17701-31-4

Basic information

• Product Name: 2,2-Dimethylhexanoyl chloride
• Synonyms: 2,2-Dimethylhexanoyl chloride
• CAS NO: 17701-31-4
• Molecular Formula: C₈H₁₅ClO
• Molecular Weight: 0
• Mol File: 17701-31-4.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2-Dimethylhexanoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-Dimethylhexanoyl chloride(17701-31-4)
• EPA Substance Registry System: 2,2-Dimethylhexanoyl chloride(17701-31-4)

Safety Data

• Hazardous Substances Data: 17701-31-4(Hazardous Substances Data)

Upstream product

• 813-69-4 2,2-dimethyl-hexanoic acid methyl ester 
• 20923-67-5 2,2-dimethyl-2-butyl acetamide 
• 55897-65-9 2,2-dimethylhexanenitrile 
• 813-72-9 2,2-dimethylhexanoic acid 

Downstream Products

• 39746-15-1 dimethyl (3,3-dimethyl-2-oxoheptyl)phosphonate 
• 15118-64-6 2,2-dimethyl-hexanoic acid anilide 
• 20923-67-5 2,2-dimethyl-2-butyl acetamide 

Relevant articles and documents

METAL COMPLEX, COMPOSITION AND LIGHT EMITTING DEVICE

A metal complex represented by formula (1) is provided. In formula (1), X represents a nitrogen atom or a group represented by ═C(RX)—; R1 represents an alkyl group having 4 or more carbon atoms; R2 represents an alkyl, cycloalkyl, alkoxy, cycloalkoxy, aryl, aryloxy, monovalent heterocyclic, or substituted amino group or a halogen atom; rings A and B each independently represent an aromatic hydrocarbon ring or an aromatic heterocyclic ring; M represents a rhodium, palladium, iridium, or platinum atom; n1 represents an integer of 1 or more, n2 represents an integer of 0 or more, and n1+n2 is 2 or 3; A1-G1-A2 represents an anionic bidentate ligand; A1 and A2 each independently represent a carbon atom, an oxygen atom, or a nitrogen atom; and G1 represents a single bond or an atomic group constituting a bidentate ligand together with A1 and A2.

Palladium-Catalyzed β-Mesylation of Simple Amide via Primary sp3 C-H Activation

A β-mesylation of primary sp3 C-H bonds from simple amides with methanesulfonic anhydride (Ms2O) has been established successfully at 80 °C in a Pd(OAc)2 (catalyst)/K2S2O8 (oxidant)/CF3CH2OH (solvent) system. These amide substrates involve N-monosubstituted linear, branch, or cyclic alkanes, and electron-deficient benzyl compounds. The β-mesylated amide products can be converted easily to β-fluoroamides or β-lactams through inter- or intramolecular SN2 processes.

PRODUCTION METHOD OF 1, 2, 4-TRIAZOLE COMPOUND

A method for producing a 1,2,4-triazole compound involves reacting an amide compound represented by formula (2) with a hydrazide compound represented by formula (3) in a solvent in the presence of a Lewis acid and a Lewis base, thereby obtaining a 1,2,4-triazole compound represented by formula (1): R1 represents an alkyl group, a cycloalkyl group, an alkoxy group, a cycloalkoxy group, an aryl group, an aryloxy group, a monovalent heterocyclic group or a substituted amino group, R2 and R3 each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, a monovalent heterocyclic group or a substituted amino group, and Ring A and Ring B each independently represent an aromatic hydrocarbon ring or an aromatic heterocyclic ring.