Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-

Base Information

Chemical Name:Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-
CAS No.:62122-97-8
Molecular Formula:C10H16N2O2
Molecular Weight:
Hs Code.:
NSC Number:295515
DSSTox Substance ID:DTXSID101182258

Synonyms:NSC295515;SCHEMBL19915076;DTXSID101182258;AKOS002665985;AKOS016043620;NSC-295515;Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-;31180-79-7;62122-97-8

Suppliers and Price of Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-

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
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Total 0 raw suppliers

Chemical Property of Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:196.121177757
Heavy Atom Count:14
Complexity:317

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1(C2CCC1(C(=N[N+](=O)[O-])C2)C)C
Isomeric SMILES:CC1(C2CCC1(/C(=N/[N+](=O)[O-])/C2)C)C

Technology Process of Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)-

There total 4 articles about Bicyclo[2.2.1]heptane, 1,7,7-trimethyl-2-(nitroimino)-, (2E)- 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:

: 18674-50-5
camphor oxime

: 31180-79-7,62122-97-8,92935-00-7,114717-12-3
(±)-camphor nitrimine

Guidance literature:: With acetic acid; sodium nitrite; In water; at 20 ℃; for 2h; Inert atmosphere;

Reference yield:

: 76-22-2,68546-28-1
Camphor

: 31180-79-7,62122-97-8,92935-00-7,114717-12-3
(±)-camphor nitrimine

Guidance literature:: Multi-step reaction with 2 steps

1: hydroxylamine hydrochloride; sodium acetate / ethanol / 24 h / 60 °C / Inert atmosphere

2: acetic acid; sodium nitrite / water / 2 h / 20 °C / Inert atmosphere

With hydroxylamine hydrochloride; sodium acetate; acetic acid; sodium nitrite; In ethanol; water;