Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester

Base Information

Chemical Name:Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester
CAS No.:102690-89-1
Molecular Formula:C₁₅H₂₅N₂O₄P
Molecular Weight:328.348
Hs Code.:
DSSTox Substance ID:DTXSID901138267

Synonyms:DTXSID901138267;Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester;102690-89-1

Suppliers and Price of Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:328.15519428
Heavy Atom Count:22
Complexity:320

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)N(C(C)C)P(OC)OCCC1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester

There total 1 articles about Phosphoramidous acid, bis(1-methylethyl)-, methyl 2-(4-nitrophenyl)ethyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 100-27-6
2-(4-nitrophenyl)ethanol

: 86030-43-5
N,N-diisopropylmethylphosphonamidic chloride

: 102690-89-1
4-nitrophenethylmethoxydiisopropylaminophosphine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; 1) 0 deg C, 15 min; 2) room temp., 30 min;
DOI:10.1016/S0040-4039(86)80038-7

Reference yield:

: 102690-89-1
4-nitrophenethylmethoxydiisopropylaminophosphine

: 87007-52-1
C₄₂H₄₇N₄O₁₄P

: 160343-20-4
C₅₁H₅₇N₅O₁₉P₂

Guidance literature:: With 1H-tetrazole; iodine; Yield given. Multistep reaction; 1.) MeCN, room temperature, overnight, 2.) 2,6-lutidine, THF, H₂O, 2 min;
DOI:10.1080/15257779408011881

Reference yield:

: 102690-89-1
4-nitrophenethylmethoxydiisopropylaminophosphine

: 88459-54-5
Acetic acid (2R,3S,5R)-2-{[(2R,3S,5R)-2-hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-methoxy-phosphoryloxymethyl}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

: C₃₂H₄₁N₅O₁₈P₂

Guidance literature:: With 1H-tetrazole; iodine; Yield given. Multistep reaction; 1.) MeCN, room temperature, overnight, 2.) 2,6-lutidine, THF, H₂O, 2 min;
DOI:10.1080/15257779408011881