4094-64-8

Basic information

• Product Name: 3-methyl-3-phenyl-butyryl chloride
• Synonyms: 3-methyl-3-phenyl-butyryl chloride
• CAS NO: 4094-64-8
• Molecular Weight: 196.677
• Mol File: 4094-64-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 3-methyl-3-phenyl-butyryl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-3-phenyl-butyryl chloride(4094-64-8)
• EPA Substance Registry System: 3-methyl-3-phenyl-butyryl chloride(4094-64-8)

Safety Data

• Hazardous Substances Data: 4094-64-8(Hazardous Substances Data)

Upstream product

• 6325-41-3 3-methyl-3-phenylbutanal 
• 1010-48-6 3-methyl-3-phenylbutanoic acid 
• 56-23-5 tetrachloromethane 
• 94-36-0 dibenzoyl peroxide 
• 71-43-2 benzene 
• 79-37-8 oxalyl dichloride 
• 7403-42-1 4-Methyl-4-phenyl-2-pentanone 
• 541-47-9 3-Methylbutenoic acid 

Downstream Products

• 26465-81-6 3,3-dimethylindan-1-one 
• 132105-23-8 2,2,5-trimethyl-5-phenyl-hexan-3-ol 
• 3990-83-8 β-Phenyl-perisovaleriansaeure-tert-butylester 
• 62698-29-7 Benzoyl-β-phenylisovalerylperoxid 
• 93163-09-8 2.3.6-Trimethyl-6-phenyl-hepten-⁽¹⁾-on-⁽⁴⁾ 
• 93142-71-3 1-Butyl-3-(β-phenyl-isovaleryl)-harnstoff 
• 62698-31-1 3-Methyl-3-phenyl-butyric acid 1,1-dimethyl-2-phenyl-ethyl ester 
• 62698-30-0 3-Methyl-3-phenyl-butyric acid 2-methyl-2-phenyl-propyl ester 
• 57260-21-6 1-(3-methyl-3-phenyl-butyryl)-4-(4-oxo-5-phenyl-4,5-dihydro-oxazol-2-yl)-piperazine 
• 51380-79-1 β-phenylisovaleryl p-nitrobenzoyl peroxide 
• 62726-47-0 β-phenylisovaleryl peroxide 
• 138453-06-2 p-methoxy-3,3-dimethyl-3-phenylpropiophenone 
• 180737-12-6 1-diazo-4-methyl-4-phenylpentan-2-one 
• 768-49-0 (2-methyl-1-propenyl)-benzene 

Relevant articles and documents

Copper-Mediated, Heterogeneous, Enantioselective Intramolecular Buchner Reactions of α-Diazoketones Using Continuous Flow Processing

Enantioselective intramolecular Buchner reactions of α-diazoketones can be effected using heterogeneous copper-bis(oxazoline) catalysts in batch or using continuous flow processing in up to 83% ee. The catalyst can be reused up to 7 times without loss of activity. For α-diazoketones 3 and 4, the enantioselection achieved in flow with the immobilized catalyst was comparable with the standard homogeneous catalyzed process.

Preparation of α-amino acids by oxidative oxazoline-oxazinone rearrangement-hydrogenation (OOOH). Scope and limitations

The range and scope of the oxidative oxazoline-oxazinone rearrangement-hydrogenation sequence (OOOH)-a short, direct asymmetric synthesis of α-amino acids from carboxylic acids-was explored. The highest yet reported diastereoselectivity for hydrogenation of the oxazinone C=N bond (d.r.=>80:1) is disclosed and rationalized with the aid of ab initio molecular calculations.

Pyrazolopyrimidines as therapeutic agents

The present invention is directed to pyrazolopyrimidine derivatives of formula (I) wherein the substituents are defined herein, which are useful as kinase inhibitors and as such are useful for affecting angiogenesis and diseases and conditions associated with angiogenesis.