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5-Bromo-4-chloro-2-methoxybenzonitrile
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5-Bromo-4-chloro-2-methoxybenzonitrile
Artikel-Nr:
(COWI001.1135)
Lieferant:
COWIE
Hersteller-Artikelnummer::
001.1135
Lokale Artikelnummer::
COWI001.1135
Beschreibung:
Double cross-head has a greater turbulance when compared to single cross-head.
VE:
1 * 1 ST
Artikel-Nr:
(BLDPBD200240-250MG)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD200240-250MG
Lokale Artikelnummer::
BLDPBD200240-250MG
Beschreibung:
5-(Chloromethyl)-3-(4-methoxyphenyl)isoxazole 95%
VE:
1 * 250 mg
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-Fluor-5-(trifluormethyl)phenylacetonitril 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Methyl 1,6-dihydro-1-(4-fluorophenyl)-6-oxopyridine-3-carboxylate 97%
Artikel-Nr:
(75633-2ML)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
75633-2ML
Lokale Artikelnummer::
SIAM75633-2ML
Beschreibung:
Osmium tetroxide solution has been used as a fixative in electron microscopy.
VE:
1 * 2 mL
Artikel-Nr:
(9753.1000)
Lieferant:
Avantor
Lokale Artikelnummer::
BAKR9753.1000
Beschreibung:
N,N-Dimethylformamid ≥99,9%, BAKER ANALYZED® für die Headspace-Gaschromatographie, J.T.Baker®
VE:
1 * 1 L
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Fluor-o-toluonitril
Artikel-Nr:
(USBI037604-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
037604-BIOTIN
Lokale Artikelnummer::
USBI037604-BIOTIN
Beschreibung:
Anti-KRT12 Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 µl
Artikel-Nr:
(BOSSBS-11945R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11945R-A488
Lokale Artikelnummer::
BOSSBS-11945R-A488
Beschreibung:
Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf52 gene product has been provisionally designated C12orf52 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9947R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9947R-A680
Lokale Artikelnummer::
BOSSBS-9947R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf40 gene product has been provisionally designated C12orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9945R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9945R-A680
Lokale Artikelnummer::
BOSSBS-9945R-A680
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf24 gene product has been provisionally designated C12orf24 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9953R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9953R-A750
Lokale Artikelnummer::
BOSSBS-9953R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The C12orf61 gene product has been provisionally designated C12orf61 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9955R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9955R-A750
Lokale Artikelnummer::
BOSSBS-9955R-A750
Beschreibung:
Encoding over 1100 genes within 132 million bases, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The LOC387856 gene product has been provisionally designated LOC387856 pending further characterisation.
VE:
1 * 100 µl
Lieferant:
SGE Analytical Science
Beschreibung:
Einzigartige Hochtemperatur-Phase, geeignet für simulierte Destillation und andere Mineralöl-Anwendungen.
Artikel-Nr:
(H57213.03)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
H57213.03
Lokale Artikelnummer::
ALFAH57213.03
Beschreibung:
(S)-1-Boc-4-oxo-piperidine-2-carboxylic acid methyl ester 95%
VE:
1 * 1 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
1,4-Bis(bromodifluoromethyl)benzene
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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