1257651-53-8
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Basic information
- Product Name: 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid
- Synonyms: 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid;3-Carboxyphenylboronic acid MIDA ester
- CAS NO:1257651-53-8
- Molecular Formula: C12H12BNO6
- Molecular Weight: 277.04
- EINECS: N/A
- Product Categories: N/A
- Mol File: 1257651-53-8.mol
- Article Data: 0
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Chemical Properties
- Melting Point: 253-258 °C
- Boiling Point: 428.6±55.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.39±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- PKA: 3.98±0.10(Predicted)
- CAS DataBase Reference: 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid(CAS DataBase Reference)
- NIST Chemistry Reference: 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid(1257651-53-8)
- EPA Substance Registry System: 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid(1257651-53-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 1257651-53-8(Hazardous Substances Data)
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1257651-53-8 Usage
Description
3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid is a chemical compound that features a benzoic acid core with a MIDA (Manganese Imidazole Diazoacetate) boronate group attached to the 3-position. 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid is characterized by its ability to participate in Suzuki cross-coupling reactions, a type of carbon-carbon bond formation widely used in organic synthesis.Used in Pharmaceutical Industry:
3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid is used as a synthetic intermediate for the development of pharmaceutical compounds. Its reactivity in Suzuki cross-coupling reactions allows for the creation of diverse and complex molecular structures, which can be further optimized for drug discovery and medicinal chemistry applications.
Used in Chemical Research:
In the field of chemical research, 3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid serves as a valuable building block for the synthesis of various organic compounds. Its unique structure and reactivity make it a useful tool for exploring new reaction pathways and developing novel synthetic methods.
Used in Material Science:
3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid can be utilized in the development of new materials with specific properties. Its ability to form carbon-carbon bonds through Suzuki cross-coupling can contribute to the creation of advanced polymers, coatings, and other materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1257651-53-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,6,5 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.Calculate Digit Verification of CAS Registry Number 1257651-53:
(9*1)+(8*2)+(7*5)+(6*7)+(5*6)+(4*5)+(3*1)+(2*5)+(1*3)=168
168 % 10 = 8
So 1257651-53-8 is a valid CAS Registry Number.
1257651-53-8Upstream product
1257651-53-8Downstream Products
- 1620064-12-1 C31H30FN3O4
- 1620064-17-6 6-amino-2-(4-fluorophenyl)-5-(3-((1-hydroxy-2-methylpropan-2-yl)carbamoyl)phenyl)-N-methylbenzofuran-3-carboxamide
- 1620064-16-5 2-(4-fluorophenyl)-5-(3-((1-hydroxy-2-methylpropan-2-yl)carbamoyl)phenyl)-N-methyl-6-nitrobenzofuran-3-carboxamide
- 1217335-93-7 3-(2-(4-fluorophenyl)-3-(methylcarbamoyl)-6-nitrobenzofuran-5-yl)benzoic acid
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3-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzoic acid
