| Identification | More | [Name]
2-Bromo-4'-methoxyacetophenone | [CAS]
2632-13-5 | [Synonyms]
2-BROMO-1-(4-METHOXYPHENYL)ETHAN-1-ONE
2-BROMO-1-(4-METHOXYPHENYL)ETHANONE
2-BROMO-4-METHOXY ACETOPHENONE
4-(BROMOACETYL)ANISOLE
4-METHOXYPHENACYL BR
4'-METHOXYPHENACYL BROMIDE
4-METHOXYPHENACYL BROMIDE
4-methoxy phenecyl bromide
A-BROMO-P-METHOXYACETOPHENONE
AKOS BBS-00000817
ALPHA-BROMO-4'-METHOXYACETOPHENONE
ALPHA-BROMO-4-METHOXYACETOPHENONE
Bromomethyl 4-methoxyphenyl ketone
OMEGA-BROMO-4-METHOXYACETOPHENONE
OMEGA-BROMO-P-METHOXY ACETOPHENONE
P-METHOXYPHENACYL BROMIDE
PROTEIN TYROSINE PHOSPHATASE INHIBITOR II
TIMTEC-BB SBB007777
W-BROMO-4-METHOXY-ACETOPHENONE
2-(4-Methoxyphenyl)-2-oxoethyl bromide | [EINECS(EC#)]
220-118-8 | [Molecular Formula]
C9H9BrO2 | [MDL Number]
MFCD00465443 | [Molecular Weight]
229.07 | [MOL File]
2632-13-5.mol |
| Chemical Properties | Back Directory | [Appearance]
off-white to light brown crystals or | [Melting point ]
69-71 °C(lit.) | [Boiling point ]
215.8°C (rough estimate) | [density ]
1.4921 (rough estimate) | [refractive index ]
1.5500 (estimate) | [storage temp. ]
2-8°C
| [solubility ]
Chloroform (Slightly), Methanol (Slightly) | [form ]
Crystals or Crystalline Powder | [color ]
Off-white to light brown | [Water Solubility ]
It is soluble in DMSO, water (partly miscible), most organic solvents, and methanol. | [BRN ]
743112 | [InChI]
InChI=1S/C9H9BrO2/c1-12-8-4-2-7(3-5-8)9(11)6-10/h2-5H,6H2,1H3 | [InChIKey]
XQJAHBHCLXUGEP-UHFFFAOYSA-N | [SMILES]
C(=O)(C1=CC=C(OC)C=C1)CBr | [CAS DataBase Reference]
2632-13-5(CAS DataBase Reference) | [NIST Chemistry Reference]
Ethanone, 2-bromo-1-(4-methoxyphenyl)-(2632-13-5) |
| Safety Data | Back Directory | [Hazard Codes ]
C,Xi | [Risk Statements ]
R34:Causes burns.
R36/37:Irritating to eyes and respiratory system .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S27:Take off immediately all contaminated clothing .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 3261 8/PG 2
| [WGK Germany ]
3
| [F ]
8-9-19-21 | [Hazard Note ]
Corrosive | [HazardClass ]
8 | [PackingGroup ]
III | [HS Code ]
29147090 |
| Hazard Information | Back Directory | [Chemical Properties]
off-white to light brown crystals or | [Uses]
2-Bromo-4'-methoxyacetophenone is a α-haloacetophenone derivatives tested for inhibition of protein tyrosine phosphatases SHP-1 and PTP1B. | [Uses]
2-Bromo-4'-methoxyacetophenone, is used as a cell-permeable, covalent and potent protein tyrosine phosphatase inhibitor. | [Preparation]
Obtained by reaction of N-bromosuccinimide (NBS) with 4-methoxyacetophenone in the presence of trimethylsilyl trifluoromethanesulfonate (TMS-OTf) in acetonitrile at r.t. for 24 h (87%). | [Biological Activity]
ki: 128 μmptp inhibitor ii is a protein tyrosine phosphatase (ptp) inhibitor.protein tyrosine phosphatases (ptps) are reported to be involved in the etiology of diabetes mellitus, neural diseases such as alzheimer and parkinson diseases, regulation of allergy and inflammation, or ptps are even regarded to be responsible for the pathogens. | [in vitro]
in a previous study, it was found that all of the previously reported ptp inhibitors contained a negatively charged, nonhydrolyzable py mimetic as the core structure, such as malonates, aryl carboxylates, phosphonates, or cinnamates. the poor membrane permeability of these inhibitors might compromise their potential development. it was reported that several α-bromoacetophenone derivatives, such as ptp inhibitor ii, could act as fairly potent ptp inhibitors, by covalently alkylating the conserved catalytic cysteine in the ptp active site. since ptp inhibitor ii is neutral, it could readily diffuse into human b cells and inhibit the intracellular ptps. the sar study was performed with the catalytic domain of phosphatase shp-1, and ti was found that ptp inhibitor ii showed time-dependent inactivation of shp-1, consistent with the mechanism. furthermore, the potency of ptp inhibitor ii was described by an equilibrium constant ki, representing the dissociation constant of the noncovalent enzyme–inhibitor complex. ptp inhibitor ii bound with lower affinity than ptp inhibitor i with ki values of 128 μm [1]. | [storage]
Room temperature | [References]
[1] p. heneberg. use of protein tyrosine phosphatase inhibitors as promising targeted therapeutic drugs. current medicinal chemistry 16(6), 706-733 (2009). |
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