L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester
Glu(OtBu)-OMe.HCl
CAS: 5854-78-4
Molecular Formula: C12H25NO3
L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester - Names and Identifiers
| Name | Glu(OtBu)-OMe.HCl |
| Synonyms | H-Thr(Tbu)-Otbu H-Thr(otbu)otbu H-Thr(tBu)-OtBu H-THR(TBU)-OTBU Glu(OtBu)-OMe.HCl THREONINE(TBU)-OTBU O-T-BUTYL-L-THREONINE T-BUTYL ESTER O-TERT-BUTYL-L-THREONINET-BUTYLESTER tert-Butyl O-tert-butyl-L-threoninate O-TERT-BUTYL-L-THREONINE TERT-BUTYL ESTER O-tert-Butyl-L-threonine tert-Butyl Ester (2S,3R)-tert-Butyl 2-aMino-3-(tert-butoxy)butanoate L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester |
| CAS | 5854-78-4 |
| InChI | InChI=1/C12H25NO3/c1-8(15-11(2,3)4)9(13)10(14)16-12(5,6)7/h8-9H,13H2,1-7H3/t8-,9+/m1/s1 |
| InChIKey | PPDIUNOGUIAFLV-BDAKNGLRSA-N |
L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester - Physico-chemical Properties
| Molecular Formula | C12H25NO3 |
| Molar Mass | 231.33 |
| Density | 0.959±0.06 g/cm3(Predicted) |
| Melting Point | 74-75 °C |
| Boling Point | 70°C/0.8mmHg(lit.) |
| Flash Point | 79.3°C |
| Vapor Presure | 0.00146mmHg at 25°C |
| Appearance | clear liquid |
| Color | Colorless to Red to Green |
| pKa | 6.14±0.33(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,Store in freezer, under -20°C |
| Refractive Index | 1.4320-1.4360 |
| MDL | MFCD00077109 |
L-threonine, O-(1,1-dimethylethyl)-, 1,1-dimethylethyl ester - Introduction
Glu(OtBu)-OMe. HCl (Glu(OtBu)-OMe.HCl) is an organic compound with the following main properties:
1. Appearance: Usually a white crystalline solid.
2. solubility: soluble in polar solvents, such as methanol, ethanol and dimethyl sulfoxide.
3. stability: relatively stable at room temperature, but need to avoid light preservation.
Glu(OtBu)-OMe. HCl is widely used in the field of organic synthesis, and its main uses are as follows:
1. as a reagent for protecting amino acids: because its molecule contains tBu protecting group, it can protect the amino group on valine to prevent accidental chemical reaction during the reaction.
2. Synthetic valine receptor agonist: due to Glu(OtBu)-OMe. The valine-containing moiety in the HCl structure can be used to synthesize valine analogs for drug development.
Glu(OtBu)-OMe. The preparation method of HCl can generally be carried out by the method of organic synthesis, and specific steps can be optimized according to specific needs.
For safety information, Glu(OtBu)-OMe. The specific safety assessment of HCl needs to be carried out according to specific experimental conditions and uses. In general, the handling of organic compounds should comply with general laboratory safety practices, such as wearing appropriate protective equipment, avoiding contact with skin and eyes, and maintaining a well-ventilated laboratory environment. In addition, appropriate treatment and disposal should be carried out in accordance with relevant laws and regulations. It is recommended to consult the relevant safety data sheets and technical literature before use to ensure the safety of operation.
1. Appearance: Usually a white crystalline solid.
2. solubility: soluble in polar solvents, such as methanol, ethanol and dimethyl sulfoxide.
3. stability: relatively stable at room temperature, but need to avoid light preservation.
Glu(OtBu)-OMe. HCl is widely used in the field of organic synthesis, and its main uses are as follows:
1. as a reagent for protecting amino acids: because its molecule contains tBu protecting group, it can protect the amino group on valine to prevent accidental chemical reaction during the reaction.
2. Synthetic valine receptor agonist: due to Glu(OtBu)-OMe. The valine-containing moiety in the HCl structure can be used to synthesize valine analogs for drug development.
Glu(OtBu)-OMe. The preparation method of HCl can generally be carried out by the method of organic synthesis, and specific steps can be optimized according to specific needs.
For safety information, Glu(OtBu)-OMe. The specific safety assessment of HCl needs to be carried out according to specific experimental conditions and uses. In general, the handling of organic compounds should comply with general laboratory safety practices, such as wearing appropriate protective equipment, avoiding contact with skin and eyes, and maintaining a well-ventilated laboratory environment. In addition, appropriate treatment and disposal should be carried out in accordance with relevant laws and regulations. It is recommended to consult the relevant safety data sheets and technical literature before use to ensure the safety of operation.
Last Update：2024-04-09 21:04:16
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Product Name: O-Tert-Butyl-L-Threonine Tert-Butyl Ester Visit Supplier Webpage Request for quotation
CAS: 5854-78-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 5854-78-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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