- High-Valent Iron-Oxo Complexes as Dominant Species to Eliminate Pharmaceuticals and Chloride-Containing Intermediates by the Activation of Peroxymonosulfate Under Visible IrradiationBy Zhu, Zhexin et al, Catalysis Letters, 2020, 150(5), 1355-1367
Cas no 1391124-13-2 (Urea, N,N-bis(2-formylphenyl)-)
1391124-13-2 structure
Product Name:Urea, N,N-bis(2-formylphenyl)-
CAS No:1391124-13-2
MF:C15H12N2O3
MW:268.267383575439
CID:5667637
Update Time:2023-09-11
Urea, N,N-bis(2-formylphenyl)- Chemical and Physical Properties
Names and Identifiers
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- Urea, N,N-bis(2-formylphenyl)-
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- Inchi: 1S/C15H12N2O3/c16-15(20)17(13-7-3-1-5-11(13)9-18)14-8-4-2-6-12(14)10-19/h1-10H,(H2,16,20)
- InChI Key: BJPGZLSFTKFVDV-UHFFFAOYSA-N
- SMILES: N(C1=CC=CC=C1C=O)(C1=CC=CC=C1C=O)C(N)=O
Experimental Properties
- Density: 1.353±0.06 g/cm3(Predicted)
- Boiling Point: 478.7±55.0 °C(Predicted)
- pka: 13.68±0.50(Predicted)
Urea, N,N-bis(2-formylphenyl)- Production Method
Production Method 1
Reaction Conditions
1.1R:Oxone, C:125825-47-0, C:25014-41-9, C:Poly-4-vinylpyridine, S:H2O, rt, pH 7
Reference
Urea, N,N-bis(2-formylphenyl)- Raw materials
Urea, N,N-bis(2-formylphenyl)- Preparation Products
- Malic acid (6915-15-7)
- 1a,10b-dihydro-6H-dibenzo[b,f]oxireno[2,3-d]azepine-6-carboxamide (36507-30-9)
- 9-Oxo-10(9H)-acridinecarboxaldehyde (1177432-69-7)
- acridine-9-carbaldehyde (885-23-4)
- Acridone (578-95-0)
- Citric acid (77-92-9)
- (106680-74-4)
- Urea, N,N-bis(2-formylphenyl)- (1391124-13-2)
- DL-Tartaric acid (526-83-0)
- 11-Keto Oxcarbazepine (537693-29-1)
- 4-Formyl-9-oxo-10(9H)-acridinecarboxamide (1095650-06-8)
Urea, N,N-bis(2-formylphenyl)- Related Literature
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Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
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