p-(2-Nitropropenyl)anisole

Base Information

Chemical Name:p-(2-Nitropropenyl)anisole
CAS No.:207511-16-8
Molecular Formula:C₁₀H₁₁NO₃
Molecular Weight:193.202
Hs Code.:
European Community (EC) Number:241-381-5
NSC Number:65601
DSSTox Substance ID:DTXSID201245093
Nikkaji Number:J287.019C,J1.947.615D
ChEMBL ID:CHEMBL1996638

Synonyms:p-(2-Nitropropenyl)anisole;Benzene, 1-methoxy-4-(2-nitro-1-propenyl)-;1-methoxy-4-[(Z)-2-nitroprop-1-enyl]benzene;17354-63-1;1-(4-METHOXYPHENYL)-2-NITROPROPENE;37629-51-9;NSC65601;1-(P-METHOXYPHENYL)-2-NITRO-1-PROPENE;CHEMBL1996638;XQGFRDLMKKKSAH-FPLPWBNLSA-N;DTXSID201245093;NSC-65601;AKOS003662903;4-Methoxy-beta-methyl-beta-nitrostyrene;4-Methoxy-.beta.-methyl-.beta.-nitrostyrene;1-[(Z)-2-Nitro-1-propenyl]-4-methoxybenzene;CIS-4-METHOXY-BETA-METHYL-BETA-NITRO-STYRENE;Methyl 4-[(1Z)-2-nitro-1-propenyl]phenyl ether #;1-Methoxy-4-[(1Z)-2-nitro-1-propen-1-yl]benzene;207511-16-8;InChI=1/C10H11NO3/c1-8(11(12)13)7-9-3-5-10(14-2)6-4-9/h3-7H,1-2H3/b8-7

Suppliers and Price of p-(2-Nitropropenyl)anisole

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of p-(2-Nitropropenyl)anisole

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:193.07389321
Heavy Atom Count:14
Complexity:224

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=CC1=CC=C(C=C1)OC)[N+](=O)[O-]
Isomeric SMILES:C/C(=C/C1=CC=C(C=C1)OC)/[N+](=O)[O-]

Technology Process of p-(2-Nitropropenyl)anisole

There total 1 articles about p-(2-Nitropropenyl)anisole 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: 62.0%

: 79-24-3
Nitroethane

: 123-11-5
4-methoxy-benzaldehyde

: 207511-16-8
1-methoxy-4-(2-nitro-1(Z)-propenyl)benzene

Guidance literature:: With N-butylamine; In ethanol; Reflux; Inert atmosphere;
DOI:10.1016/j.ejmech.2013.12.029

Reference yield: 88.0%

: 207511-16-8
1-methoxy-4-(2-nitro-1(Z)-propenyl)benzene

: 52271-41-7
4-methoxyphenylacetone oxime

Guidance literature:: With hydroxylamine hydrochloride; sodium acetate; In 1,4-dioxane; perchloric acid; dichloromethane; for 2h; Ambient temperature;
DOI:10.1246/cl.1983.607

Reference yield: 87.0%

: 207511-16-8
1-methoxy-4-(2-nitro-1(Z)-propenyl)benzene

: 122-84-9
4-methoxybenzyl methyl ketone

Guidance literature:: With formaldehyd; In 1,4-dioxane; perchloric acid; dichloromethane; for 0.333333h; Ambient temperature;
DOI:10.1246/cl.1983.607