- Substituted phenylureas and phenylamides as vanilloid receptor ligands and their preparation, United States, , ,
Cas no 937843-60-2 ((2-fluoro-4-nitrophenyl)methanamine)
937843-60-2 structure
Product Name:(2-fluoro-4-nitrophenyl)methanamine
CAS No:937843-60-2
MF:C7H7FN2O2
MW:170.141084909439
CID:1000104
PubChem ID:45121148
Update Time:2023-11-28
(2-fluoro-4-nitrophenyl)methanamine Chemical and Physical Properties
Names and Identifiers
-
- Benzenemethanamine, 2-fluoro-4-nitro-
- (2-fluoro-4-nitrophenyl)methanamine
- 2-Fluoro-4-nitrobenzenemethanamine (ACI)
- 2-Fluoro-4-nitrobenzylamine
-
- Inchi: 1S/C7H7FN2O2/c8-7-3-6(10(11)12)2-1-5(7)4-9/h1-3H,4,9H2
- InChI Key: PFNBFQGEYYHVRJ-UHFFFAOYSA-N
- SMILES: [O-][N+](C1C=C(F)C(CN)=CC=1)=O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
(2-fluoro-4-nitrophenyl)methanamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| CHENG DOU FEI BO YI YAO Technology Co., Ltd. | ARK-1826-5g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 95% | 5g |
$347 | 2023-09-07 | |
| Alichem | A012000237-250mg |
2-Fluoro-4-nitrobenzylamine |
937843-60-2 | 97% | 250mg |
$489.60 | 2023-08-31 | |
| Alichem | A012000237-500mg |
2-Fluoro-4-nitrobenzylamine |
937843-60-2 | 97% | 500mg |
$855.75 | 2023-08-31 | |
| Alichem | A012000237-1g |
2-Fluoro-4-nitrobenzylamine |
937843-60-2 | 97% | 1g |
$1490.00 | 2023-08-31 | |
| Enamine | EN300-1850274-1g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 1g |
$160.0 | 2023-09-19 | ||
| Enamine | EN300-1850274-5g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 5g |
$525.0 | 2023-09-19 | ||
| Enamine | EN300-1850274-10g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 10g |
$837.0 | 2023-09-19 | ||
| Enamine | EN300-1850274-0.05g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 0.05g |
$134.0 | 2023-09-19 | ||
| Enamine | EN300-1850274-0.1g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 0.1g |
$141.0 | 2023-09-19 | ||
| Enamine | EN300-1850274-0.25g |
(2-fluoro-4-nitrophenyl)methanamine |
937843-60-2 | 0.25g |
$147.0 | 2023-09-19 |
(2-fluoro-4-nitrophenyl)methanamine Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid Solvents: Tetrahydrofuran ; 6 h, reflux
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid monohydrate Solvents: Tetrahydrofuran ; 6 h, reflux
Reference
- Preparation of methylsulfonamidomethylphenylpryidinylmethylpropanamide derivatives and analogs for use as vanilloid receptor ligands, United States, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid Solvents: Tetrahydrofuran ; 6 h, reflux
Reference
- Substituted pyrazolyl-based carboxamide and urea derivatives bearing a phenyl moiety substituted with an N-containing group as vanilloid receptor ligands and their preparation, World Intellectual Property Organization, , ,
Production Method 4
Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid monohydrate Solvents: Tetrahydrofuran ; 6 h, reflux
Reference
- Preparation of amine substituted methanesulfonamide derivatives as vanilloid receptor ligands, United States, , ,
Production Method 5
Reaction Conditions
1.1 Reagents: Hydrazine hydrate (1:1) Solvents: Tetrahydrofuran ; 6 h, reflux; reflux → rt
1.2 Reagents: Potassium bicarbonate ; pH 12 - 13, rt
1.2 Reagents: Potassium bicarbonate ; pH 12 - 13, rt
Reference
- Preparation of methylsulfonamidomethylphenylpyridinylmethylpropanamide derivatives and analogs for use as vanilloid receptor ligands, United States, , ,
Production Method 6
Reaction Conditions
1.1 Reagents: Benzoyl peroxide , N-Bromosuccinimide Solvents: Carbon tetrachloride ; 15 h, reflux
1.2 Reagents: Potassium phthalimide Solvents: Dimethylformamide ; 15 h, rt
1.3 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid Solvents: Tetrahydrofuran ; 6 h, reflux
1.2 Reagents: Potassium phthalimide Solvents: Dimethylformamide ; 15 h, rt
1.3 Reagents: Hydrazine hydrate (1:1) Catalysts: p-Toluenesulfonic acid Solvents: Tetrahydrofuran ; 6 h, reflux
Reference
- Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic templateAnn, Jihyae; Sun, Wei; Zhou, Xing; Jung, Aeran; Baek, Jisoo; et al, Bioorganic & Medicinal Chemistry Letters, 2016, 26(15), 3603-3607
(2-fluoro-4-nitrophenyl)methanamine Raw materials
(2-fluoro-4-nitrophenyl)methanamine Preparation Products
(2-fluoro-4-nitrophenyl)methanamine Related Literature
-
Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
-
Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
-
Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
-
Christopher J. Harrison,Kyle J. Berean,Enrico Della Gaspera,Jian Zhen Ou,Richard B. Kaner,Kourosh Kalantar-zadeh,Torben Daeneke Nanoscale, 2016,8, 16276-16283
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