Cas no 50699-50-8 (Phenyl (3-Chlorophenyl)carbamate)
Phenyl (3-Chlorophenyl)carbamate is a versatile organic compound featuring a chlorinated phenyl group attached to a carbamate moiety. This compound exhibits unique physical and chemical properties, making it valuable in various applications. Its chlorinated aromatic ring contributes to its stability and reactivity, while the carbamate functionality allows for diverse chemical transformations. This product is suitable for use in pharmaceuticals, agrochemicals, and fine chemicals, offering a promising platform for synthetic modifications.
50699-50-8 structure
Product Name:Phenyl (3-Chlorophenyl)carbamate
CAS No:50699-50-8
MF:C13H10ClNO2
MW:247.677002429962
MDL:MFCD00018424
CID:379902
PubChem ID:232110
Update Time:2025-07-16
Phenyl (3-Chlorophenyl)carbamate Chemical and Physical Properties
Names and Identifiers
-
- Carbamic acid,N-(3-chlorophenyl)-, phenyl ester
- (3-Chlor-phenyl)-carbamidsaeure-phenylester
- < 3-Chlor-phenyl> -carbamidsaeure-phenylester
- 3-Nitrobenzoesaeure-phenylester
- 3-Nitro-benzoesaeure-phenylester
- 3-nitro-benzoic acid phenyl ester
- AC1LJFC5
- CTK0E1606
- m-Nitrobenzoesaeurephenylester
- Oprea1_
- phenyl m-nitrobenzoate
- phenyl N-(3-chlorophenyl) carbamate
- Phenyl-(3-nitro-benzoat)
- Phenyl-N-(m-chlorphenyl)carbamat
- SureCN8566918
- EN300-178847
- phenyl N-(3-chlorophenyl)carbamate
- MFCD00018424
- Phenyl hydrogen (3-chlorophenyl)carbonimidate
- phenyl(3-chlorophenyl)carbamate
- phenyl (3-chlorophenyl)carbamate
- SCHEMBL3983149
- AKOS008917040
- SY161627
- 50699-50-8
- NSC-29155
- ODRCCNDEGWDDGA-UHFFFAOYSA-N
- phenyl 3-chlorophenylcarbamate
- DTXSID80964934
- W16050
- NSC29155
- phenyl N-(3-chlorophenyl)-carbamate
- CS-0047029
- DB-199568
- STL479109
- Phenyl (3-Chlorophenyl)carbamate
-
- MDL: MFCD00018424
- Inchi: 1S/C13H10ClNO2/c14-10-5-4-6-11(9-10)15-13(16)17-12-7-2-1-3-8-12/h1-9H,(H,15,16)
- InChI Key: ODRCCNDEGWDDGA-UHFFFAOYSA-N
- SMILES: ClC1=CC=CC(=C1)NC(=O)OC1C=CC=CC=1
Computed Properties
- Exact Mass: 247.0401
- Monoisotopic Mass: 247.0400063g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 17
- Rotatable Bond Count: 3
- Complexity: 254
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 3.9
- Topological Polar Surface Area: 38.3?2
Experimental Properties
- PSA: 38.33
Phenyl (3-Chlorophenyl)carbamate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P506990-100mg |
Phenyl (3-Chlorophenyl)carbamate |
50699-50-8 | 100mg |
$121.00 | 2023-05-17 | ||
| TRC | P506990-1g |
Phenyl (3-Chlorophenyl)carbamate |
50699-50-8 | 1g |
$ 800.00 | 2023-09-06 | ||
| TRC | P506990-2.5g |
Phenyl (3-Chlorophenyl)carbamate |
50699-50-8 | 2.5g |
$ 1765.00 | 2022-06-03 | ||
| eNovation Chemicals LLC | D773540-500mg |
phenyl N-(3-chlorophenyl)carbamate |
50699-50-8 | 95% | 500mg |
$285 | 2024-06-06 | |
| eNovation Chemicals LLC | D773540-2g |
phenyl N-(3-chlorophenyl)carbamate |
50699-50-8 | 95% | 2g |
$710 | 2024-06-06 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1117669-50mg |
Phenyl (3-chlorophenyl)carbamate |
50699-50-8 | 95+% | 50mg |
¥1454.00 | 2024-05-11 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1117669-100mg |
Phenyl (3-chlorophenyl)carbamate |
50699-50-8 | 95+% | 100mg |
¥2160.00 | 2024-05-11 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1117669-250mg |
Phenyl (3-chlorophenyl)carbamate |
50699-50-8 | 95+% | 250mg |
¥3074.00 | 2024-05-11 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1117669-500mg |
Phenyl (3-chlorophenyl)carbamate |
50699-50-8 | 95+% | 500mg |
¥4860.00 | 2024-05-11 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1117669-1g |
Phenyl (3-chlorophenyl)carbamate |
50699-50-8 | 95+% | 1g |
¥6206.00 | 2024-05-11 |
Phenyl (3-Chlorophenyl)carbamate Related Literature
-
Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
-
Eric Besson,Stéphane Gastaldi,Emily Bloch,Selma Aslan,Hakim Karoui,Olivier Ouari,Micael Hardy Analyst, 2019,144, 4194-4203
-
5. Exclusive enantioselective recognition of glucopyranosides by inherently chiral hemicryptophanes?Olivier Perraud,Alexandre Martinez,Jean-Pierre Dutasta Chem. Commun., 2011,47, 5861-5863
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