20023
O-叔丁基羟胺 盐酸盐
≥99.0% (AT)
别名:
2-Aminooxy-2-methylpropane hydrochloride, O-(1,1-Dimethylethyl)hydroxylamine hydrochloride, tert-Butoxyamine hydrochloride
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About This Item
线性分子式:
(CH3)3CONH2 · HCl
CAS Number:
分子量:
125.60
Beilstein:
3668106
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
≥99.0% (AT)
表单
solid
mp
~155 °C (dec.)
溶解性
H2O: soluble 0.5 g/10 mL
SMILES字符串
Cl.CC(C)(C)ON
InChI
1S/C4H11NO.ClH/c1-4(2,3)6-5;/h5H2,1-3H3;1H
InChI key
ZBDXGNXNXXPKJI-UHFFFAOYSA-N
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应用
O-tert-Butylhydroxylamine hydrochloride was used in the synthesis of N-methyl-O-tert-butylhydroxylamine hydrochloride. It was also used in the preparation of N-tert-butoxyamino acids as substrates for the unambiguous synthesis of N-hydroxy peptides.
Reactant involved in synthesis of biologically active molecules including:
Reactant involved in:
- 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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