5-Amino-1,3-dihydro-2H-benzimidazol-2-one

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CAS:95-23-8
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5-Amino-1,3-dihydro-2H-benzimidazol-2-one manufacturers

5-Amino-1,3-dihydro-2H-benzimidazol-2-one Basic information
Product Name:5-Amino-1,3-dihydro-2H-benzimidazol-2-one
Synonyms:5-AMINO-2-BENZIMIDAZOLINONE;5-AMINO-2-HYDROXYBENZIMIDAZOLE;5-AMINOBENZIMIDAZOLINONE;5-AMINOBENZIMIDAZOLONE;5-AMINO-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE;5-AMINO-1,3-DIHYDRO-BENZOIMIDAZOL-2-ONE;5(6)-AMINOBENZOIMIDAZOLONE;AKOS BBS-00006487
CAS:95-23-8
MF:C7H7N3O
MW:149.15
EINECS:202-401-8
Product Categories:Imidazol&Benzimidazole;Miscellaneous;Benzimidazole Series;BENZIMIDAZOLE;Intermediates of Dyes and Pigments
Mol File:95-23-8.mol
5-Amino-1,3-dihydro-2H-benzimidazol-2-one Structure
5-Amino-1,3-dihydro-2H-benzimidazol-2-one Chemical Properties
Melting point >300 °C
Boiling point 201.4±19.0 °C(Predicted)
density 1.363±0.06 g/cm3(Predicted)
vapor pressure 0.001Pa at 20℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form Powder
pka11.80±0.30(Predicted)
color White to Amber to Dark purple
InChIInChI=1S/C7H7N3O/c8-4-1-2-5-6(3-4)10-7(11)9-5/h1-3H,8H2,(H2,9,10,11)
InChIKeyBCXSVFBDMPSKPT-UHFFFAOYSA-N
SMILESC1(=O)NC2=CC=C(N)C=C2N1
LogP-0.33 at 23℃ and pH6.5-7.5
CAS DataBase Reference95-23-8(CAS DataBase Reference)
EPA Substance Registry System2H-Benzimidazol-2-one, 5-amino-1,3-dihydro- (95-23-8)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36-22
Safety Statements 26-36/37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
5-Amino-1,3-dihydro-2H-benzimidazol-2-one Usage And Synthesis
Chemical PropertiesCrystalline powder
Uses5-Amino-2-hydroxybenzimidazole is an important reagent in the discovery of potent and selective non-nucleotide small molecule inhibitors of CD73
Synthesis
5-NITRO-2-BENZIMIDAZOLINONE

93-84-5

5-Amino-1,3-dihydro-2H-benzimidazol-2-one

95-23-8

Step: 21b Synthesis of 5-amino-1,3-dihydrobenzimidazol-2-one. Pd/C catalyst (140 mg) was added to a mixed solution of methanol and ethyl acetate containing 5-nitro-1,3-dihydrobenzimidazol-2-one (1.4 g, 7.8 mmol) and the hydrogenation reaction was carried out for 6 hours. The progress of the reaction was monitored by thin layer chromatography (TLC, the unfolding agent was a chloroform solution of 10% methanol). After completion of the reaction, the reaction mixture was filtered through a bed of diatomaceous earth and the filtrate was concentrated to give the target product 5-amino-1,3-dihydrobenzimidazol-2-one (1 g, 86% yield).

References[1] Patent: WO2012/59932, 2012, A1. Location in patent: Page/Page column 161-162
[2] Patent: WO2009/42907, 2009, A1. Location in patent: Page/Page column 78-79
[3] Journal of the American Chemical Society, 1958, vol. 80, p. 1662
[4] Patent: WO2012/115479, 2012, A2. Location in patent: Page/Page column 23
[5] Patent: CN104151251, 2017, B. Location in patent: Paragraph 0024
5-Amino-1,3-dihydro-2H-benzimidazol-2-one Preparation Products And Raw materials
Raw materialsUrea-->5-NITRO-2-BENZIMIDAZOLINONE-->o-Phenylenediamine-->Ethyl acetate-->Methanol-->Hydrogen
Preparation Products5-Acetoacetlamino benzimdazolone
Tag:5-Amino-1,3-dihydro-2H-benzimidazol-2-one(95-23-8) Related Product Information
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