1219-99-4,MFCD00018541
Catalog No.:AA009DU9

1219-99-4 | N,N'-BIS(P-CHLOROPHENYL)UREA

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$11.00   $8.00
- +
1g
98%
in stock  
$39.00   $27.00
- +
5g
98%
in stock  
$121.00   $85.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA009DU9
Chemical Name:
N,N'-BIS(P-CHLOROPHENYL)UREA
CAS Number:
1219-99-4
Molecular Formula:
C13H10Cl2N2O
Molecular Weight:
281.1373
MDL Number:
MFCD00018541
SMILES:
O=C(Nc1ccc(cc1)Cl)Nc1ccc(cc1)Cl
NSC Number:
12979
Properties
Computed Properties
 
Complexity:
246  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.3  

Downstream Synthesis Route

[1]Pfeifer,Lukas;Engle,KearyM.;Pidgeon,GeorgeW.;Sparkes,HazelA.;Thompson,AmberL.;Brown,JohnM.;Gouverneur,Véronique[JournaloftheAmericanChemicalSociety,2016,vol.138,#40,p.13314-13325]

[2]Catalano,Alessia;Iacopetta,Domenico;Rosato,Antonio;Salvagno,Lara;Ceramella,Jessica;Longo,Francesca;Sinicropi,MariaStefania;Franchini,Carlo[Antibiotics,2021,vol.10,#2,p.1-13]

[3]Beaveretal.[JournaloftheAmericanChemicalSociety,1957,vol.79,p.1236,1242][JournalofOrganicChemistry,1959,vol.24,p.1676]

[4]Andreani,Aldo;Rambaldi,Mirella;Carloni,Patricia;Greci,Lucedio;Stipa,Pierluigi[JournalofHeterocyclicChemistry,1989,vol.26,p.525-529]

[5]Miyahara;Kamiya;Nakadate[ChemicalandPharmaceuticalBulletin,1983,vol.31,#1,p.41-44]

[6]Muccioli,GiulioG.;Wouters,Johan;Charlier,Caroline;Scriba,GerhardK.E.;Pizza,Teresa;DiPace,Pierluigi;DeMartino,Paolo;Poppitz,Wolfgang;Poupaert,JacquesH.;Lambert,DidierM.[JournalofMedicinalChemistry,2006,vol.49,#3,p.872-882]

[7]CurrentPatentAssignee:DUKEUNIVERSITY-WO2020/123675,2020,A1Locationinpatent:Paragraph0181

[1]Pasha;Jayashankara[SyntheticCommunications,2006,vol.36,#12,p.1787-1793]

[2]Locationinpatent:experimentalpartPasha;MadhusudanaReddy[SyntheticCommunications,2009,vol.39,#16,p.2928-2934]

[3]Li,Zheng[SyntheticCommunications,2005,vol.35,#17,p.2325-2331]

[4]Rekunge,DeelipS.;Khatri,ChetanK.;Chaturbhuj,GaneshU.[TetrahedronLetters,2017,vol.58,#45,p.4304-4307]

[5]Kothandapani,Jagatheeswaran;Ganesan,Asaithampi;Ganesan,SubramaniapillaiSelva[Synthesis,2017,vol.49,#3,p.685-692]

[6]Mojtahedi,MohammadM.;Saidi,MohammadR.;Bolourtchian,Mohammad[JournalofChemicalResearch-PartS,1999,#12,p.710-711]

[7]Chattaway;Orton[ChemischeBerichte,1901,vol.34,p.1080]

[8]Bognaretal.[ActaChimicaAcademiaeScientiarumHungaricae,1954,vol.4,p.355,356,362]

[9]Chimishkyan,A.L.;Svetlova,L.P.;Leonova,T.V.;Gluyaev,N.D.[JournalofgeneralchemistryoftheUSSR,1984,vol.54,#7,p.1317-1320][ZhurnalObshcheiKhimii,1984,vol.54,#7,p.1477-1481]

[1]JournaloftheChemicalSociety,1908,vol.93,p.1055,1057

[1]ActaChimicaAcademiaeScientiarumHungaricae,1954,vol.4,p.369,370,377

[1]Rosnati[GazzettaChimicaItaliana,1956,vol.86,p.275,279]

[2]CurrentPatentAssignee:DOWINC-US4275215,1981,A

Literature

Title: Simultaneous determination of triclosan, triclocarban, and transformation products of triclocarban in aqueous samples using solid-phase micro-extraction-HPLC-MS/MS.

Journal: Journal of separation science 20121001

Title: In vitro glucuronidation of the antibacterial triclocarban and its oxidative metabolites.

Journal: Drug metabolism and disposition: the biological fate of chemicals 20120101

Title: Bioaccumulation of triclocarban in Lumbriculus variegatus.

Journal: Environmental toxicology and chemistry 20091201

Title: N,N'-Bis(4-chloro-phen-yl)urea.

Journal: Acta crystallographica. Section E, Structure reports online 20080501

Title: Detection of triclocarban and two co-contaminating chlorocarbanilides in US aquatic environments using isotope dilution liquid chromatography tandem mass spectrometry.

Journal: Environmental research 20070101

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:1219-99-4 Molecular Formula|1219-99-4 MDL|1219-99-4 SMILES|1219-99-4 N,N'-BIS(P-CHLOROPHENYL)UREA
Catalog No.: AA009DU9
1219-99-4,MFCD00018541
1219-99-4 | N,N'-BIS(P-CHLOROPHENYL)UREA
Pack Size: 250mg
Purity: 98%
in stock
$11.00 $8.00
Pack Size: 1g
Purity: 98%
in stock
$39.00 $27.00
Pack Size: 5g
Purity: 98%
in stock
$121.00 $85.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA009DU9
Chemical Name: N,N'-BIS(P-CHLOROPHENYL)UREA
CAS Number: 1219-99-4
Molecular Formula: C13H10Cl2N2O
Molecular Weight: 281.1373
MDL Number: MFCD00018541
SMILES: O=C(Nc1ccc(cc1)Cl)Nc1ccc(cc1)Cl
NSC Number: 12979
Properties
Complexity: 246  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.3  
Downstream Synthesis Route
104-12-1    106-47-8    1219-99-4 

[1]Pfeifer,Lukas;Engle,KearyM.;Pidgeon,GeorgeW.;Sparkes,HazelA.;Thompson,AmberL.;Brown,JohnM.;Gouverneur,Véronique[JournaloftheAmericanChemicalSociety,2016,vol.138,#40,p.13314-13325]

[2]Catalano,Alessia;Iacopetta,Domenico;Rosato,Antonio;Salvagno,Lara;Ceramella,Jessica;Longo,Francesca;Sinicropi,MariaStefania;Franchini,Carlo[Antibiotics,2021,vol.10,#2,p.1-13]

[3]Beaveretal.[JournaloftheAmericanChemicalSociety,1957,vol.79,p.1236,1242][JournalofOrganicChemistry,1959,vol.24,p.1676]

[4]Andreani,Aldo;Rambaldi,Mirella;Carloni,Patricia;Greci,Lucedio;Stipa,Pierluigi[JournalofHeterocyclicChemistry,1989,vol.26,p.525-529]

[5]Miyahara;Kamiya;Nakadate[ChemicalandPharmaceuticalBulletin,1983,vol.31,#1,p.41-44]

[6]Muccioli,GiulioG.;Wouters,Johan;Charlier,Caroline;Scriba,GerhardK.E.;Pizza,Teresa;DiPace,Pierluigi;DeMartino,Paolo;Poppitz,Wolfgang;Poupaert,JacquesH.;Lambert,DidierM.[JournalofMedicinalChemistry,2006,vol.49,#3,p.872-882]

[7]CurrentPatentAssignee:DUKEUNIVERSITY-WO2020/123675,2020,A1Locationinpatent:Paragraph0181

106-47-8    57-13-6    1219-99-4 

[1]Pasha;Jayashankara[SyntheticCommunications,2006,vol.36,#12,p.1787-1793]

[2]Locationinpatent:experimentalpartPasha;MadhusudanaReddy[SyntheticCommunications,2009,vol.39,#16,p.2928-2934]

[3]Li,Zheng[SyntheticCommunications,2005,vol.35,#17,p.2325-2331]

[4]Rekunge,DeelipS.;Khatri,ChetanK.;Chaturbhuj,GaneshU.[TetrahedronLetters,2017,vol.58,#45,p.4304-4307]

[5]Kothandapani,Jagatheeswaran;Ganesan,Asaithampi;Ganesan,SubramaniapillaiSelva[Synthesis,2017,vol.49,#3,p.685-692]

[6]Mojtahedi,MohammadM.;Saidi,MohammadR.;Bolourtchian,Mohammad[JournalofChemicalResearch-PartS,1999,#12,p.710-711]

[7]Chattaway;Orton[ChemischeBerichte,1901,vol.34,p.1080]

[8]Bognaretal.[ActaChimicaAcademiaeScientiarumHungaricae,1954,vol.4,p.355,356,362]

[9]Chimishkyan,A.L.;Svetlova,L.P.;Leonova,T.V.;Gluyaev,N.D.[JournalofgeneralchemistryoftheUSSR,1984,vol.54,#7,p.1317-1320][ZhurnalObshcheiKhimii,1984,vol.54,#7,p.1477-1481]

106-47-8    140-38-5    1219-99-4 

[1]JournaloftheChemicalSociety,1908,vol.93,p.1055,1057

57-13-6    1219-99-4    140-38-5 

[1]ActaChimicaAcademiaeScientiarumHungaricae,1954,vol.4,p.369,370,377

1219-99-4    19950-87-9 

[1]Rosnati[GazzettaChimicaItaliana,1956,vol.86,p.275,279]

[2]CurrentPatentAssignee:DOWINC-US4275215,1981,A

Literature fold

Title: Simultaneous determination of triclosan, triclocarban, and transformation products of triclocarban in aqueous samples using solid-phase micro-extraction-HPLC-MS/MS.

Journal: Journal of separation science20121001

Title: In vitro glucuronidation of the antibacterial triclocarban and its oxidative metabolites.

Journal: Drug metabolism and disposition: the biological fate of chemicals20120101

Title: Bioaccumulation of triclocarban in Lumbriculus variegatus.

Journal: Environmental toxicology and chemistry20091201

Title: N,N'-Bis(4-chloro-phen-yl)urea.

Journal: Acta crystallographica. Section E, Structure reports online20080501

Title: Detection of triclocarban and two co-contaminating chlorocarbanilides in US aquatic environments using isotope dilution liquid chromatography tandem mass spectrometry.

Journal: Environmental research20070101

Building Blocks More >
137125-92-9
137125-92-9
Olivetol-d9
AA009DZ8 | MFCD28899304
1330173-19-7
1330173-19-7
rac N-DeMethyl ProMethazine
AA009E64 | MFCD28899383
137862-78-3
137862-78-3
Isoleucine Valsartan
AA009EE9
133908-85-7
133908-85-7
L-Ribonic acid-1,4-lactone
AA009EOC | MFCD15145094
1246819-24-8
1246819-24-8
Glycidyl Palmitate-d31
AA009EVD | MFCD29036951
1333981-84-2
1333981-84-2
Chloro[(R,R)-N-[2-[2-(4-methylbenzyloxy)ethyl]amino-1,2-diphenylethyl]-p-toluenesulfonamide]ruthenium(II)
AA009F2N | MFCD20922902
13027-26-4
13027-26-4
δ-Tocopherol Acetate
AA009FA7 | MFCD30474441
134-90-7
134-90-7
L-(+)-Threo-chloramphenicol
AA009FGY | MFCD01733852
14158-66-8
14158-66-8
cis-CloMiphene Hydrochloride
AA009FP4 | MFCD08060093
1330750-49-6
1330750-49-6
(3R,4R)-rel-4-(Pyridin-2-yl)pyrrolidine-3-carboxylic acid dihydrochloride
AA009G4H | MFCD06659316
Submit
© 2017 AA BLOCKS, INC. All rights reserved.