2-NP-Amoz

Base Information

• Chemical Name: 2-NP-Amoz
• CAS No.: 183193-59-1
• Molecular Formula: C₁₅H₁₈N₄O₅
• Molecular Weight: 334.332
• European Community (EC) Number: 634-950-8
• DSSTox Substance ID: DTXSID401016484
• Mol file: 183193-59-1.mol

Synonyms:2-NP-AMOZ;183193-59-1;5-(Morpholinomethyl)-3-((2-nitrobenzylidene)amino)oxazolidin-2-one;5-(Morpholinomethyl)-3-(2-nitrobenzylidenamino)-2-oxazolidinone;5-(morpholin-4-ylmethyl)-3-[(E)-(2-nitrophenyl)methylideneamino]-1,3-oxazolidin-2-one;5-[(morpholin-4-yl)methyl]-3-[(E)-[(2-nitrophenyl)methylidene]amino]-1,3-oxazolidin-2-one;5-[(morpholin-4-yl)methyl]-3-{(E)-[(2-nitrophenyl)methylidene]amino}-1,3-oxazolidin-2-one;PCYAMVONOKWOLP-CXUHLZMHSA-N;DTXSID401016484;MFCD04973048;AKOS015855878;AKOS040757078;AS-7043;HY-136456;CS-0129637;2-NP-AMOZ, VETRANAL(TM), analytical standard;J-011723;(E)-5-(morpholinomethyl)-3-((2-nitrobenzylidene)amino)oxazolidin-2-one;2-Nitrobenzaldehyde derivative of 3-Amino-5-morpholino-methyl-1,3-oxazolidone;2-Oxazolidinone, 5-(4-morpholinylmethyl)-3-[[(2-nitrophenyl)methylene]amino]-

Chemical Property of 2-NP-Amoz

Chemical Property:

• PSA: 100.19000
• LogP: 1.48070
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 4
• Exact Mass: 334.12771969
• Heavy Atom Count: 24
• Complexity: 489

Purity/Quality:

97% ^*data from raw suppliers

2-NP-AMOZ ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1COCCN1CC2CN(C(=O)O2)N=CC3=CC=CC=C3[N+](=O)[O-]
• Isomeric SMILES: C1COCCN1CC2CN(C(=O)O2)/N=C/C3=CC=CC=C3[N+](=O)[O-]
• Uses: A derivatized of AMOZ (A634600), a metabolite of Nitrofuran. A derivatized of AMOZ (A634600), a metabolite of Nitrofuran.Environmental contaminants; Food contaminants; Heat processing contaminants

Technology Process of 2-NP-Amoz

There total 1 articles about 2-NP-Amoz 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:

3-amino-5-(morpholinomethyl)oxazolidin-2-one (43056-63-9) + 2-nitro-benzaldehyde (552-89-6) → 3<<(2-Nitrophenyl)methylene>amino>-5-morpholinomethyl-2-oxazolidinone (183193-59-1)

Guidance literature:

With hydrogenchloride; In dimethyl sulfoxide; at 37 ℃; for 20h;

DOI:10.3109/00498259409043272

upstream raw materials:

3-amino-5-(morpholinomethyl)oxazolidin-2-one

2-nitro-benzaldehyde