49633-86-5

Basic information

• Product Name: 2-Propenal, 3-chloro-3-phenyl-, (E)-
• CAS NO: 49633-86-5
• Molecular Formula: C9H7ClO
• Molecular Weight: 166.607
• Mol File: 49633-86-5.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: 2-Propenal, 3-chloro-3-phenyl-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenal, 3-chloro-3-phenyl-, (E)-(49633-86-5)
• EPA Substance Registry System: 2-Propenal, 3-chloro-3-phenyl-, (E)-(49633-86-5)

Safety Data

• Hazardous Substances Data: 49633-86-5(Hazardous Substances Data)

Upstream product

• 2579-22-8 Phenylpropargyl aldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 98-86-2 acetophenone 
• 536-74-3 phenylacetylene 
• 93-61-8 N-methyl-N-phenylformamide 
• 10025-87-3 trichlorophosphate 
• 614-27-7 methyl 3-oxo-3-phenylpropionate 

Downstream Products

• 18819-66-4 (Z)-3-chloro-3-phenyl-2-propenoic acid 
• 62403-17-2 β-chloro-cis-cinnamaldehyde-semicarbazone 
• 92434-89-4 β-chloro-cis-cinnamaldehyde phenylhydrazone 
• 3438-48-0 4-phenylpyrimidine 
• 109507-02-0 (γ-dimethylamino-cinnamylidene)-dimethyl-ammonium; chloride 
• 110422-76-9 (γ-dimethylamino-cinnamylidene)-dimethyl-ammonium; picrate 
• 106472-98-4 β-chloro-cis-cinnamaldehyde-(4-nitro-phenylhydrazone) 
• 69202-27-3 5-phenyl-thiophene-2-carboxylic acid anilide 
• 49571-47-3 (Z)-3-phenyl-3-thiocyanatoacrylaldehyde 
• 119858-08-1 3-phenyl-3-thiocyanatoacrylaldehyde 
• 1075-21-4 5-phenylisothiazole 
• 51000-35-2 Mercaptozimtaldehyd 
• 14597-62-7 5-phenylthiophene-2-carboxylic acid methyl ester 
• 81033-36-5 N-(1-Phenyl-3-phenylimino-1-propenyl)benzolamin 

Relevant articles and documents

Novel benzenesulfonamide-bearing pyrazoles and 1,2,4-thiadiazoles as selective carbonic anhydrase inhibitors

Two series comprising 20 novel benzenesulfonamides bearing thioureido-linked pyrazole 8 and amino-1,2,4-thiadiazole 10 were synthesized and assayed as human carbonic anhydrase (hCA) inhibitors against isoforms I and II as well as the tumor-associated isof

Superacid-promoted synthesis of quinoline derivatives

A series of vinylogous imines have been prepared from anilines and cinnamaldehydes. These substrates react in superacidic media to provide quinolines and related compounds. A mechanism for the conversion is proposed which involves the cyclization of dicationic superelectrophilic intermediates. Aromatization of the quinoline ring is thought to occur by superacid-promoted elimination of benzene.

Thermolysis of N-aryl enaminoimine hydrochloride derivatives: A short and general method for the synthesis of pyranoquinolin-3-one and pyranoacridin-3-one derivatives

A short synthesis of 3H-pyrano[3,2-f]quinolin-3-one, 3H-acenaphtho[1,2-b]pyrano-[3,2-f]quinolin-3-one, and 3H-benzo[h]pyrano[3,2-a]acridin-3-one derivatives are described via thermolysis of suitable enaminoimine hydrochloride derivatives.