19429-86-8

Basic information

• Product Name: N,N-DiMethylpropionaMidediMethylacetale
• Synonyms: N,N-DiMethylpropionaMidediMethylacetale;N,N-Dimethylpropionamide Dimethyl Acetal;1,1-dimethoxy-N,N-dimethylpropan-1-amine
• CAS NO: 19429-86-8
• Molecular Formula: C₇H₁₇NO₂
• Molecular Weight: 147.21538
• Mol File: 19429-86-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 30 °C(Press: 12 Torr)
• Appearance: /
• Density: 0.897±0.06 g/cm3(Predicted)
• PKA: 5.08±0.50(Predicted)
• CAS DataBase Reference: N,N-DiMethylpropionaMidediMethylacetale(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-DiMethylpropionaMidediMethylacetale(19429-86-8)
• EPA Substance Registry System: N,N-DiMethylpropionaMidediMethylacetale(19429-86-8)

Safety Data

• Hazardous Substances Data: 19429-86-8(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 21511-56-8 trimethylpropionic imidinium methylsulfate 
• 67-56-1 methanol 
• 758-96-3 N,N-dimethyl-propanamide 

Downstream Products

• 52512-63-7 5-ethyl-3-trans-p-tolylazo-[1,2,4]oxadiazole 
• 52512-62-6 3-(4-chloro-trans-phenylazo)-5-ethyl-[1,2,4]oxadiazole 
• 112752-54-2 N,N-Dimethyl-N'-(4-methyl-benzyl)-propionamidine 
• 862207-45-2 (2R,4aS,8aS)-cis-2-[8-(4-methoxy-benzyloxymethyl)-4a-methyl-1,2,4a,8a-tetrahydronaphthalen-2-yl]-N,N-dimethylpropionamide 
• 1596358-18-7 (E)-N-[1-(dimethylamino)propylidene]-4-nitrobenzenecarbothioamide 
• 1315180-42-7 C₁₈H₂₁FN₂O₂ 
• 1315180-12-1 (E)-1-(4-bromo-2-fluorophenyl)-3-dimethylamino-2-penten-1-one 
• 107322-44-1 N'-(3-Ethoxy-phenyl)-N,N-dimethyl-propionamidine 
• 57058-36-3 N'-Benzyl-N,N-dimethyl-propionamidine 
• 112752-57-5 N'-Isopropyl-N,N-dimethyl-propionamidine 
• 107322-51-0 C₁₁H₁₅N₃O₂ 
• 107322-47-4 N'-(4-Chloro-phenyl)-N,N-dimethyl-propionamidine 
• 107322-43-0 N'-(3-Methoxy-phenyl)-N,N-dimethyl-propionamidine 

Relevant articles and documents

METHOD FOR THE PREPARATION OF 1-ARYL-1-ALKYL-2-ALKYL-3-DIALKYLAMINOPROPANE COMPOUNDS

The present invention refers to the preparation of 1-aryl-1-alkyl-2-alkyl-3-dialkylamino-propane compounds, such as tapentadol, using a diastereoselective Eschenmoser-Claisen or Ireland-Claisen rearrangement.

Process for preparation of adjacently disubstituted ketones

A novel 7-hydroxyprostaglandin E1, or a stereoisomer thereof, or a protected derivative thereof, having the following formula: STR1 wherein R8 represents H, CH3 or C2 H5, R9 represents H or CH3, R10 and R11 are identical or different, and each represents H, tetrahydropyranyl or t-butyldimethylsilyl. Also provided is a process for producing an adjacently disubstituted ketone including the above compounds, i.e. 7-oxoprostaglandin, etc. which comprises reacting an α,β-unsaturated carbonyl compound with a cuprous salt and an organolithium compound in an aprotic inert organic medium in the presence of trialkylphosphine, the amounts of said cuprous salt and said organolithium compound being substantially equimolar, and reacting the product with a protected acetal derivative of an organic carbonyl compound or an aldehyde in the presence of a Lewis acid, if necessary, followed by reacting the product with a proton donor.