7462-75-1

Basic information

• Product Name: 2-chloro-2-methylpropanamide
• CAS NO: 7462-75-1
• Molecular Formula: C₄H₈ClNO
• Molecular Weight: 121.5654
• Mol File: 7462-75-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 237.1°C at 760 mmHg
• Flash Point: 97.2°C
• Density: 1.138g/cm³
• Vapor Pressure: 0.0457mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: 2-chloro-2-methylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-2-methylpropanamide(7462-75-1)
• EPA Substance Registry System: 2-chloro-2-methylpropanamide(7462-75-1)

Safety Data

• Hazardous Substances Data: 7462-75-1(Hazardous Substances Data)

Upstream product

• 594-61-6 2-methyllactic acid 
• 76170-90-6 methyl ester of α-(N-chloro-N-methoxyamino)isobutyric acid 
• 19444-33-8 2-chloroethyl 2-chloro-2-methylpropionate 
• 22421-97-2 methyl 2-chloroisobutyrate 
• 13222-26-9 2-chloroisobutyryl chloride 

Downstream Products

• 3331-60-0 chloroisobutyronitrile 
• 2310-98-7 2-bromo-2-chloropropane 
• 6552-42-7 N-bromo-2-chloro-2-methyl-propionamide 
• 3017-95-6 2-bromo-1-chloropropane 
• 594-61-6 2-methyllactic acid 
• 67-64-1 acetone 

Relevant articles and documents

Asymmetric auto-tandem catalysis with a planar-chiral ruthenium complex: Sequential allylic amidation and atom-transfer radical cyclization

Ru does it all: A novel example of an asymmetric auto-tandem reaction catalyzed by a planar-chiral cyclopentadienyl-ruthenium complex is described. The reaction of allylic chloride with α-haloamides provides synthetically useful, diastereomerically and enantiomerically enriched γ-lactams with multiple stereogenic centers through one-pot sequential allylic amidation/atom-transfer radical cyclization. PG=protecting group. Copyright

GEMINAL SYSTEMS. 16. REACTIONS OF N-CHLORO-N-ALKOXY-N-ALKYLANINES WITH AMINES

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