84736-00-5

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 1611-78-5 1,3-bis-dimethylaminotrimethinium perchlorate 
• 118000-07-0 (Z)-2-[(4-Chloro-phenyl)-morpholin-4-yl-methyl]-3-hydroxy-propenal 

Downstream Products

• 118000-07-0 (Z)-2-[(4-Chloro-phenyl)-morpholin-4-yl-methyl]-3-hydroxy-propenal 
• 118036-03-6 C₁₆H₁₉ClN₂O₂ 
• 116733-12-1 (Z)-2-Acetyl-3-(4-chloro-phenyl)-4-formyl-5-hydroxy-pent-4-enoic acid ethyl ester 
• 104409-68-9 4-(4-Chloro-phenyl)-2-dimethylamino-4H-[1,3]oxazine-5-carbaldehyde 
• 88382-34-7 3-(4-Chloro-phenyl)-4-formyl-3H-furan-2,2-dicarboxylic acid diethyl ester 
• 118000-10-5 (Z)-2-[(4-Chloro-phenyl)-dimethylamino-methyl]-3-hydroxy-propenal 
• 84735-94-4 4-(4-Chloro-phenyl)-6-ethoxy-5,6-dihydro-4H-pyran-3-carbaldehyde 
• 104449-83-4 2-formyl-3-anilino-3-(4-chlorophenyl)acrylic acid 
• 119021-94-2 3-(4-Chloro-phenyl)-2,2,2-trimethoxy-2,3-dihydro-2λ⁵-[1,2]oxaphosphole-4-carbaldehyde 
• 119021-90-8 [(E)-1-(4-Chloro-phenyl)-2-formyl-3-hydroxy-allyl]-phosphonic acid dimethyl ester 
• 119021-85-1 [(E)-1-(4-Chloro-phenyl)-2-formyl-3-methoxy-allyl]-phosphonic acid dimethyl ester 
• 118000-17-2 (Z)-2-(4-Chloro-phenyl)-3-formyl-4-methoxy-but-3-enenitrile 
• 116733-20-1 4-(4-Chloro-phenyl)-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbaldehyde 
• 116733-29-0 2-Amino-4-(4-chloro-phenyl)-5-formyl-4H-pyran-3-carboxylic acid methyl ester 

Relevant academic research and scientific papers

REACTION OF ARYLMETHYLENEMALONALDEHYDES WITH SOME NUCLEOPHILES

Reaction of arylmethylenemalonaldehydes with tributylphosphine and tertiary amines affords compounds of dipolar structure whereas reaction with primary and secondary amines leads to 1,4-addition products.Salts of nucleophilic inorganic anions add to arylm

SYNTHESIS OF BENZYLIDENEMALONALDEHYDES

A general two step synthesis of benzylidenemalonaldehydes (V), based on condensation of substituted benzaldehydes with 1,3-bis(dimethylamino)trimethinium perchlorate, is described.The course of this reaction, character of the intermediate and spectral cha

ARYLMETHYLENEMALONALDEHYDES AND THEIR HETEROCYCLIC ANALOGUES: A NOVEL GROUP OF ORGANIC LEWIS ACIDS

The first general synthesis of arylmethylenemalonaldehydes and their heterocyclic analogues has been developed; some physico-chemical properties and reactions of these compounds are briefly mentioned.