926-04-5

Basic information

• Product Name: 3,3-dimethylbutanamide
• Synonyms: 3,3-dimethylbutanamide;3,3-Dimethylbutyramide
• CAS NO: 926-04-5
• Molecular Formula: C₆H₁₃NO
• Molecular Weight: 115.17
• Mol File: 926-04-5.mol
• Article Data: 1

Chemical Properties

• Melting Point: 132-132.6 °C
• Boiling Point: 223.4°Cat760mmHg
• Flash Point: 88.9°C
• Appearance: /
• Density: 0.896g/cm³
• Vapor Pressure: 0.0963mmHg at 25°C
• Refractive Index: 1.433
• PKA: 16.79±0.40(Predicted)
• CAS DataBase Reference: 3,3-dimethylbutanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-dimethylbutanamide(926-04-5)
• EPA Substance Registry System: 3,3-dimethylbutanamide(926-04-5)

Safety Data

• Hazardous Substances Data: 926-04-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H13NO/c1-6(2,3)4-5(7)8/h4H2,1-3H3,(H2,7,8)

Upstream product

• 21954-81-4 ethyl t-butylcyanoacetate 
• 20669-05-0 2,2,4,4-tetramethyl-hexan-3-one 
• 71-43-2 benzene 
• 861523-94-6 2,2-dimethyl-1-[1]naphthyl-butan-1-one 
• 108-88-3 toluene 
• 861546-41-0 2,2-dimethyl-1-[2]naphthyl-butan-1-one 
• 263758-55-0 C₅₁H₅₉N₃O₅ 
• 263758-54-9 C₅₀H₅₅N₃O₅ 
• 263758-52-7 C₅₄H₅₈N₄O₅ 

Downstream Products

• 594-39-8 2-methyl-2-butylamine 
• 19656-71-4 N,N'-di-tert-pentyl-urea 
• 15673-00-4 3,3-dimethylbutylamine 
• 20654-46-0 2,2-dimethylbutyronitrile 
• 829-10-7 2,2-dimethyl-1-phenylbutanone 
• 1762-19-2 2,2-dimethyl-heptan-4-one 
• 1620693-41-5 C₁₁H₁₇NO₂S 
• 3302-16-7 3,3-dimethyl-butyronitrile 

Relevant articles and documents

CHEMICAL CONSTRUCTS

The invention provides a chemical construct for use in solid phase synthesis comprising a solid support Q having linked thereto via a connecting group Y a substrate R; the connecting group Y having first and second cleavage sites which are orthogonally and selectively cleavable; the second cleavage site being selectively cleavable to release the substrate; and the first cleavage site being located at a position between the second cleavage site and the solid support and being selectively cleavable to release a fragment Fr comprising the substrate and at least a portion of the connecting group Y; characterised in that cleavage at the first cleavage site forms or introduces on the chemical fragment Fr at the first cleavage site a moiety comprising a sensitising group G (such as an amino group) which sensitises the chemical fragment Fr to instrumental, e.g. mass spectroscopic, analysis. Also provided are methods of analysis employing the constructs, as well as intermediate constructs.