Boc-Cyclolencine structure 
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        Common Name | Boc-Cyclolencine | ||
|---|---|---|---|---|
| CAS Number | 35264-09-6 | Molecular Weight | 229.27 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 382.5±31.0 °C at 760 mmHg | |
| Molecular Formula | C11H19NO4 | Melting Point | 130-135 °C | |
| MSDS | Chinese USA | Flash Point | 185.1±24.8 °C | |
            Use of Boc-CyclolencineBoc-Cycloleucine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.  | 
    
| Name | 1-[(2-methylpropan-2-yl)oxycarbonylamino]cyclopentane-1-carboxylic acid | 
|---|---|
| Synonym | More Synonyms | 
| Description | Boc-Cycloleucine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | 
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| Related Catalog | 
| Density | 1.2±0.1 g/cm3 | 
|---|---|
| Boiling Point | 382.5±31.0 °C at 760 mmHg | 
| Melting Point | 130-135 °C | 
| Molecular Formula | C11H19NO4 | 
| Molecular Weight | 229.27 | 
| Flash Point | 185.1±24.8 °C | 
| Exact Mass | 229.131409 | 
| PSA | 75.63000 | 
| LogP | 1.47 | 
| Vapour Pressure | 0.0±1.9 mmHg at 25°C | 
| Index of Refraction | 1.495 | 
| Water Solubility | Soluble in hot water | 
| HS Code | 2924299090 | 
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% | 
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                                    New alpha-thiol dipeptide dual inhibitors of angiotensin-I converting enzyme and neutral endopeptidase EC 3.4.24.11.
                                    
                                    
                                     J. Med. Chem. 38 , 5023, (1995) Dual inhibitors of the two zinc metallopeptidases, neutral endopeptidase (NEP, EC 3.4.24.11) and angiotensin-I converting enzyme, have been the focus of much clinical interest for the treatment of hyp...  | 
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                                    Conformational versatility of the N alpha-acylated tripeptide amide tail of oxytocin. Synthesis and crystallographic characterization of three C2 alpha-backbone modified, conformationally restricted analogues.
                                    
                                    
                                     Int. J. Pept. Protein Res. 42 , 459, (1993) The synthesis, physical and analytical characterization, and crystal-state structural analysis by X-ray diffraction of three analogues of the N alpha-acylated tripeptide amide tail of oxytocin, each c...  | 
                                
| Boc-1-aminocyclopentane-1-carboxylic acid | 
| Boc-Cycloleucine | 
| 1-(tert-Butoxycarbonylamino)cyclopentanecarboxylic Acid | 
| Cyclopentanecarboxylic acid, 1-[[(1,1-dimethylethoxy)carbonyl]amino]- | 
| 1-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)cyclopentanecarboxylic acid | 
| Cyclopentanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]- | 
| N-Boc-1-amino-1-cyclopentanecarboxylic acid | 
| 2-tert-Butoxycarbonylamino-cyclopentanecarboxylic acid | 
| MFCD01076126 | 
| 1-N-Boc-Aminocyclopentanecarboxylic Acid | 
| 1-N-Boc-Aminocyclopentanecarboxylicacid | 
| Boc-Cyclolencine | 
| N-Boc-cycloleucine | 
| 1-[(tert-Butoxycarbonyl)amino]cyclopentanecarboxylic acid | 
| 1-(Boc-amino)cyclopentanecarboxylic acid | 
| 2-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)cyclopentanecarboxylic acid | 
| 1-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid |