Introduction：Basic information about CAS 31687-58-8|Boc-His(Boc)-OH DCHA, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Boc-His(Boc)-OH DCHA |
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| CAS Number | 31687-58-8 | Molecular Weight | 536.70400 |
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| Density | / | Boiling Point | 679.7ºC at 760 mmHg |
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| Molecular Formula | C28H48N4O6 | Melting Point | 160-165ºC (dec.) |
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| MSDS | / | Flash Point | 364.9ºC |
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Names
| Name | N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[1-[(2-methylpropan-2-yl)oxycarbonyl]imidazol-4-yl]propanoic acid |
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| Synonym | More Synonyms |
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Boc-His(Boc)-OH DCHA BiologicalActivity
| Description | Boc-His(Boc)-OH.DCHA is a histidine 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
| Boiling Point | 679.7ºC at 760 mmHg |
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| Melting Point | 160-165ºC (dec.) |
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| Molecular Formula | C28H48N4O6 |
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| Molecular Weight | 536.70400 |
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| Flash Point | 364.9ºC |
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| Exact Mass | 536.35700 |
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| PSA | 131.78000 |
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| LogP | 6.20990 |
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| InChIKey | WBGMQHNUPJENDC-MERQFXBCSA-N |
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| SMILES | C1CCC(NC2CCCCC2)CC1.CC(C)(C)OC(=O)NC(Cc1cn(C(=O)OC(C)(C)C)cn1)C(=O)O |
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| Storage condition | -20°C |
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Safety Information
| Hazard Codes | Xn |
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| Safety Phrases | 22-24/25 |
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| WGK Germany | 3 |
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Synonyms
| Boc-L-His(Boc)*DCHA |
| Boc-His(Boc)-OH DCHA |
| Boc-His(Boc).DCHA |
| Boc-His(Boc)-OH (dicyclohexylammonium) salt |
| Boc-His(Boc)-OH DCH |
| EINECS 250-764-6 |
| Boc-His(Boc)-OH dicyclohexylamine salt |
| N,1-Bis(Boc)-L-histidine dicyclohexylamine salt |
| BOC-HIS(BOC)-OH DCHA |
| Boc(Nim-Boc)His-OH*DCHA |
| Boc-His(Boc)-OH·DCHA |
