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N-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide
CAS No. 1098360-68-9
N-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide( —— )
Catalog No. M28422 CAS No. 1098360-68-9
N-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide is a chemical compound.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 85 | In Stock |
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| 5MG | 77 | In Stock |
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| 10MG | 116 | In Stock |
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| 25MG | 199 | In Stock |
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| 50MG | 282 | In Stock |
|
| 100MG | 384 | In Stock |
|
| 200MG | 510 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameN-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide
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NoteResearch use only, not for human use.
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Brief DescriptionN-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide is a chemical compound.
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DescriptionN-(4-bromo-2-chlorophenyl)-5-chloro-2-hydroxybenzamide is a chemical compound.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptorapolipoprotein L1
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Research Area——
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Indication——
Chemical Information
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CAS Number1098360-68-9
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Formula Weight361.02
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Molecular FormulaC13H8BrCl2NO2
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Purity>98% (HPLC)
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Solubility——
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SMILESOc1ccc(Cl)cc1C(=O)Nc1ccc(Br)cc1Cl
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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AQC
AQC (6-Aminoquinolyl-N-hydroxysccinimidyl carbamate) is a reagent for the fluorescence detection of amino acid or protein sequence by HPLC.
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WEHL-04
WEHL-04 is an intermediate used to prepare (isoquinolinylsulfonyl)benzoic acids as inhibitors of type 5 71-β-hydroxysteroid dehydrogenase AKR1C3. It is also used in the synthesis of 2-aminooctahydrocyclopentalene-3a-carboxamides as potent CCR2 antagonists.
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Amylin, amide, human
Amylin, a 37-amino acid polypeptide that is structurally related to calcitonin, is secreted from the B cells of the pancreas. Amylin has anoretic effects in rats. Amylin may be responsible for the etiology of insulin resistance of type II diabetes mellitus through its modulation of peripheral effects of insulin.
