[(1R)-1-(Nitromethyl)heptyl]benzene

Base Information

Chemical Name:[(1R)-1-(Nitromethyl)heptyl]benzene
CAS No.:1437326-35-6
Molecular Formula:C₁₄H₂₁NO₂
Molecular Weight:235.326
Hs Code.:
DSSTox Substance ID:DTXSID301293126

Synonyms:[(1R)-1-(Nitromethyl)heptyl]benzene;DTXSID301293126;1437326-35-6

Suppliers and Price of [(1R)-1-(Nitromethyl)heptyl]benzene

Supply Marketing:

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

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Chemical Property of [(1R)-1-(Nitromethyl)heptyl]benzene

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:235.157228913
Heavy Atom Count:17
Complexity:207

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCC(C[N+](=O)[O-])C1=CC=CC=C1
Isomeric SMILES:CCCCCC[C@@H](C[N+](=O)[O-])C1=CC=CC=C1

Technology Process of [(1R)-1-(Nitromethyl)heptyl]benzene

There total 2 articles about [(1R)-1-(Nitromethyl)heptyl]benzene 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: 97.0%

: 119880-60-3
(E)-α-n-hexyl-β-nitrostyrene

: 1437326-35-6
(R)-2-phenyl-1-nitrooctane

Guidance literature:: With C₆₂H₅₆F₆IrN₁₀O₄S₂⁽¹⁺⁾*C₃₂H₁₂BF₂₄^(1-); di-tert-butyl 1,4-dihydro-2,6-dimethyl-3,5-pyridine-dicarboxylate; In toluene; at 20 ℃; for 36h; Temperature; Concentration; Reagent/catalyst; Solvent; Time; enantioselective reaction; Catalytic behavior; Kinetics; Inert atmosphere;
DOI:10.1021/jacs.6b02769

Reference yield:

: 119880-60-3
(E)-α-n-hexyl-β-nitrostyrene

: (S)-2-phenyl-1-nitrooctane

: 1437326-35-6
(R)-2-phenyl-1-nitrooctane

Guidance literature:: With C₃₆H₂₈IrN₆O₄⁽¹⁺⁾*C₃₂H₁₂BF₂₄^(1-); di-tert-butyl 1,4-dihydro-2,6-dimethyl-3,5-pyridine-dicarboxylate; In toluene; at 20 ℃; for 22h; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ja403777k