2938-48-9

Usage

Chemical Properties

white crystals or crystalline powder

InChI:InChI=1/C7H10O3/c1-7(2)4-3-5(8)10-6(7)9/h3-4H2,1-2H3

Upstream product

• 110054-49-4 α,α-Dimethyl-glutarsaeure-mono-(p-brom-phenyl)-ester 
• 514-78-3 canthaxanthin 
• 681-57-2 2,2-dimethylglutaric acid 

Downstream Products

• 100609-86-7 2,4-dimethyl-N-phenyl-glutaramic acid 
• 13051-32-6 dimethyl 2,2-dimethylglutarate 
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• 82607-68-9 αα-dimethyl-γ-(2,5-dimethylbenzoyl)-n-butyric acid 
• 128684-33-3 4-((R)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-2,2-dimethyl-butyric acid 
• 128684-53-7 Boc-D-Phe-Lys(CO(CH₂)2CMe₂CO₂H)-OMe 
• 61468-98-2 αα-dimethyl-γ-(4-methoxybenzoyl)-n-butyric acid 
• 82607-67-8 αα-dimethyl-γ-(2,4-dimethylbenzoyl)-n-butyric acid 
• 82607-69-0 αα-dimethyl-γ-(4-chlorobenzoyl)-n-butyric acid 
• 82607-65-6 αα-dimethyl-γ-(4-methylbenzoyl)-n-butyric acid 
• 85271-75-6 1-Ethyl 6,6-dimethyl-3-oxo-2-(triphenylphosphonio)-heptanedioate 
• 1679-55-6 γ,γ-dimethyl-δ-valerolactone 
• 4830-05-1 3,3-Dimethyltetrahydro-2H-pyran-2-one 
• 3123-97-5 dihydro-5,5-dimethyl-2(3H)-furanone 

Relevant academic research and scientific papers

VITRIFIED STATE STABILIZING AGENT FOR ANIMAL CELL CRYOPRESERVATION SOLUTION

Provided are a vitrification stabilizer for animal cell cryopreservation fluid, and an animal cell cryopreservation fluid that exhibits superior vitrification capacity due to containing said vitrification stabilizer for animal cell cryopreservation fluid. The vitrification stabilizer for animal cell cryopreservation fluid contains an amphoteric polymer compound selected from the group consisting of: (a) an amphoteric polymer compound obtained by reacting ?-poly-L-lysine with butyl succinic acid anhydride and performing carboxylation; (b) an amphoteric polymer compound obtained by reacting ?-poly-L-lysine with butyl succinic acid anhydride and succinic acid anhydride, and performing carboxylation; and (c) an amphoteric polymer compound obtained by reacting ?-poly-L-lysine with a compound represented by formula (I) and performing carboxylation.

PLANT OR MICROORGANISM-DERIVED CAROTENOID-OXYGEN COPOLYMER COMPOSITIONS, METHODS OF IDENTIFYING, QUANTIFYING AND PRODUCING SAME AND USES THEREOF

The present invention relates to carotenoid-oxygen copolymers, compositions, methods of identifying and quantifying carotenoid-oxygen copolymers in food and related sources, and methods of producing compositions comprising same. In one aspect the method of identifying and quantifying carotenoid-oxygen copolymers comprises an analysis of a low molecular weight marker compound in said sources. In another aspect the present invention provides a method of preparing compositions comprising said carotenoid-oxygen copolymers and/or enhancing levels of said copolymers in food sources in a sufficient and practically useful concentration to have beneficial effects in animals and humans, including beneficial immunological and health effects.

Regioselective photochemical rearrangement of N-mesyloxylactams

N-Mesyloxylactams can undergo ring contraction either by C-3 (usually observed) or C-5 migration. C-5 migration can occur when the C-3 migration product possesses ring strain, but it does not usually compete with C-3 migration. The greater preference for C-3 migration is due to the carbonyl oxygen atom, which greatly stabilizes the intermediate. Studies of the photochemical rearrangement of N-mesyloxylactams showed that the lone pair of the carbonyl oxygen atom, and not the degree of the substitution atthe migrating carbon atoms, is the governing factor in the regioselectivity of the reaction. Copyright

Synthesis of Small-Medium Ring Thioanhydrides

Reaction of five-membered ring anhydrides with sodium sulfide has previously been employed for synthesis of the corresponding thioanhydrides in low yields.Re-examination of the stoichiometry reveals reaction of cyclic anhydride with sodium sulfide (2:1 respectively), affords the thioanhydride accompanied by the corresponding dicarboxylate in a 1:1 molar ratio.The mechanistic pathway for this reaction has also been elucidated.Optimization of reaction conditions has resulted in the synthesis of a variety of four to seven-membered ring thioanhydride in yields approaching theoretical.