| Identification | Back Directory | [Name]
4-HYDRAZINOBENZOIC ACID METHYL ESTER HYDROCHLORIDE | [CAS]
6296-89-5 | [Synonyms]
AURORA 1803 methyl 4-hydrazinobenzoate hydrochloride Methyl 4-hydrazinylbenzoate hydrochloride 4-HYDRAZINOBENZOIC ACID METHYL ESTER HYDROCHLORIDE Benzoic acid, 4-hydrazino-, Methyl ester, Monohydrochloride Benzoic acid,4-hydrazinyl-, methyl ester, hydrochloride (1:1) | [Molecular Formula]
C8H11ClN2O2 | [MDL Number]
MFCD01325154 | [MOL File]
6296-89-5.mol | [Molecular Weight]
202.64 |
| Chemical Properties | Back Directory | [Melting point ]
205-207 °C | [storage temp. ]
Inert atmosphere,Room Temperature | [Appearance]
Off-white to light brown Solid | [InChI]
InChI=1S/C8H10N2O2.ClH/c1-12-8(11)6-2-4-7(10-9)5-3-6;/h2-5,10H,9H2,1H3;1H | [InChIKey]
MXSGRGCOQOKOEH-UHFFFAOYSA-N | [SMILES]
C1(C(=O)OC)C=CC(NN)=CC=1.Cl |
| Hazard Information | Back Directory | [Uses]
Methyl 4-hydrazinylbenzoate HCl | [Synthesis]
General procedure for the synthesis of methyl 4-hydrazinylbenzoate hydrochloride from 2-hydrazinylbenzoic acid: 4M dioxane solution of hydrogen chloride (100 mL, 399.60 mmol) was slowly added to a solution of 2-hydrazinylbenzoic acid (15.2 g, 99.90 mmol) in methanol (200 mL). The reaction mixture was stirred at 90 °C for 5 hours. Upon completion of the reaction, it was cooled to 20 °C and the resulting precipitate was collected by filtration, washed with ether (100 mL) and subsequently dried under vacuum to afford the target product methyl 4-hydrazinobenzoate hydrochloride (16.50 g, 82% yield) as a milky white crystalline solid. Mass spectrometry analysis (ESI-) showed m/z (M-H)- = 165; high performance liquid chromatography (HPLC) retention time was 1.12 min. 1H NMR (400.13 MHz, DMSO-d6) δ 3.81 (3H, s, OCH3), 6.99-7.02 (2H, m, Ar-H), 7.86-7.90 (2H, m, Ar- H), 8.98 (1H, s, NH), 10.47 (3H, s, NH3+). | [References]
[1] Patent: WO2008/99145, 2008, A1. Location in patent: Page/Page column 155-156 [2] Patent: WO2008/99145, 2008, A1. Location in patent: Page/Page column 156 |
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