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5-Acetyl-8-(phenylmethoxy)quinoline
5-Acetyl-8-(phenylmethoxy)quinoline
United States Biological

Used in the preparation of phenylethanolamine derivatives as b2 adrenoreceptor agonists. Form: Pale Yellow Solid Solubility: Chloroform

8-Benzyloxy-5-(2-bromoacetyl)-2(1H)-quinolinone
8-Benzyloxy-5-(2-bromoacetyl)-2(1H)-quinolinone
United States Biological

Used in the preparation of phenylethanolamine derivatives as b2 adrenoreceptor agonists. Form: Off-white Solid Solubility: Chloroform

8-Benzyloxy-5-((R)-2-bromo-1-hydroxyethyl)-1H-quinolinone
8-Benzyloxy-5-((R)-2-bromo-1-hydroxyethyl)-1H-quinolinone
United States Biological

Used in the preparation of phenylethanolamine derivatives as b2 adrenoreceptor agonists. Form: Light Brown Solid Solubility: Methanol

5-Acetyl-8-(phenylmethoxy)-2-quinoline N-Oxide
5-Acetyl-8-(phenylmethoxy)-2-quinoline N-Oxide
United States Biological

Used in the preparation of phenylethanolamine derivatives as b2 adrenoreceptor agonists. Form: Light Brown Solid Solubility: Methanol

2,5-Dimethoxy-4-methyl-benzaldehyde
2,5-Dimethoxy-4-methyl-benzaldehyde
United States Biological

Used in the preparation of phenylamine derivative as potential psychotomimetics. Form: Yellow Solid Solubility: Dichloromethane, Methanol

1-[(2-Chlorophenyl)thio]-2-propanone
1-[(2-Chlorophenyl)thio]-2-propanone
United States Biological

Used in the preparation of pharmacologically active benzo[b]thiophene derivatives. Form: Light Yellow Oil Solubility: Chloroform, Dichloromethane, Ethyl...

(1S,3aR,6aS)-Hexahydro-cyclopenta[c]pyrrole-1,2(1H)-dicarboxylic Acid 2-(tert-Butyl) Ester
(1S,3aR,6aS)-Hexahydro-cyclopenta[c]pyrrole-1,2(1H)-dicarboxylic Acid 2-(tert-Butyl) Ester
United States Biological

Used in the preparation of peptidomimetic protease inhibitors. Form: White Solid

(1S,3aR,6aS)-Hexahydro-cyclopenta[c]pyrrole-1,2(1H)-dicarboxylic Acid Bis(tert-butyl) Ester
(1S,3aR,6aS)-Hexahydro-cyclopenta[c]pyrrole-1,2(1H)-dicarboxylic Acid Bis(tert-butyl) Ester
United States Biological

Used in the preparation of peptidomimetic protease inhibitors. Form: Oil Solubility: Dichloromethane

1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde
1,3-Di-O-tert-butyldimethylsilyl Paricalcitol 18-Aldehyde
United States Biological

Used in the preparation of Paricalcitol. Form: White Sticky Solid Solubility: Dichloromethane, Ethyl Acetate, Methanol

N,N-Dimethyl-L-histidine-d6 Methyl Ester Dihydrochloride
N,N-Dimethyl-L-histidine-d6 Methyl Ester Dihydrochloride
United States Biological

Used in the preparation of optically pure labeled L-(+)-Ergothioneine. Form: Light Green Oil Solubility: Methanol, Water

L-Histidine Methyl Ester Dihydrochloride
L-Histidine Methyl Ester Dihydrochloride
United States Biological

Used in the preparation of optically pure L-(+)-Ergothioneine. Form: White to Off-White Solid Melting Point: >190 degrees C (dec.) Solubility: DMSO,...

3',5'-O-[Tetrakis(1-methylethyl)-1,3-disiloxanediyl]guanosine-13C,15N2
3',5'-O-[Tetrakis(1-methylethyl)-1,3-disiloxanediyl]guanosine-13C,15N2
United States Biological

Used in the preparation of nucleotide analogs. Form: White Solid Solubility: Methanol

3',5'-O-[Tetrakis(1-methylethyl)-1,3-disiloxanediyl]guanosine
3',5'-O-[Tetrakis(1-methylethyl)-1,3-disiloxanediyl]guanosine
United States Biological

Used in the preparation of nucleotide analogs. Form: White Solid Solubility: Methanol

(1R,2R,3S,5S)-2-Hydroxy-6-oxabicyclo[3.1.0]hexane-3-methanol
(1R,2R,3S,5S)-2-Hydroxy-6-oxabicyclo[3.1.0]hexane-3-methanol
United States Biological

Used in the preparation of nucleoside derivatives as inhibitors of E1 activating enzymes. Form: Colorless Oil Solubility: Chloroform, Ethyl Acetate, Methanol

(1aS,1bR,5aS,6aS)-Hexahydro-3-(4-methoxyphenyl)-oxireno[4,5]cyclopenta[1,2-d][1,3]dioxin
(1aS,1bR,5aS,6aS)-Hexahydro-3-(4-methoxyphenyl)-oxireno[4,5]cyclopenta[1,2-d][1,3]dioxin
United States Biological

Used in the preparation of nucleoside derivatives as antitumor agents, E1 activating enzymes and MLN4924, an inhibitor of NEDD8-activating enzyme. Form:...

N-[(1S)-2,3-Dihydro-1H-inden-1-yl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
N-[(1S)-2,3-Dihydro-1H-inden-1-yl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
United States Biological

Used in the preparation of nucleoside derivatives as antitumor agents, E1 activating enzymes and MLN4924, an inhibitor of NEDD8-activating enzyme. Form:...

(4aS,6R,7S,7aR)-6-[4-[[(1S)-2,3-Dihydro-1H-inden-1-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl]hexahydro-2-(4-methoxyphenyl)-cyclopenta-1,3-dioxin-7-ol
(4aS,6R,7S,7aR)-6-[4-[[(1S)-2,3-Dihydro-1H-inden-1-yl]amino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl]hexahydro-2-(4-methoxyphenyl)-cyclopenta-1,3-dioxin-7-ol
United States Biological

Used in the preparation of nucleoside derivatives as antitumor agents, E1 activating enzymes and MLN4924, an inhibitor of NEDD8-activating enzyme. Form:...

9-[(4,4,5,5,5-Pentafluoropentyl)thio]nonanol
9-[(4,4,5,5,5-Pentafluoropentyl)thio]nonanol
United States Biological

Used in the preparation of N-phenylcarboxamide derivatives as antitumor agents. Form: Yellow Semi-solid Solubility: Dichloromethane, Ethyl Acetate, Hexane,...

3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolylcarboxylic Acid Ethyl Ester
3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolylcarboxylic Acid Ethyl Ester
United States Biological

Used in the preparation of novel isoxazole carboxamides as growth hormones. Form: Off-white Solid Solubility: Chloroform, Dichloromethane, Ethyl Acetate

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