O-Benzylhydroxylamine hydrochloride

O-Benzylhydroxylamine hydrochloride Basic information
Product Name:O-Benzylhydroxylamine hydrochloride
Synonyms:LABOTEST-BB LT00233131;BENZYLOXYAMINE HYDROCHLORIDE;BENZYLOXYAMINE HCL;TIMTEC-BB SBB003971;O-BENZYLHYDROXYLAMMONIUM CHLORIDE;O-BENZYLHYDROXYLAMINE HYDROCHLORIDE;O-BENZYLHYDROXYLAMINE CHLORHYDRATE;orthoBenzyl Hydroxylamine HCl
CAS:2687-43-6
MF:C7H10ClNO
MW:159.61
EINECS:220-249-0
Product Categories:Hydroxylamines;Hydroxylamines (O-Substituted);Amines;Aromatics;Pharmaceutical Intermediates;1
Mol File:2687-43-6.mol
O-Benzylhydroxylamine hydrochloride Structure
O-Benzylhydroxylamine hydrochloride Chemical Properties
Melting point 238 °C (subl.)(lit.)
storage temp. Inert atmosphere,2-8°C
solubility Soluble in DMSO and methanol.
form Crystalline Powder or Flakes
color White to almost white
PH2.2~3.2 (10g/l, 25℃)
Sensitive Hygroscopic
BRN 3595440
InChIInChI=1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H
InChIKeyHYDZPXNVHXJHBG-UHFFFAOYSA-N
SMILESC1(CON)=CC=CC=C1.Cl
CAS DataBase Reference2687-43-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-20/21/22
Safety Statements 22-24/25-8-36-26
WGK Germany 3
RTECS NC3040000
3
TSCA Yes
HS Code 29280000
MSDS Information
ProviderLanguage
Benzylhydroxylamine hydrochloride English
SigmaAldrich English
ACROS English
ALFA English
O-Benzylhydroxylamine hydrochloride Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
UsesO-Benzylhydroxylamine hydrochloride is a reagent used for the synthesis of hydroxylamines and hydroxyamates.
UsesFor use in the formation of nitrones from carbonyl compounds and their use in cycloaddition reactions. Used as a reagent used in the synthesis of hydroxylamines and hydroxyamates. Effective reagent used to prepare α-hydroxybenzylamines from α-hydroxyketones.
Purification MethodsRecrystallise the hydrochloride from H2O or EtOH. [Beilstein 6 IV 2562.]
6-(PHENYLSULFANYL)IMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE O-(2,6-DICHLOROBENZYL)OXIME O1-[4-(TRIFLUOROMETHYL)BENZOYL]-2-CHLOROETHANEHYDROXIMAMIDE Topotecan hydrochloride Methoxyammonium chloride O2-(4-CHLOROBENZOYL)-3-CHLOROPYRAZINE-2-CARBOHYDROXIMAMIDE N-[(2-CHLOROBENZOYL)OXY]-2-(4,5-DICHLORO-1H-IMIDAZOL-1-YL)ACETAMIDE N'-(4-Chlorobenzoyloxy)-4-nitrobenzimidamide N-[(4-CHLOROBENZOYL)OXY]-2-(4,5-DICHLORO-1H-IMIDAZOL-1-YL)ACETAMIDE O1-(2-CHLOROBENZOYL)-3-[(4,5-DICHLORO-1H-IMIDAZOL-1-YL)METHYL]BENZENE-1-CARBOHYDROXIMAMIDE O2-[3-(TRIFLUOROMETHYL)BENZOYL]-3-CHLOROPYRAZINE-2-CARBOHYDROXIMAMIDE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 2-CHLOROBENZOATE 5-CHLORO-4-(([(2,6-DICHLOROBENZOYL)OXY]IMINO)METHYL)-1,3-DIMETHYL-1H-PYRAZOLE 4-([(BENZOYLOXY)IMINO]METHYL)-1-(4-CHLOROPHENOXY)-2-NITROBENZENE 2-(2-CHLOROETHYL)-4-OXO-3,4-DIHYDRO-2H-1,3-BENZOXAZIN-3-YL 4-CHLOROBENZOATE 6-[(4-CHLOROPHENYL)SULFANYL]IMIDAZO[2,1-B][1,3]THIAZOLE-5-CARBALDEHYDE O-(2,4-DICHLOROBENZYL)OXIME DL-Octopamine hydrochloride 5(6)-CARBOXY-2',7'-DICHLOROFLUORESCEIN DIACETATE N-SUCCINIMIDYL ESTER Cyclohexylamine hydrochloride

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