Cas no 91374-23-1 (N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine)

N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine structure
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

N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Customs Data

  • HS CODE:2921199090
  • Customs Data:

    China Customs Code:

    2921199090

    Overview:

    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
Reference
Novel method of preparing ropinirole - a generic drug against Parkinson's disease
Chmielowiec, Urszula, Przemysl Chemiczny, 2006, 85(5), 347-348

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
Reference
Novel method of preparing ropinirole - a generic drug against Parkinson's disease
Chmielowiec, 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
Reference
4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonist
Gallagher, 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
Reference
Novel method of preparing ropinirole - a generic drug against Parkinson's disease
Chmielowiec, 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
Reference
4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonist
Gallagher, 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
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 inhibitors
Matera, 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
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 inhibitors
Matera, 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
Reference
4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonist
Gallagher, 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
Reference
Novel method of preparing ropinirole - a generic drug against Parkinson's disease
Chmielowiec, 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
Reference
Novel method of preparing ropinirole - a generic drug against Parkinson's disease
Chmielowiec, 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
Reference
4-[2-(Di-n-propylamino)ethyl]-2(3H)-indolone: a prejunctional dopamine receptor agonist
Gallagher, Gregory Jr.; et al, Journal of Medicinal Chemistry, 1985, 28(10), 1533-6

N,N-Dipropyl-2-(2-methyl-3-nitrophenyl)ethylamine Raw materials

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
Audited Supplier Audited Supplier
(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 ($):discuss personally
Recommended suppliers
Suzhou Senfeida Chemical Co., Ltd
(CAS:91374-23-1)N,N-Dipropyl-2-methyl-3-nitrophenylethanamine
sfd19802
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
Email