16979-50-3

Basic information

• Product Name: 3-benzylsulfanyl-propionaldehyde
• Synonyms: 3-benzylsulfanyl-propionaldehyde
• CAS NO: 16979-50-3
• Molecular Weight: 180.271
• Mol File: 16979-50-3.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 3-benzylsulfanyl-propionaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-benzylsulfanyl-propionaldehyde(16979-50-3)
• EPA Substance Registry System: 3-benzylsulfanyl-propionaldehyde(16979-50-3)

Safety Data

• Hazardous Substances Data: 16979-50-3(Hazardous Substances Data)

Upstream product

• 75908-55-3 3-(benzylthio)-1,2-benzisothiazole 1,1-dioxide 
• 107-02-8 acrolein 
• 5601-23-0 3-(benzylthio)propanenitrile 
• 100-39-0 benzyl bromide 
• 100-53-8 phenylmethanethiol 
• 32380-88-4 3-benzylthiopropanal diethyl acetal 
• 32362-99-5 benzylthioacetate 

Downstream Products

• 100612-33-7 5-benzylsulfanyl-pent-2ξ-enoic acid methyl ester 
• 86116-20-3 3-benzylsulfanyl-propionaldehyde-(2,4-dinitro-phenylhydrazone) 
• 122538-55-0 5-benzylsulfanyl-pent-2-enoic acid ethyl ester 
• 77275-31-1 diphenyl [(RS)-1-(3-phenylthioureido)-3-(benzylsulfanyl)propyl]phosphonate 
• 77275-38-8 [(RS)-1-amino-3-(benzylsulfanyl)propyl]phosphonic acid 
• 172295-18-0 5-(benzylthio)-3-hydroxy-1-pentene 
• 732229-67-3 (S)-2-(3-Benzylsulfanyl-propylamino)-4-methyl-pentanoic acid 
• 192123-80-1 (2S,3S)-2-(3-Benzylsulfanyl-propylamino)-3-methyl-pentanoic acid 
• 192123-54-9 N^α-<3-(Benzylthio)propyl>phenylalanine 
• 945410-09-3 ethyl (E)-5-benzylsulfanylpent-2-enoate 
• 945410-12-8 C₂₁H₂₆O₃S₂ 
• 945410-10-6 C₁₉H₂₄OS₂ 
• 945410-11-7 C₂₅H₃₄O₃S₂ 
• 122538-56-1 3,5-bis-benzylsulfanyl-pentanoic acid ethyl ester 

Relevant articles and documents

Biomimetic alloxan-catalyzed intramolecular redox reaction with O2: One-pot atom-economic synthesis of sulfinyl-functionalized benzimidazoles

Given the necessity of sacrificial reductants in various biomimetic aerobic oxygenations, alloxan-catalyzed aerobic redox system for one-pot atom-economic synthesis of sulfinyl-functionalized benzimidazoles was developed by ingeniously binding both the substrate sulfide and sacrificial reductant. This mild and transition-metal-free protocol undergoes two oxidations without additional sacrificial reagents, except for the environmentally benign molecular oxygen.

Enantioselective Iridium-Catalyzed Allylation of Nitroalkanes: Entry to β-Stereogenic α-Quaternary Primary Amines

The first systematic study of simple nitronate nucleophiles in iridium-catalyzed allylic alkylation is described. Using a tol-BINAP-modified π-allyliridiumC,O-benzoate catalyst, α,α-disubstituted nitronates substitute racemic branched alkyl-substituted al

1,2-DITHIOLANE AND DITHIOL COMPOUNDS USEFUL IN TREATING MUTANT EGFR-MEDIATED DISEASES AND CONDITIONS

Compositions of the invention comprise 1,2-dithiolane, dithiol and related compounds useful as therapeutic agents for the treatment and prevention of diseases and conditions associated with aberrant EGFR activity.