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CAS RN: 2265-92-1 | Product Number: D3594
1,4-Difluoro-2-iodobenzene
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Purity: >98.0%(GC)
Synonyms:
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
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|---|---|---|---|---|---|
| 1G |
A$52.00
|
11 | 0 | It can be shipped in about 2 weeks after ordering |
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| Product Number | D3594 |
| Purity / Analysis Method | >98.0%(GC) |
| Molecular Formula / Molecular Weight | C__6H__3F__2I = 239.99 |
| Physical State (20 deg.C) | Liquid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Condition to Avoid | Light Sensitive |
| CAS RN | 2265-92-1 |
| Reaxys Registry Number | 2081101 |
| PubChem Substance ID | 87559832 |
| MDL Number | MFCD03094151 |
Specifications
| Appearance | Colorless to Light yellow to Light red clear liquid |
| Purity(GC) | min. 98.0 % |
| NMR | confirm to structure |
Properties (reference)
| Boiling Point | 183 °C |
| Flash point | 85 °C |
| Specific Gravity (20/20) | 2.01 |
| Refractive Index | 1.56 |
GHS
| Pictogram |
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| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. H227 : Combustible liquid. |
| Precautionary Statements | P501 : Dispose of contents/ container to an approved waste disposal plant. P210 : Keep away from heat/sparks/open flames/hot surfaces. No smoking. P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. P403 + P235 : Store in a well-ventilated place. Keep cool. |
Related Laws:
Transport Information:
| H.S.code* | 2903.99-000 |
Application
Dorsomorphin (Compound C): An Inhibitor of BMP Sinnaling and AMPK
Dorsomorphin (Compound C) is used as an inhibitor of bone morphogenetic protein (BMP) signaling, and an inhibitor of AMP-activated protein kinase (AMPK).
BMP plays a fundamental role in the regulation of bone organogenesis through the activation of receptor serine/threonine kinases, and BMP signaling regulates many different biological processes, including cell growth, differentiation, and embryogenesis. Dorsomorphin inhibit the BMP signaling.
AMP-activated protein kinase (AMPK), a serine/threonine kinase, is an evolutionarily conserved energy sensor important for cell growth, proliferation, survival, and metabolic regulation. Dorsomorphin (Compound C) also inhibits the AMPK.
BMP plays a fundamental role in the regulation of bone organogenesis through the activation of receptor serine/threonine kinases, and BMP signaling regulates many different biological processes, including cell growth, differentiation, and embryogenesis. Dorsomorphin inhibit the BMP signaling.
AMP-activated protein kinase (AMPK), a serine/threonine kinase, is an evolutionarily conserved energy sensor important for cell growth, proliferation, survival, and metabolic regulation. Dorsomorphin (Compound C) also inhibits the AMPK.
References
- Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism
- Small-molecule dissection of BMP signaling (a review)
- Compound C inhibits hypoxic activation of HIF-1 independent of AMPK
- Compound C induces protective autophagy in cancer cells through AMPK inhibition-independent blockade of Akt/mTOR pathway
- The AMPK Inhibitor Compound C Is a Potent AMPK-Independent Antiglioma Agent
PubMed Literature
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Safety Data Sheet (SDS)
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Specifications
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