57204-90-7

Basic information

• Product Name: 4-Heptanone, 3-(phenylseleno)-
• CAS NO: 57204-90-7
• Molecular Formula: C13H18OSe
• Molecular Weight: 269.245
• Mol File: 57204-90-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-Heptanone, 3-(phenylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Heptanone, 3-(phenylseleno)-(57204-90-7)
• EPA Substance Registry System: 4-Heptanone, 3-(phenylseleno)-(57204-90-7)

Safety Data

• Hazardous Substances Data: 57204-90-7(Hazardous Substances Data)

Upstream product

• 71098-88-9 N-phenylselanylphthalimide 
• 123-19-3 4-heptanone 
• 34837-55-3 Phenylselenyl bromide 
• 72551-28-1 (Z)-(1-propyl)-1-butenyl trimethylsilyl ether 
• 82737-08-4 N-(phenylselanyl)morpholine 
• 1666-13-3 diphenyl diselenide 
• 5707-04-0 Phenylselenyl chloride 

Downstream Products

• 56253-60-2 trimethyl-phenylselanylmethyl-silane 
• 84993-31-7 ((E)-2-Propyl-pent-2-enylselanyl)-benzene 

Relevant articles and documents

ORGANOCATALYSTS AND METHODS OF USE IN CHEMICAL SYNTHESIS

The present invention pertains generally to compositions comprising organocatalysts that facilitate stereo-selective reactions and the method of their synthesis and use. Particularly, the invention relates to metal-free organocatalysts for facilitation of stereo--selective reactions, and the method of their synthesis and use. These compounds have the structure of the Formulas (I) and (II). Where X is independently selected from CH2, N-Ra, O, S or C=O; Y is CH2, N-Ra, O, S or C=O, with the proviso that at least one of X or Y is CH2, and preferably both of X and Y are CH2; Ra is H, an optionally substituted C1-C12 alkyl, preferably an optionally substituted C1-C6alkyl including a C3-C6 cyclic alkyl group, or an optionally substituted aryl group, preferably an optionally substituted phenyl group; Rb is H, an optionally substituted C1-C12 alkyl, preferably an optionally substituted C1-C6 acyclic or a a C3-C6 cyclic alkyl group, CHO, N(Me)O, CO(S)Ra or the group of Formula (III). Where Rc and Rd are each independently H, F, C1, an optionally substituted C1-C20 alkyl, preferably an optionally substituted C1-C12 alkyl, more preferably a C1-C6 alkyl, and an optionally substituted aryl group, or together Rc and Rd form an optionally substituted carbocyclic or optionally substituted heterocyclic ring; R1 is OH, OR, NR'R", NHC(=O)R, NHSO2R; R2 is H, F, C1, an optionally substituted C1-C20 alkyl, preferably an optionally substituted C1-C6 alkyl, an optionally substituted aryl group or a =O group (which establishes a carbonyl group with the carbon to which =O is attached; R3 is H, OH, F, C1, Br, I, Cl, an optionally substituted C1-C20 alkyl, alkenyl or alkynyl ("hydrocarbyl") group, preferably an optionally substituted C1-C6 alkyl, or an optionally substituted aryl, such that the carbon to which R3 is attached has an R or S configuration; R is H, an optionally substituted C1-C20 alkyl, preferably an optionally substituted C1-C6 alkyl, or an optionally substituted aryl group, R' and R" are each independently H, an optionally substituted C1-C20 alkyl group, preferably an optionally substituted C1-C6 alkyl, or an optionally substituted aryl group; or together R' and R" form an optionally substituted heterocyclic, preferably a 4 to 7 membered optionally substituted heterocyclic group or an optionally substituted heteroaryl ring with the nitrogen to which R' and R" are attached; and wherein said compound is free from a metal catalyst.

Preparations de composes α-arylselenocarbonyles a l'aide de morpholinoareneselenenamides

The reactivity of the morpholinoareneselenenamides 1 which are readily prepared from various diaryldiselenides, is investigated.The selenenamides 1 are good α-selenenylating agents for aliphatic aldehydes, α-ketoesters and conjugated enals yielding the α-