Introduction：Basic information about CAS 336817-91-5|BOC--(4-BROMBENZYL)-DL-PRO-OH, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | BOC--(4-BROMBENZYL)-DL-PRO-OH |
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| CAS Number | 336817-91-5 | Molecular Weight | 384.26500 |
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| Density | 1.412g/cm3 | Boiling Point | 488.6ºC at 760 mmHg |
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| Molecular Formula | C17H22BrNO4 | Melting Point | / |
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| MSDS | ChineseUSA | Flash Point | 249.3ºC |
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Names
| Name | 2-[(4-bromophenyl)methyl]-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid |
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| Synonym | More Synonyms |
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BOC--(4-BROMBENZYL)-DL-PRO-OH BiologicalActivity
| Description | Boc-α-(4-bromobenzyl)-DL-Pro-OH is a proline derivative[1]. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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| In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
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| References | [1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144. |
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Chemical & Physical Properties
| Density | 1.412g/cm3 |
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| Boiling Point | 488.6ºC at 760 mmHg |
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| Molecular Formula | C17H22BrNO4 |
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| Molecular Weight | 384.26500 |
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| Flash Point | 249.3ºC |
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| Exact Mass | 383.07300 |
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| PSA | 66.84000 |
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| LogP | 3.78380 |
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| Index of Refraction | 1.573 |
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| InChIKey | VQWRXYZZPMLJRL-UHFFFAOYSA-N |
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| SMILES | CC(C)(C)OC(=O)N1CCCC1(Cc1ccc(Br)cc1)C(=O)O |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| RIDADR | NONH for all modes of transport |
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Synonyms
| Boc-|A-(4-bromobenzyl)-DL-proline |
| N-(tert-butoxycarbonyl)-2-(4-bromobenzyl)proline |
| 2-(4-bromobenzyl)-1-(tert-butoxycarbonyl)proline |
| Boc-|A-(4-bromobenzyl)-DL-Pro-OH |
| 1-Boc-2-(4-bromobenzyl)-2-pyrrolidinecarboxylic acid |
