| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
sales8178@energy-chemical.com |
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| | O-tert-Butylhydroxylamine hydrochloride Basic information |
| | O-tert-Butylhydroxylamine hydrochloride Chemical Properties |
| Melting point | 158-159 °C(lit.) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | H2O: soluble0.5g/10 mL | | form | powder to crystal | | color | White to Almost white | | Water Solubility | H2O: soluble 0.5g/10 mL | | BRN | 3668106 | | InChI | InChI=1S/C4H11NO.ClH/c1-4(2,3)6-5;/h5H2,1-3H3;1H | | InChIKey | ZBDXGNXNXXPKJI-UHFFFAOYSA-N | | SMILES | C(C)(C)(C)ON.Cl |
| Hazard Codes | F | | Risk Statements | 11 | | RIDADR | UN 1325 4.1/PG 3 | | WGK Germany | 3 | | F | 10 | | HazardClass | 4.1 | | PackingGroup | Ⅲ | | HS Code | 29280090 | | Storage Class | 4.1B - Flammable solid hazardous materials | | Hazard Classifications | Flam. Sol. 2 |
| | O-tert-Butylhydroxylamine hydrochloride Usage And Synthesis |
| Chemical Properties | White crystalline powder | | Uses | Reactant involved in synthesis of biologically active molecules including:• ;CGS 25966 derivatives for use as MMP inhibitors1• ;Imidazolidinedione derivatives for use as antimalarial treatments2• ;Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists3• ;Rab proteins for isoprenylation and geranylgeranylation inhibition4Reactant involved in:• ;Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents5• ;Double allylic alkylation of indole-2-hydroxamates6• ;SN2 substitution reactions at amide nitrogens7• ;Photoc | | Uses | O-tert-Butylhydroxylamine Hydrochloride is an reactant used in various synthesis of biologically active molecules such as camptothecin derivatives that exerts anti-tumor activity, oxime derivatives as
GPR119 agonists and their preparation and highly Potent Matrix Metalloproteinase Inhibitors. | | Uses | Reactant involved in synthesis of biologically active molecules including:
- CGS 25966 derivatives for use as MMP inhibitors
- Imidazolidinedione derivatives for use as antimalarial treatments
- Pyrimidine ribonucleotide analogs as P2Y6 receptor agonists
- Rab proteins for isoprenylation and geranylgeranylation inhibition
Reactant involved in:
- Synthesis of N-(arylethyl)-O-tert-butylhydroxamates for use as Weinreb amide equivalents
- Double allylic alkylation of indole-2-hydroxamates
- SN2 substitution reactions at amide nitrogens
- Photocycloaddition to C=N bonds for synthesis of 1,3-diazepines
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| | O-tert-Butylhydroxylamine hydrochloride Preparation Products And Raw materials |
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