example, which had the highest proportional R&D spend.6-methyl-7-nitro-quinoxaline-2,3-dione-5-hydrazide manufacturer “Standard respiratory support therapies are used to treat the symptoms and wait for the virus to be cleared by itself.”1-(4-chloro-phenyl)-5-formyl-1H-pyrazole-3-carboxylic acid ethyl ester supplier DMF is the main management method for APIs in developed countries in Europe and the United States. Under the DMF system, API companies can submit DMF filing documents to the regulatory authority at any time, but the regulatory authority will not conduct technical reviews on them. When the drug is administered, the regulatory authority will associate and review the drug substance and the preparation.2α-Brom-3β-hydroxy-4,4-dimethyl-cholest-5-en vendor DMF is the main management method for APIs in developed countries in Europe and the United States. Under the DMF system, API companies can submit DMF filing documents to the regulatory authority at any time, but the regulatory authority will not conduct technical reviews on them. When the drug is administered, the regulatory authority will associate and review the drug substance and the preparation.High-barrier generic drugs: Usually for the production of drugs whose patents have just expired or are about to expire, the market is only competed by original research and a few generic drug companies.