CAS 51537-21-4|H-Ser(tBu)-OtBu.HCl
Introduction：Basic information about CAS 51537-21-4|H-Ser(tBu)-OtBu.HCl, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | H-Ser(tBu)-OtBu.HCl | ||
|---|---|---|---|
| CAS Number | 51537-21-4 | Molecular Weight | 253.766 |
| Density | 0.969g/cm3 | Boiling Point | 283.8ºC at 760mmHg |
| Molecular Formula | C11H24ClNO3 | Melting Point | 155 °C(dec.) |
| MSDS | ChineseUSA | Flash Point | 81.3ºC |
Names
| Name | h-ser(tbu)-otbu hcl |
|---|---|
| Synonym | More Synonyms |
H-Ser(tBu)-OtBu.HCl BiologicalActivity
| Description | H-Ser(tBu)-OtBu.HCl is a serine derivative[1]. |
|---|---|
| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
| 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]. |
| 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. |
Chemical & Physical Properties
| Density | 0.969g/cm3 |
|---|---|
| Boiling Point | 283.8ºC at 760mmHg |
| Melting Point | 155 °C(dec.) |
| Molecular Formula | C11H24ClNO3 |
| Molecular Weight | 253.766 |
| Flash Point | 81.3ºC |
| Exact Mass | 253.144470 |
| PSA | 61.55000 |
| LogP | 2.97280 |
| Index of Refraction | 1.447 |
| InChIKey | RDWZQVGVBTYCBD-QRPNPIFTSA-N |
| SMILES | CC(C)(C)OCC(N)C(=O)OC(C)(C)C.Cl |
| Storage condition | Store at 0-5°C |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
Articles4
More Articles| Structure and synthesis of an immunoactive lipopeptide, WS1279, of microbial origin. Chem. Pharm. Bull. 39 , 607, (1991) The structure of WS1279, isolated from Streptomyces sp. as an immunoactive lipopeptide, has been deduced on the basis of chemical and physical evidence as S-[2,3-bis(palmitoyloxy)propyl]-N alpha-palmi... | |
| Chemical synthesis and surface activity of lung surfactant phospholipid analogs. III. Chiral N-substituted ether-amide phosphonolipids. Chem. Phys. Lipids 58 , 81, (1991) A homologous series of chiral (R) ether-amide phosphonolipid analogs of naturally occurring (R) glycerophospholipids were synthesized and characterized for their interfacial behaviors. The phosphonoli... | |
| H. Paulsen, K. Adermann Liebigs Ann. Chem. , 751, (1989) |
Synonyms
| H-Ser(tBu)-OtBu*HCl |
| O-tert-Butyl-L-serine tert-butyl ester hydrochloride |
| O-TERT-BUTYL-L-SERINE TERT-BUTYL ESTER HCL |
| 2-Methyl-2-propanyl O-(2-methyl-2-propanyl)-L-serinate hydrochloride (1:1) |
| H-L-SER(TBU)-OTBU HCL |
| O-t-butyl-DL-serine t-butyl ester hydrochloride |
| O-tert-Butyl-L-serine-butyl ester hydrochloride |
| MFCD00034850 |
| L-Serine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester, hydrochloride (1:1) |
| O-tert-Butylserine tert-butyl ester hydrochloride |
| Ser(tBu)-OtBu.HCl |
| H-SER(BUT)-OBUT HCL |
| L-serine tert-butyl ether tert-butyl ester hydrochloride |
| O-TERT-BUTYL-L-SERINE T-BUTYL ESTER HYDROCHLORIDE |
| tert-butyl O-(tert-butyl)-L-serinate hydrochloride |
| O-T-BUTYL-L-SERINE T-BUTYL ESTER HYDROCHLORIDE |
| DL-3-(t-Butoxy)alanine t-butyl ester hydrochloride |
| H-Ser(But)-ObutHCl |
