Basic information Safety Supplier Related

4,4'-DIACETAMIDODIPHENYLMETHANE

Basic information Safety Supplier Related

4,4'-DIACETAMIDODIPHENYLMETHANE Basic information

Product Name:
4,4'-DIACETAMIDODIPHENYLMETHANE
Synonyms:
  • N-[4-(4-acetamidobenzyl)phenyl]acetamide
  • N-[4-[(4-acetamidophenyl)methyl]phenyl]acetamide
  • N-[4-[(4-acetamidophenyl)methyl]phenyl]ethanamide
  • N,N'-(4,4'-Methylenebis(4,1-phenylene))diacetaMide
  • FH1(BRD-K4477)
  • Acetamide,N,N'-(methylenedi-4,1-phenylene)bis-
  • BRD-K4477
  • N,N′-(Methylenedi-4,1-phenylene)bis-acetamide
CAS:
2719-05-3
MF:
C17H18N2O2
MW:
282.34
Product Categories:
  • Inhibitors
Mol File:
2719-05-3.mol
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4,4'-DIACETAMIDODIPHENYLMETHANE Chemical Properties

Melting point:
227-228 °C
Boiling point:
564.6±43.0 °C(Predicted)
Density 
1.201±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
Soluble in DMSO (up to 30 mg/ml)
form 
solid
pka
14.73±0.70(Predicted)
color 
White
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
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Safety Information

Hazard Codes 
N
Risk Statements 
50/53
Safety Statements 
60-61
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4,4'-DIACETAMIDODIPHENYLMETHANE Usage And Synthesis

Description

FH-1 (2719-05-3) enhances differentiation of induced pluripotent stem cells (iPSC) to hepatocytes. Promotes the maturation of iPSC-derived hepatocytes.

Uses

FH 1 is used as an inducer of cell proliferations (i.e. inducing proliferation and differentiation of stem cells for formation of hepatocytes for treatment of liver disease).

Synthesis

108-24-7

101-77-9

2719-05-3

To a solution of 4,4'-diaminodiphenylmethane (50 mg, 0.25 mmol), pyridine (47 mg, 0.60 mmol) and 4-(dimethylamino)pyridine (1 mg) in dichloromethane (2.5 mL) was added acetic anhydride (56 mg, 0.55 mmol). The reaction mixture was stirred at 0 °C and gradually warmed to 25 °C for 12 hours. Upon completion of the reaction, the mixture was poured into water (10 mL) and extracted with ethyl acetate (50 mL x 2). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. To the residue was added ether (10 mL) and the resulting precipitate was collected by filtration to give N,N'-diacetamidodiphenylmethane (59 mg, 0.21 mmol, 84% yield) as a colorless solid. Melting point: 224-225°C (decomposition).1H NMR (DMSO-d6): δ2.02 (s, 6H), 3.80 (s, 2H), 7.11 (d, J=8.2Hz, 4H), 7.48 (d, J=8.2Hz, 4H), 9.88 (br, 2H).13C NMR (DMSO-d6): δ24.2,40.2 ,119.3,129.0,136.3,137.5,168.3. IR (ATR): 1650 cm-1. MS (EI): m/z 282 (M+). Elemental analysis (C17H18N2O2) Calculated values: C, 72.32; H, 6.43; N, 9.92. Measured values: C, 72.21; H, 6.42; N, 9.91.

storage

+4°C

References

[1] JING SHAN. Identification of small molecules for human hepatocyte expansion and iPS differentiation[J]. Nature chemical biology, 2013, 9 8: 514-520. DOI:10.1038/nchembio.1270

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