- Novel method of preparing ropinirole - a generic drug against Parkinson's diseaseChmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348
Cas no 91374-23-1 (N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine)
91374-23-1 structure
Product Name:N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine
CAS No:91374-23-1
MF:C15H24N2O2
MW:264.363264083862
MDL:MFCD09751331
CID:61506
Update Time:2023-11-22
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Chemical and Physical Properties
Names and Identifiers
-
- N-(2-Methyl-3-nitrophenethyl)-N-propylpropan-1-amine
- (R)-(+)-9-(2-Hydroxypropyl)adenine
- BENZENEETHANAMINE, 2-METHYL-3-NITRO-N,N-DIPROPYL
- N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine
- N,N-Dipropyl-2-methyl-3-nitrophenylethanamine
- N-[2-(2-methyl-3-nitrophenyl)ethyl]-N-propylpropan-1-amine
- 2-Methyl-3-nitro-N,N-dipropylbenzeneethanamine (ACI)
-
- MDL: MFCD09751331
- Inchi: 1S/C15H24N2O2/c1-4-10-16(11-5-2)12-9-14-7-6-8-15(13(14)3)17(18)19/h6-8H,4-5,9-12H2,1-3H3
- InChI Key: YTNVHUSMDIAWLT-UHFFFAOYSA-N
- SMILES: [O-][N+](C1C(C)=C(CCN(CCC)CCC)C=CC=1)=O
Computed Properties
- Exact Mass: 264.18400
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 19
- Rotatable Bond Count: 8
- Complexity: 259
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
Experimental Properties
- Density: 1.029
- Boiling Point: 373.812°C at 760 mmHg
- Flash Point: 179.9°C
- Refractive Index: 1.525
- PSA: 49.06000
- LogP: 4.09090
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Security Information
- Signal Word:Warning
- Hazard Statement: H302;H315;H319;H335
- Warning Statement: P261;P305+P351+P338
- Storage Condition:2-8 °C
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Customs Data
- HS CODE:2921199090
- Customs Data:
China Customs Code:
2921199090Overview:
2921199090 Other acyclic monoamines and their derivatives and salts.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| AstaTech | 60184-1/G |
N,N-DIPROPYL-2-METHYL-3-NITROPHENYLETHANAMINE |
91374-23-1 | 96% | 1g |
$52 | 2023-09-16 | |
| AstaTech | 60184-5/G |
N,N-DIPROPYL-2-METHYL-3-NITROPHENYLETHANAMINE |
91374-23-1 | 96% | 5g |
$157 | 2023-09-16 | |
| AstaTech | 60184-25/G |
N,N-DIPROPYL-2-METHYL-3-NITROPHENYLETHANAMINE |
91374-23-1 | 96% | 25g |
$550 | 2023-09-16 | |
| Alichem | A019146315-25g |
N-(2-Methyl-3-nitrophenethyl)-N-propylpropan-1-amine |
91374-23-1 | 95% | 25g |
$555.50 | 2023-08-31 | |
| TRC | D492790-500mg |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 500mg |
$ 64.00 | 2023-09-07 | ||
| TRC | D492790-1g |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 1g |
$ 98.00 | 2023-09-07 | ||
| TRC | D492790-2.5g |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 2.5g |
$ 161.00 | 2023-09-07 | ||
| TRC | D492790-5g |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 5g |
$276.00 | 2023-05-18 | ||
| TRC | D492790-10g |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 10g |
$500.00 | 2023-05-18 | ||
| TRC | D492790-25g |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine |
91374-23-1 | 25g |
$988.00 | 2023-05-18 |
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Thionyl chloride
1.2 -
1.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
1.2 -
1.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Hydrochloric acid Solvents: Water
2.1 Reagents: Thionyl chloride
2.2 -
2.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
2.1 Reagents: Thionyl chloride
2.2 -
2.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- Novel method of preparing ropinirole - a generic drug against Parkinson's diseaseChmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348
Production Method 3
Reaction Conditions
1.1 Reagents: Acetic acid , Toluene Solvents: Water
2.1 Reagents: Thionyl chloride
3.1 Reagents: Borane Solvents: Tetrahydrofuran
2.1 Reagents: Thionyl chloride
3.1 Reagents: Borane Solvents: Tetrahydrofuran
Reference
- 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonistGallagher, Gregory Jr.; et al, Journal of Medicinal Chemistry, 1985, 28(10), 1533-6
Production Method 4
Reaction Conditions
1.1 Reagents: Iodine , Sodium borohydride
2.1 Reagents: Hydrogen bromide
3.1 -
4.1 Reagents: Hydrochloric acid Solvents: Water
5.1 Reagents: Thionyl chloride
5.2 -
5.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
2.1 Reagents: Hydrogen bromide
3.1 -
4.1 Reagents: Hydrochloric acid Solvents: Water
5.1 Reagents: Thionyl chloride
5.2 -
5.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- Novel method of preparing ropinirole - a generic drug against Parkinson's diseaseChmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348
Production Method 5
Reaction Conditions
1.1 Reagents: Thionyl chloride Solvents: Pyridine
2.1 Solvents: Ethanol , Water
3.1 Reagents: Acetic acid , Toluene Solvents: Water
4.1 Reagents: Thionyl chloride
5.1 Reagents: Borane Solvents: Tetrahydrofuran
2.1 Solvents: Ethanol , Water
3.1 Reagents: Acetic acid , Toluene Solvents: Water
4.1 Reagents: Thionyl chloride
5.1 Reagents: Borane Solvents: Tetrahydrofuran
Reference
- 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonistGallagher, Gregory Jr.; et al, Journal of Medicinal Chemistry, 1985, 28(10), 1533-6
Production Method 6
Reaction Conditions
1.1 Reagents: Boron trifluoride , Sodium borohydride Solvents: Tetrahydrofuran ; rt; 2.5 h, reflux
1.2 Reagents: Hydrochloric acid Solvents: Water ; 30 min, reflux
1.2 Reagents: Hydrochloric acid Solvents: Water ; 30 min, reflux
Reference
- Synthesis of 4-[2-(dipropylamino)ethyl]-1,3-dihydro-2H-indol-2-one hydrochloride (ropinirole hydrochloride)Sun, Pinghua; et al, Zhongguo Yiyao Gongye Zazhi, 2007, 38(1), 7-8
Production Method 7
Reaction Conditions
1.1 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- A convenient synthesis of 4-(2-hydroxyethyl)indolin-2-one, a useful intermediate for the preparation of both dopamine receptor agonists and protein kinase inhibitorsMatera, Carlo; et al, Monatshefte fuer Chemie, 2014, 145(7), 1139-1144
Production Method 8
Reaction Conditions
1.1 Reagents: Thionyl chloride
1.2 Reagents: Sodium carbonate Solvents: Toluene , Water
2.1 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
1.2 Reagents: Sodium carbonate Solvents: Toluene , Water
2.1 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- A convenient synthesis of 4-(2-hydroxyethyl)indolin-2-one, a useful intermediate for the preparation of both dopamine receptor agonists and protein kinase inhibitorsMatera, Carlo; et al, Monatshefte fuer Chemie, 2014, 145(7), 1139-1144
Production Method 9
Reaction Conditions
1.1 Reagents: Thionyl chloride
2.1 Reagents: Borane Solvents: Tetrahydrofuran
2.1 Reagents: Borane Solvents: Tetrahydrofuran
Reference
- 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonistGallagher, Gregory Jr.; et al, Journal of Medicinal Chemistry, 1985, 28(10), 1533-6
Production Method 10
Reaction Conditions
1.1 -
2.1 Reagents: Hydrochloric acid Solvents: Water
3.1 Reagents: Thionyl chloride
3.2 -
3.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
2.1 Reagents: Hydrochloric acid Solvents: Water
3.1 Reagents: Thionyl chloride
3.2 -
3.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- Novel method of preparing ropinirole - a generic drug against Parkinson's diseaseChmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348
Production Method 11
Reaction Conditions
1.1 Reagents: Hydrogen bromide
2.1 -
3.1 Reagents: Hydrochloric acid Solvents: Water
4.1 Reagents: Thionyl chloride
4.2 -
4.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
2.1 -
3.1 Reagents: Hydrochloric acid Solvents: Water
4.1 Reagents: Thionyl chloride
4.2 -
4.3 Reagents: (T-4)-Trihydro(tetrahydrofuran)boron
Reference
- Novel method of preparing ropinirole - a generic drug against Parkinson's diseaseChmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348
Production Method 12
Reaction Conditions
1.1 Solvents: Ethanol , Water
2.1 Reagents: Acetic acid , Toluene Solvents: Water
3.1 Reagents: Thionyl chloride
4.1 Reagents: Borane Solvents: Tetrahydrofuran
2.1 Reagents: Acetic acid , Toluene Solvents: Water
3.1 Reagents: Thionyl chloride
4.1 Reagents: Borane Solvents: Tetrahydrofuran
Reference
- 4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonistGallagher, Gregory Jr.; et al, Journal of Medicinal Chemistry, 1985, 28(10), 1533-6
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Raw materials
- 2-(2-methyl-3-nitrophenyl)acetic acid
- 2-(3-Nitrophenyl)-N,N-dipropylpropanamide
- 2-Methyl-3-nitrobenzyl alcohol
- 2-(2-methyl-3-nitrophenyl)acetonitrile
- 2-Methyl-3-nitrobenzyl chloride
- 2-Methyl-3-nitrobenzoic acid
- 3-Nitro-2-methyl-benzylbromide
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Preparation Products
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Suppliers
Suzhou Senfeida Chemical Co., Ltd
Gold Member
(CAS:91374-23-1)N,N-Dipropyl-2-methyl-3-nitrophenylethanamine
Order Number:sfd19802
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:38
Price ($):discuss personally
Email:[email protected]
N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Related Literature
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1. An investigation of the electrochemical delithiation process of carbon coated α-Fe2O3nanoparticlesAdrian Brandt,Florian Winter,Sebastian Klamor,Frank Berkemeier,Jatinkumar Rana,Rainer P?ttgen,Andrea Balducci J. Mater. Chem. A, 2013,1, 11229-11236
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M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
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Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
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Recommended suppliers
Suzhou Senfeida Chemical Co., Ltd
(CAS:91374-23-1)N,N-Dipropyl-2-methyl-3-nitrophenylethanamine
Purity:99.9%
Quantity:200kg
Price ($):Inquiry