Hai cercato: 2,2,2-Trifluoroethyl+methacrylate

Fornitore: TCI

Descrizione: 1,4-Diazabicyclo[2.2.2]octane ≥98.0% (by GC, titration analysis)

Fornitore: Apollo Scientific

Descrizione: Bicyclo[2.2.2]octane-1,4-diyldimethanol

Codice catalogo: (APOSPC512010-1G)

Fornitore: Apollo Scientific

Codice articolo fornitore: PC512010-1G

Codice articolo locale: APOSPC512010-1G

Descrizione: N-[(1S)-1-(3-Bromophenyl)ethyl]-2,2,2-trifluoro-ethanamine hydrochloride

UOM: 1 * 1 g

Promo

Codice catalogo: (APOSPC512008-1G)

Fornitore: Apollo Scientific

Codice articolo fornitore: PC512008-1G

Codice articolo locale: APOSPC512008-1G

Descrizione: N-[(1S)-1-(2-Bromophenyl)ethyl]-2,2,2-trifluoro-ethanamine hydrochloride

UOM: 1 * 1 g

Promo

Fornitore: TCI

Descrizione: Bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride ≥98.0% (by GC, titration analysis), purified by sublimation

Fornitore: Thermo Fisher Scientific

Descrizione: 4-Hydroxymethyl-2,6,7-trioxa-1-phosphabicyclo[2.2.2]octane-1-oxide 98%

Certificati

Fornitore: Apollo Scientific

Descrizione: 1-(5-Bromo-3-chloropyridin-2-yl)-2,2,2-trifluoroethanone

Codice catalogo: (BOSSBS-15484R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A488

Codice articolo locale: BOSSBS-15484R-A488

Descrizione: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15484R-A555)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A555

Codice articolo locale: BOSSBS-15484R-A555

Descrizione: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-15484R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-15484R-A680

Codice articolo locale: BOSSBS-15484R-A680

Descrizione: HIBCH is a 386 amino acid protein belonging to the enoyl-CoA hydratase/isomerase family. Localising to the mitochondria, HIBCH is highly expressed in liver and kidney, with lower levels found in heart, muscle and brain. HIBCH hydrolyses HIBYL-CoA, a saline catabolite, and _-hydroxypropionyl-CoA, an intermediate in the minor pathway involved in the metabolism of proprionate. Existing as two alternatively spliced isoforms, the gene encoding HIBCH maps to human chromosome 2q32.2. Defects to this gene result in HIBCH deficiency (HIBCHD), known alternatively as deficiency of _-hydroxyisobutyryl CoA deacylase or methacrylic aciduria. HIBCHD is characterised by the accumulation of methacrylyl-CoA, a highly reactive compound that undergoes addition reactions with free sulfhydryl groups. Phenotypic symptoms include early deterioration of neurological function, delayed motor skill development and hypotonia.

UOM: 1 * 100 µl

Promo

Fornitore: Apollo Scientific

Descrizione: 2'-Amino-2,2,2-trifluoro-4'-(trifluoromethyl)acetophenone

Fornitore: Apollo Scientific

Descrizione: 1-(3-Bromo-5-fluoropyridin-2-yl)-2,2,2-trifluoroethanone

Codice catalogo: (APOSOR33103-1G)

Fornitore: Apollo Scientific

Codice articolo fornitore: OR33103-1G

Codice articolo locale: APOSOR33103-1G

Descrizione: (2E)-2-[(4-Methoxyphenyl)methylidene]-1-azabicyclo[2.2.2]octan-3-one, tech

UOM: 1 * 1 g

Promo

Fornitore: Apollo Scientific

Descrizione: 6-(2,2,2-Trifluoroethoxy)pyridine-3-thio-carboxamide

Codice catalogo: (APOSPC430332-1G)

Fornitore: Apollo Scientific

Codice articolo fornitore: PC430332-1G

Codice articolo locale: APOSPC430332-1G

Descrizione: 2,2,2-Trifluoro-1-(4-benzoylpiperidin-1-yl)ethanone

UOM: 1 * 1 g

Promo

Codice catalogo: (APOSPC410106-1G)

Fornitore: Apollo Scientific

Codice articolo fornitore: PC410106-1G

Codice articolo locale: APOSPC410106-1G

Descrizione: 2-(2,2,2-Trifluoroethoxy)pyridin-3-amine hydrochloride

UOM: 1 * 1 g

Promo