1,3-BENZODIOXOL-4-AMINE

1,3-BENZODIOXOL-4-AMINE Suppliers list
Company Name: PharmaBlock Sciences (Nanjing),Inc.  
Tel: 025-86918202 4000255188
Email: sales@pharmablock.com
Company Name: Chembon Pharmaceutical Co., Ltd.  
Tel: 028-84252981 18583719936
Email: sales@chembon.com.cn
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Tel: 13761987713
Email: hxzheng@sunwaypharm.cn
Company Name: Chiba Pharmaceutical Science and technology Co, Ltd.  
Tel: 0531-81313138 13066006660
Email: chibapharm@foxmail.com
Company Name: 9ding chemical ( Shanghai) Limited  
Tel: 4009209199
Email: sales@9dingchem.com

1,3-BENZODIOXOL-4-AMINE manufacturers

1,3-BENZODIOXOL-4-AMINE Basic information
Product Name:1,3-BENZODIOXOL-4-AMINE
Synonyms:1,3-BENZODIOXOL-4-AMINE;2H-1,3-benzodioxol-4-aMine;2,3-Methylenedioxyaniline;Aniline, 2,3-(methylenedioxy)-;benzo[d][1,3]dioxol-4-amine
CAS:1668-84-4
MF:C7H7NO2
MW:137.14
EINECS:
Product Categories:
Mol File:1668-84-4.mol
1,3-BENZODIOXOL-4-AMINE Structure
1,3-BENZODIOXOL-4-AMINE Chemical Properties
Melting point 32-33 °C(Solv: hexane (110-54-3))
Boiling point 100-105 °C(Press: 0.09 Torr)
density 1.332±0.06 g/cm3(Predicted)
storage temp. 2-8°C(protect from light)
form powder
pka4.12±0.20(Predicted)
color Brown
InChIInChI=1S/C7H7NO2/c8-5-2-1-3-6-7(5)10-4-9-6/h1-3H,4,8H2
InChIKeyKQMXPHISFRKBJP-UHFFFAOYSA-N
SMILESO1C2=CC=CC(N)=C2OC1
Safety Information
HS Code 2921490090
MSDS Information
1,3-BENZODIOXOL-4-AMINE Usage And Synthesis
Synthesis
TERT-BUTYL 1,3-BENZODIOXOL-4-YLCARBAMATE

111081-10-8

1,3-BENZODIOXOL-4-AMINE

1668-84-4

The general procedure for the synthesis of 4-amino-1,3-benzodioxole from tert-butyl benzo[d][1,3]dioxol-4-ylcarbamate was as follows: the Boc-protected feedstock G2 (257 mg, 1.08 mmol) was dissolved in a dioxane solution (5.0 mL) of 4 M HCl and stirred for 1 h at room temperature. Upon completion of the reaction, the solvent was removed by evaporation and the residue was diluted with saturated sodium bicarbonate solution (a few milliliters) and 1 M NaOH solution (1 mL), followed by extraction with ethyl acetate (EtOAc, 2×). The organic phases were combined, dried over anhydrous magnesium sulfate (MgSO), filtered and evaporated to dryness to afford the crude product 2,3-methylenedioxypropane G3 (158 mg, 106% yield).

References[1] Patent: WO2004/103996, 2004, A1. Location in patent: Page 50
[2] Journal of Medicinal Chemistry, 2004, vol. 47, # 4, p. 871 - 887
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1991, # 2, p. 259 - 262
[4] Patent: US2004/34046, 2004, A1
[5] Patent: WO2004/4732, 2004, A1. Location in patent: Page/Page column 66
1,3-BENZODIOXOL-4-AMINE Preparation Products And Raw materials
Raw materialsTERT-BUTYL 1,3-BENZODIOXOL-4-YLCARBAMATE-->4-Nitrobenzo[d][1,3]dioxole-->Hydrochloric acid-->1,4-Dioxane
Tag:1,3-BENZODIOXOL-4-AMINE(1668-84-4) Related Product Information
MELICOPINE 1-BENZO[1,3]DIOXOL-4-YL-PIPERAZINE BENZO[1,3]DIOXOL-4-METHYLAMINE 5-(6,7-DIMETHOXY-1,2,3,4-TETRAHYDRO-ISOQUINOLIN-1-YL)-BENZO[1,3]DIOXOL-4-YLAMINE 4-Amino-2,2-difluoro-1,3-benzodioxole 5-BROMO-1,3-BENZODIOXOL-4-AMINE O-NITROPIPERONAL Saracatinib TERT-BUTYL 1,3-BENZODIOXOL-4-YLCARBAMATE 5-CHLORO-1,3-BENZODIOXOL-4-AMINE TERT-BUTYL (5-FLUORO-1,3-BENZODIOXOL-4-YL)CARBAMATE 5-FLUORO-1,3-BENZODIOXOL-4-AMINE 1,3-BENZODIOXOL-4-AMINE TERT-BUTYL (5-BROMO-1,3-BENZODIOXOL-4-YL)CARBAMATE 2,2-Difluoro-8H-1,3-dioxa-8-aza- as-indacene-6,7-dione TERT-BUTYL (5-CHLORO-1,3-BENZODIOXOL-4-YL)CARBAMATE