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Generally, 2-10 mol% of this catalyst is used along with borane-tetrahydrofuran (THF), borane-dimethylsulfide, borane-N,N-diethylaniline, or diborane as the borane source. Enantioselective reduction using chiral oxazaborolidine catalysts has been used in the synthesis of commercial drugs such as ezetimibe and aprepitant .
Chemical formula Synonyms CAS number C 10 H 16 N 2 O 8: Ethylenediaminetetraacetic acid (EDTA): 6381–92–6 C 12 H 22 O 11: sucrose: 57–50–1 C 18 H 29 O 3 S: sodium dodecyl benzenesulfonate: 2155–30–0
C 10 H 12 N 2: tryptamine: 61-54-1 C 10 H 12 O: anethole: C 10 H 12 O: estragole: C 10 H 12 O 2: hinokitiol: C 10 H 12 O 2: eugenol: C 10 H 12 O 2: isoeugenol: C 10 H 12 O 2: pseudoisoeugenol: C 10 H 12 O 3: coniferyl alcohol: C 10 H 13 N 5 O 4: adenosine: 58-61-7 C 10 H 14 ClNS N-tert-Butylbenzenesulfinimidoyl chloride: 49591-20-0 C 10 H 14 Cl ...
Dodecanedioic acid (DDDA) is a dicarboxylic acid with the formula (CH 2) 10 (CO 2 H) 2. A white solid, the compound finds a variety of applications ranging from polymers to materials. A white solid, the compound finds a variety of applications ranging from polymers to materials.
Cocamide MEA, or cocamide monoethanolamine, is a solid, off-white to tan compound, often sold in flaked form.The solid melts to yield a pale yellow viscous clear liquid. It is a mixture of fatty acid amides which is produced from the fatty acids in coconut oil when reacted with ethanolamin
Tris(8-hydroxyquinolinato)aluminium is the chemical compound with the formula Al(C 9 H 6 NO) 3. Widely abbreviated Alq 3 , it is a coordination complex wherein aluminium is bonded in a bidentate manner to the conjugate base of three 8-hydroxyquinoline ligands .
Dodecanal, also known as lauraldehyde or dodecyl aldehyde, is an organic compound with the chemical formula CH 3 (CH 2) 10 CHO. This colourless liquid is a component of many fragrances. It occurs naturally in citrus oils, but commercial samples are usually produced from dodecanol by dehydrogenation. [2]
Another route to specific di- or triglycerides involves converting the solketal to glycidol (2,3-epoxy-1-propanol) and esterifying this with one fatty acid before opening the epoxy by heating in the presence of a second fatty acid and a catalyst. This second fatty acid is put on the third carbon atom, and then a third fatty acid can be added to ...