21474-92-0

Basic information

• Product Name: ethyl 2-formyl-3-methylbutanoate
• Synonyms: ethyl 2-formyl-3-methylbutanoate
• CAS NO: 21474-92-0
• Molecular Formula: C₈H₁₄O₃
• Molecular Weight: 158.2
• Mol File: 21474-92-0.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ethyl 2-formyl-3-methylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-formyl-3-methylbutanoate(21474-92-0)
• EPA Substance Registry System: ethyl 2-formyl-3-methylbutanoate(21474-92-0)

Safety Data

• Hazardous Substances Data: 21474-92-0(Hazardous Substances Data)

Upstream product

• 609-12-1 ethyl 2-bromoisovalerate 
• 122-51-0 orthoformic acid triethyl ester 
• 117442-74-7 (Z)-1-ethoxy-3-methyl-1-trimethylsiloxy-1-butene 
• 68-12-2 N,N-dimethyl-formamide 
• 108-64-5 Ethyl isovalerate 
• 109-94-4 formic acid ethyl ester 
• 87884-39-7 2-hydroxymethyl-3-methyl-butyric acid ethyl ester 
• 107-31-3 Methyl formate 

Downstream Products

• 127870-28-4 2-[1-[(S)-1-((R)-1-Acetylamino-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylamino]-meth-(E)-ylidene]-3-methyl-butyric acid ethyl ester 
• 127870-34-2 2-[1-((S)-1-Acetylamino-2-phenyl-ethylamino)-meth-(E)-ylidene]-3-methyl-butyric acid ethyl ester 
• 607714-45-4 2-(benzyloxyimino-methyl)-3-methyl-butyric acid ethyl ester 
• 607714-66-9 2-(benzyloxyimino-methyl)-3-methyl-butyric acid 
• 607714-87-4 2-(benzyloxyimino-methyl)-N-(1-dimethylcarbamoyl-2,2-dimethyl-propyl)-3-methyl-butyramide 
• 607715-08-2 (R)-2-(Benzyloxyamino-methyl)-N-((S)-1-dimethylcarbamoyl-2,2-dimethyl-propyl)-3-methyl-butyramide 
• 607715-29-7 (R)-2-[(Benzyloxy-formyl-amino)-methyl]-N-((S)-1-dimethylcarbamoyl-2,2-dimethyl-propyl)-3-methyl-butyramide 
• 90031-34-8 2-Phenethylaminomethyl-isovaleriansaeure-ethylester 
• 127870-30-8 2-{[(R)-1-((S)-1-Acetylamino-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylamino]-methyl}-3-methyl-butyric acid ethyl ester; hydrochloride 
• 101575-56-8 4-isopropyl-3-(4-nitro-benzoyloxy)-pyrrole-2-carboxylic acid ethyl ester 
• 1058157-97-3 (S)-2-(4-cyclohexyl-phenoxymethyl)-6-isopropyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one 

Relevant articles and documents

Lewis base catalyzed asymmetric hydrosilylation of α-substituted β-enamino esters: Facile access to enantioenriched β2-amino esters via dynamic kinetic resolution

A chiral Lewis base organocatalyzed asymmetric hydrosilylation of α-substituted β-enamino esters is presented. The reactions proceeded through dynamic kinetic resolution to afford various enantioenriched β2-amino esters with high yields (up to

SUBSTITUTED PHENOXYMETHYL DIHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

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