CAS Number850568-54-6
Synonyms[4-(tert-Butoxycarbonyl)phenyl]boronic acid; 4-(tert-Butoxycarbonyl)phenylboronic acid; 4-(T-Butoxycarbonyl)phenylboronicacid; (4-{[(2-Methyl-2-propanyl)oxy]carbonyl}phenyl)boronic acid; [4-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]boronic acid; Benzoic acid, 4-borono-, 1,1-dimethylethyl ester
Molecular FormulaC11H15O4B1
Molecular Weight222.05
Density1.2±0.1 g/cm3
Boiling Point364.3±44.0 °C at 760 mmHg
Melting Point128-132ºC
AppearanceSolid;White to Almost white powder to crystal
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 850568-54-6 |
| Catalog No. | 2A-9068722 |
| Chinese Name | 4-(叔丁氧羰基)苯硼酸 |
| Synonyms | [4-(tert-Butoxycarbonyl)phenyl]boronic acid; 4-(tert-Butoxycarbonyl)phenylboronic acid; 4-(T-Butoxycarbonyl)phenylboronicacid; (4-{[(2-Methyl-2-propanyl)oxy]carbonyl}phenyl)boronic acid; [4-[(2-methylpropan-2-yl)oxycarbonyl]phenyl]boronic acid; Benzoic acid, 4-borono-, 1,1-dimethylethyl ester |
| Molecular Formula | C11H15O4B1 |
| Molecular Weight | 222.05 |
| Density | 1.2±0.1 g/cm3 |
| Boiling Point | 364.3±44.0 °C at 760 mmHg |
| Melting Point | 128-132ºC |
| Appearance | Solid;White to Almost white powder to crystal |
| Storage Condition | room temperature |
| Application | (4-(tert-Butoxycarbonyl)phenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound in life science-related research. |
| HTC | 2931900090 |
| MDL Number | MFCD03411946 |
| SMILES | CC(C)(C)OC(=O)c1ccc(B(O)O)cc1 |
| InChI | InChI=1S/C11H15BO4/c1-11(2,3)16-10(13)8-4-6-9(7-5-8)12(14)15/h4-7,14-15H,1-3H3 |
| InChI Key | QMVMDYSTJSUDKC-UHFFFAOYSA-N |
| MSDS | msds/68722_1_850568_54_6.pdf |
| Bioactivity | (4-(tert-Butoxycarbonyl)phenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others In Vitro Phenylboronic acid mediates ortho-specific hydroxyalkylation of phenols by aldehydes. The ability of boronic acid to reversibly bind diol functional groups has been exploited for the fluorescence detection of sugars. It can be an effective catalyst for amidation and esterification of carboxylic acids. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 364.3±44.0 °C at 760 mmHg Melting Point 128-132ºC Molecular Formula C11H15BO4 Molecular Weight 222.05 Flash Point 174.1±28.4 °C Exact Mass 222.106339 PSA 66.76000 LogP 2.80 Vapor Pressure 0.0±0.9 mmHg at 25°C Index of Refraction 1.517 InChIKey QMVMDYSTJSUDKC-UHFFFAOYSA-N SMILES CC(C)(C)OC(=O)c1ccc(B(O)O)cc1 |
| Use of | (4-(tert-Butoxycarbonyl)phenyl)boronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Related Catalog Research Areas >> Others In Vitro Phenylboronic acid mediates ortho-specific hydroxyalkylation of phenols by aldehydes. The ability of boronic acid to reversibly bind diol functional groups has been exploited for the fluorescence detection of sugars. It can be an effective catalyst for amidation and esterification of carboxylic acids. Chemical & Physical Properties Molecular Formula C11H15BO4 Exact Mass 222.106339 PSA 66.76000 Index of Refraction 1.517 InChIKey QMVMDYSTJSUDKC-UHFFFAOYSA-N |
| Tax Rebate | 13.0% |
| Supervision | AB (Inbound cargo customs clearance form) |
| Transport Info | Product name: 4-(tert-butoxycarbonyl)phenylboronic acid (containing different amounts of anhydride) |
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