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Trimethyl(3-(trifluoromethoxy)phenyl)silane
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Trimethyl(3-(trifluoromethoxy)phenyl)silane
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 059209-5G , MDL Number: MFCD09816108
Supplier:
AMBEED, INC
Description:
Carbonyl Cyanide 4-(Trifluoromethoxy)phenylhydrazone, Purity: 98%, CAS Number: 370-86-5, Appearance: Form: Crystal - Powder / Colour: Pale yellow - Yellow, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 10MG
Supplier:
ALADDIN SCIENTIFIC
Description:
It is a tertiary amide having bulky N-groups. Its reduction to the corresponding amine, by reaction with silane in the presence of MoO2Cl2 (catalyst), has been reported.. Reactant for preparation of triazolothiadiazepine dioxide derivatives . Reactant for preparation of halo-substituted aromatic amides . Reactant for preparation of [[(phenyl)piperazinyl]alkyl]indolyl]ethanone and [[[(phenoxyethyl)piperazinyl]alkyl]indolyl]ethanone derivatives as α1-adrenoreceptor antagonists . Reactant for synthesis of naphthalenedione derivatives as antimycobacterial agents . Reactant for regioselective ortho Suzuki-Miyaura coupling reaction It may be used in the synthesis of 5-chloroindole.
Supplier:
AMBEED, INC
Description:
N-((1-Methylpiperidin-4-yl)methyl)-3-(3-(trifluoromethoxy)phenyl)imidazo[1,2-b]pyridazin-6-amine, Purity: 99+%, CAS Number: 1025065-69-3, Appearance: White to light-yellow solid, Storage: Keep in dark place, Inert atmosphere, Store in freezer, under -20 C, Size: 1mg
Supplier:
AMBEED, INC
Description:
GNF-5 98%
Supplier:
AMBEED, INC
Description:
rel-2-((1R,3r,5S)-3-((5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazol-4-yl)methoxy)-8-azabicyclo[3.2.1]octan-8-yl)-4-fluorobenzo[d]thiazole-6-carboxylic acid, Purity: 98%, CAS Number: 1383816-29-2, Appearance: White to yellow powder or crystals, Storage: Keep in dark place, 2-8C, Size: 50MG
Supplier:
AMBEED, INC
Description:
2-Methoxy-5-trifluoromethoxyphenylboronic acid pinacol ester ≥95%
Supplier:
TCI America
Description:
CAS Number: 50823-90-0
MDL Number: MFCD00061270 Molecular Formula: C8H7F3O2 Molecular Weight: 192.14 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Color: Colorless Specific Gravity (20/20): 1.32
Supplier:
AOB CHEM USA
Description:
2-Methoxy-5-trifluoromethoxyphenylboronic acid pinacol ester ≥97%
Catalog Number:
(TCT2593-1G)
Supplier:
TCI America
Description:
CAS Number: 175278-07-6
MDL Number: MFCD00153285 Molecular Formula: C8H7F3O2 Molecular Weight: 192.14 Purity/Analysis Method: >96.0% (GC) Form: Clear Liquid Color: Very Pale Yellow Boiling point (°C): 98 Specific Gravity (20/20): 1.33
Supplier:
TCI America
Description:
CAS Number: 170141-63-6
MDL Number: MFCD00042403 Molecular Formula: C9H7F3O2 Molecular Weight: 204.15 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Color: Colorless Flash Point (°C): 83 Specific Gravity (20/20): 1.29
Supplier:
Adipogen
Description:
Potent protein kinase VEGFR2 inhibitor (2nm range). Binds to the pseudokinase domain of MLKL and blocks cell death by necroptosis, as well. With regards to its role in necroptosis, it is an ATP-mimetic that was shown to bind recombinant mouse MLKL pseudokinase domain, which showed inhibited TSQ-induced death of mouse dermal fibroblasts by delaying MLKL translocation to the membrane. Appears therefore to be a valuable reagent to inhibit necroptosis. It also provides an important proof-of-principle that targeting catalytically-dead pseudoenzymes represents a feasible, emerging therapeutic avenue.
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Catalog Number:
(89149-264)
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
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