1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro-

Base Information

Chemical Name:1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro-
CAS No.:88876-88-4
Molecular Formula:C8H12 N4 O3
Molecular Weight:212.208
Hs Code.:2933990090
NSC Number:347503
DSSTox Substance ID:DTXSID301213980
Nikkaji Number:J22.929F
ChEMBL ID:CHEMBL63753
Mol file:88876-88-4.mol

Synonyms:1-(2-nitro-1-imidazolyl)-3-aziridino-2-propanol;NSC 347503;NSC-347503;RSU 1069;RSU-1069

Suppliers and Price of 1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1-(2-NITRO-1-IMIDAZOYL)-3-(1-AZIRIDINYL)-2-PROPANOL 95.00%
5MG
$ 505.44

Total 17 raw suppliers

Chemical Property of 1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro-

Chemical Property:

Vapor Pressure:8.63E-10mmHg at 25°C
Boiling Point:474°C at 760 mmHg
Flash Point:240.5°C
PSA：86.88000
Density:1.59g/cm³
LogP:-0.07110
XLogP3:-0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:212.09094026
Heavy Atom Count:15
Complexity:241

Purity/Quality:

99% ^*data from raw suppliers

1-(2-NITRO-1-IMIDAZOYL)-3-(1-AZIRIDINYL)-2-PROPANOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN1CC(CN2C=CN=C2[N+](=O)[O-])O

Technology Process of 1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro-

There total 4 articles about 1H-Imidazole-1-ethanol, alpha-(1-aziridinylmethyl)-2-nitro- 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:

: 129448-97-1,122178-49-8,153667-41-5,123708-77-0
α-<<(2-bromoethyl)amino>methyl>-2-nitro-1H-imidazole-1-ethanol monohydrobromide

: 88876-88-4
NSC 347503

Guidance literature:: With triethylamine; In various solvent(s); at 25 ℃; for 0.5h;
DOI:10.1021/jm00107a047

Reference yield:

: 129449-06-5
3-<2-hydroxy-3-(2-nitro-1H-imidazol-1-yl)propyl>-2-oxazolidinone

: 88876-88-4
NSC 347503

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / 31percent HBr, HOAc / 20.3 h / Ambient temperature

2: Et₃N / various solvent(s) / 0.5 h / 25 °C

With hydrogen bromide; acetic acid; triethylamine; In various solvent(s);
DOI:10.1021/jm00107a047

Reference yield:

: 21899-19-4
(R,S)-3-(oxiranylmethyl)-2-oxazolidinone

: 88876-88-4
NSC 347503

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Cs₂CO₃ / 1.) EtOH, reflux, 20 min, 2.) reflux, 6 h

2: 54 percent / 31percent HBr, HOAc / 20.3 h / Ambient temperature

3: Et₃N / various solvent(s) / 0.5 h / 25 °C

With hydrogen bromide; caesium carbonate; acetic acid; triethylamine; In various solvent(s);
DOI:10.1021/jm00107a047