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CAS RN: 83249-10-9 | Product Number: M3149
3-(Methoxycarbonyl)bicyclo[1.1.1]pentane-1-carboxylic Acid
Purity: >97.0%(T)
Synonyms:
- Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acid 1-Monomethyl Ester
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
200MG |
$34.00
|
7 | 1 |
1G |
$118.00
|
4 | 2 |
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Product Number | M3149 |
Purity / Analysis Method | >97.0%(T) |
Molecular Formula / Molecular Weight | C__8H__1__0O__4 = 170.16 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
Packaging and Container | 1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 83249-10-9 |
Reaxys Registry Number | 4310400 |
PubChem Substance ID | 468592296 |
MDL Number | MFCD20638314 |
Specifications
Appearance | White to Orange to Green powder to crystal |
Purity(GC) | min. 95.0 % |
Purity(Neutralization titration) | min. 97.0 % |
Melting point | 138.0 to 142.0 °C |
Properties (reference)
Melting Point | 140 °C |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. 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. |
Related Laws:
Transport Information:
H.S.code* | 2917.20-000 |
Application
A Building Block for Bioisosteric Replacement of Aromatic Groups
This product is belong to bicyclo[1.1.1]pentanes which have recently been reported in the scientific literature as useful chemical tools for bioisosteric replacement of aromatic groups. Therefore, bicyclo[1.1.1]pentanes are now used in drug discovery research, and the demand for these building blocks is growing exponentially.
References
- Application of the Bicyclo[1.1.1]pentane Motif as a Nonclassical Phenyl Ring Bioisostere in the Design of a Potent and Orally Active γ-Secretase Inhibitor
- Toward Resolving the Resveratrol Conundrum: Synthesis and in Vivo Pharmacokinetic Evaluation of BCP-Resveratrol
- Investigation of a Bicyclo[1.1.1]pentane as a Phenyl Replacement within an LpPLA2 Inhibitor
- Pharmaceuticals that contain polycyclic hydrocarbon scaffolds (a review)
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