7319-16-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
1-Methoxy-1-propene is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to facilitate the production of these compounds.
Used as a Solvent in Industrial Processes:
1-Methoxy-1-propene is used as a solvent in various industrial processes due to its ability to dissolve a wide range of substances and its compatibility with different materials.
Used in the Production of Other Chemicals:
1-Methoxy-1-propene is used as a precursor in the production of other chemicals such as 1-methoxy-2-propanol and 1-methoxy-2-propanone, contributing to the synthesis of these compounds.
Used as a Reagent in the Preparation of Aldehydes and Ketones:
1-Methoxy-1-propene is utilized as a reagent in the preparation of aldehydes and ketones, playing a crucial role in the synthesis of these organic compounds.
Safety Precautions:
Due to its potentially hazardous nature, proper precautions must be taken when handling 1-methoxy-1-propene to prevent exposure and ensure safety in its usage. This includes following safety guidelines and using appropriate protective equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 7319-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7319-16:
(6*7)+(5*3)+(4*1)+(3*9)+(2*1)+(1*6)=96
96 % 10 = 6
So 7319-16-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O/c1-3-4-5-2/h3-4H,1-2H3
7319-16-6Relevant academic research and scientific papers
Trends in alkyl substituent effects on nucleophilic reactions of carbonyl compounds: Gas phase reactions between ammonia and R1R2COCH3+ oxonium ions
Bache-Andreassen, Lihn,Uggerud, Einar
, p. 705 - 713 (2007/10/03)
The reactivity of carbonyl substituted methyl oxonium ions (R1R2COCH3-) towards ammonia has been investigated using an FT-ICR mass spectrometer and ab initio calculations. The monosubstituted ions (R1=H: R2 = H, CH3, C2H5 and i-C3H7) show different reaction patterns with variable degree of: (1) nucleophilic substitution, (2) addition elimination and (3) proton transfer, when reacted with ammonia. In all cases addition-elimination dominates over nucleophilic substitution, and the observed reactions are slow. The trends in reactivity are consistent with the alkyl group's electronic properties, as expressed by a single parameter linear or slightly non-linear model.
