ChemicalBook--->CAS DataBase List--->39684-28-1

39684-28-1

39684-28-1 Structure

39684-28-1 Structure
IdentificationBack Directory
[Name]

O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
[CAS]

39684-28-1
[Synonyms]

O-(tert-Butyl)
LABOTEST-BB LT00233214
O-Tert-ButylhydroxylamineHCl
tert-Butoxyamine hydrochloride
O-T-BUTYLHYDROXYLAMINE HYDROCHLORIDE
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE
2-Aminooxy-2-methylpropane hydrochloride
O-(tert-Butyl)hydroxylamine hydrochloride,99%
O-(1,1-Dimethylethyl)hydroxylamine hydrochloride
O-tert-ButylhydroxylaMine hydrochloride >=99.0% (AT)
HydroxylaMine,O-(1,1-diMethylethyl)-, hydrochloride (1:1)
[EINECS(EC#)]

254-590-1
[Molecular Formula]

C4H12ClNO
[MDL Number]

MFCD00043272
[MOL File]

39684-28-1.mol
[Molecular Weight]

125.6
Chemical PropertiesBack Directory
[Appearance]

White crystalline powder
[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 InformationBack Directory
[Chemical Properties]

White crystalline powder
[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 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
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)
GHS02
[Signal word ]

Warning
[Hazard statements ]

H228
[Precautionary statements ]

P210
[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
Spectrum DetailBack Directory
[Spectrum Detail]

O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE(39684-28-1)1HNMR
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE(39684-28-1)IR
O-TERT-BUTYLHYDROXYLAMINE HYDROCHLORIDE(39684-28-1)Raman
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