A banana protective device for storing and transporting a banana carefully.
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| Number | Title | Issue Date |
| 8088954 | Preparation of a saturated aldehyde The invention relates to a compound according to Formula (IX) and salts thereof, wherein R1, R2 and R5 are each independently selected from H and hydrocarbon moieties, which hydrocarbon moieties optionally comprise one or more hetero... | 01/03/2012 |
| 6909019 | Process for preparing aldehydes A process is disclosed for preparing aldehydes by isomerization of the corresponding unsaturated primary alcohols using a transition metal catalyst system, in an alcoholic solvent and in the presence of an acid. An aldehyde forms by isomerizing an unsaturated primar... | 06/21/2005 |
| 5770775 | Method for preparing 3,3-dimethylbutyraldehyde A method is disclosed for preparing 3,3-dimethylbutyraldehyde by isomerization of 3,3-dimethylepoxybutane with a basic lithium salt which in turn may be prepared by oxidation of dimethylbutane. The method provides an economical means of preparing 3,3-dime... | 06/23/1998 |
| 5502257 | Process for the production of cyclopropanecarboxaldehyde Disclosed is a process for the preparation of cyclopropanecarboxaldehyde by the thermal isomerization of 2,3-dihydrofuran under superatmospheric pressure, e.g., at a temperature of about 300° to 600° C. and a pressure of about 3 to 345 bars absolute.... | 03/26/1996 |
| 5481044 | Process for the preparation of -alkyl substituted aldehydes -alkyl aldehydes having 8 to 17 carbon atoms are obtained from terminal olefins containing one less carbon atom. The olefins are first isomerized in the presence of iron carbonyl and then, without separating out the iron compound, hydroformylated i... | 01/02/1996 |
| 5430194 | Process for improving enantiomeric purity of aldehydes The present invention relates to a process for producing an optically active aldehyde (first aldehyde) containing a reduced amount of the corresponding enantiomeric aldehyde (second aldehyde) which process comprises: (1) providing an initial solution cont... | 07/04/1995 |
| 5312995 | Process for isomerizing epoxides to aldehydes A process for isomerizing epoxides to aldehydes is disclosed. The process uses a metal-exchanged zeolite catalyst wherein the zeolite contains an alkali metal and one or more second exchangeable metals from Group IIA, IB, IIB, or IIIB. The catalysts are e... | 05/17/1994 |
| 5245041 | Preparation of heterocyclic-cyclohexanedione derivatives A process for the preparation of cyclohexanedione derivatives of the general formula I ##STR1## where R1 is C2 -C8 -alkyl, C2 -C8 -alkenyl, C3 -C12 -cycloalkyl, C5 | 09/14/1993 |
| 5225602 | Phenylacetaldehydes and the preparation of phenylacetaldehydes Phenylacetaldehydes of the structure (I) ##STR1## where the substituents X are 2,4-dichloro, difluoro, trifluoro, tetrafluoro, p-trifluoromethyl, 2-methyl-4-fluoro, haloalkoxy or haloalkylthio radicals or are adjacent Cl, F, CF3, alkyl, al... | 07/06/1993 |
| 5012005 | Conversion of 1,3-dioxanes to 4-oxaaldehydes 4-oxaaldehydes of the formula ##STR1## are prepared by catalytic isomerization of 1,3-dioxanes by a process in which a 1,3-dioxane of the formula ##STR2## where R1, R2, R4 and R5 are identical or diffe... | 04/30/1991 |
| 4996365 | Preparation of alkyl-substituted cinnamaldehydes Alkyl-substituted cinnamaldehydes of the formula I ##STR1## where one or more of R1 , R2 and R3 is alkyl of from 1 to 8 carbon atoms, preferably of from 1 to 4 carbon atoms, and non-alkyl R1, R2 ... | 02/26/1991 |
| 4980511 | Preparation of aldehydes and/or ketones BU conversion of epoxides Aldehydes and ketones are prepared from epoxides of the formula ##STR1## where R1 and R2 are each alkyl, alkenyl, aryl, alkoxy or aralkyl and R3 has the same meanings or is hydrogen, by a catalytic rearrangement react... | 12/25/1990 |
| 4929765 | Preparation of phenylacetaldehydes Phenylacetaldehydes of the general formula I ##STR1## where R1 to R5 are each independently of the others hydrogen, alkyl, alkoxy, halogen, haloalkyl, haloalkoxy or haloalkylthio, by catalytic rearrangement in the presence of a ... | 05/29/1990 |
| 4749814 | Process for the preparation of ethylenic carbonyl compounds Ethylenic carbonyl compounds of formula ##STR1## are made by the isomerization of acetylenic alcohols of formula ##STR2## in the presence of a catalyst consisting of a titanium derivative, a copper or silver derivative, and, if required, an acid... | 06/07/1988 |
| 4749815 | Process for the manufacture of p-tert-butyl-alpha-methyl-hydrocinnamaldehyde A process for the manufacture of p-tert-butyl--methylhydrocinnamaldehyde which comprises the catalytic rearrangement of p-tert-butylbenzyl propenyl ether is provided.... | 06/07/1988 |
| 4709097 | Conversion of 1,3-dioxanes to 4-oxa-aldehydes 4-oxa-aldehydes are prepared by catalytic isomerization of a 1,3-dioxane using an acidic zeolite catalyst.... | 11/24/1987 |
| 4670607 | Method for producing 2-(substituted aryl) propionaldehyde A 2-(substituted aryl)propionaldehyde of the formula, ##STR1## (wherein Ar denotes ##STR2## is produced in high yield by reacting a methyl (substituted aryl) ketone of the formula ##STR3## with phenyldimethylsulfonium methylsulfate of ... | 06/02/1987 |
| 4650908 | Production of arylacetaldehydes This invention relates to the isomerization of monoaryl-ethylene oxide in the presence of water over a silica gel catalyst. Reaction temperatures are relatively low, i.e., 160° C. to about 180° C.... | 03/17/1987 |
| 4621150 | Catalyst and method for isomerization A catalyst for isomerization consisting essentially of a salt or complex salt represented by the formula: where M is a metal of Group IB, IIA, IIB or VIII of the periodic table, L is a ligand, Y is a conjugated base of a Bronsted acid, m is 0, 1, 2, 3 or ... | 11/04/1986 |
| 4593130 | Synthesis of 10-hydroxymethyl-9-anthraldehyde This disclosure describes the catalyzed rearrangement of trans-dispiro (oxirane-2,9-(10'H)-anthracene)-10',2"-oxirane to 10-hydroxymethyl-9-anthraldehyde.... | 06/03/1986 |
| 4495371 | Process for isomerizing styrene oxide or homologues to ଲ-phenylaldehydes A process for isomerizing styrene or homologues to ଲ-phenylaldehydes, consisting of conducting the isomerization reaction in the presence of a catalyst constituted by synthetic zeolites containing titanium, of formula where x lies between 0.0001 and 0.04... | 01/22/1985 |
| 4324921 | Process for the manufacture of ethers of hydroxy-pivalaldehyde Ethers of the hydroxypivalaldehyde RCH2 OCH2 C(CH3)2 CHO are prepared by a catalytic isomerization of 5,5-dimethyl-1,3-dioxans at 250° to 500° C. The catalyst is obtained by way of calcination from silicon dio... | 04/13/1982 |
| 4310709 | Manufacture of but-2-en-1-ol compounds by isomerizing the corresponding but-3-en-1-ol compounds The process for the manufacture of but-2-en-1-ol compounds by isomerizing but-3-en-1-ol compounds in the presence of a palladium catalyst and of hydrogen is improved by modifying the palladium catalyst with selenium or tellurium. The but-2-en-1-ols manufa... | 01/12/1982 |
| 4145366 | Process for isomerizing one of the geometric isomers of an ,ଲ-unsaturated aldehyde to its corresponding other geometric isomer Process for preparing a trans-,ଲ-unsaturated aldehyde or a cis-,ଲ-unsaturated aldehyde at high conversions and selectivities, which comprises isomerizing a cis-,ଲ-unsaturated aldehyde to its corresponding trans-... | 03/20/1979 |
| 4124643 | Preparation of 3-fluorosalicylaldehyde 3-Fluorosalicylaldehyde may be prepared in a more economical manner by alkylating o-fluorophenol with an allyl halide such as allyl chloride, thereafter rearranging the resultant o-fluorophenyl allyl ether to form allyl-o-fluorophenol. The latter compound... | 11/07/1978 |
| 4028278 | Cycloaliphatic unsaturated ketones as fragrance modifying agents New cycloaliphatic unsaturated ketones and their use as perfuming and odor-modifying agents in the manufacture of perfumes and perfumed products, and as flavoring and taste-modifying agents in the preparation of foodstuffs in general and imitation flavors... | 06/07/1977 |
| 3976684 | 1-Succinoyl-2,4-disubstituted-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-ph enanthrenes and compositions and methods for treating lipodemia 1-succinoyl-2,4-disubstituted-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-phenanthre nes, e.g., 1-succinoyl-2,4-dimethoxy-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-phenanthrene are prepared by treating a corresponding 2,4-dimethoxy-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-... | 08/24/1976 |