1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one oxime

Base Information

• Chemical Name: 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one oxime
• CAS No.: 2157-47-3
• Molecular Formula: C10H17NO
• Molecular Weight: 167.251
• NSC Number: 100944,501
• DSSTox Substance ID: DTXSID50421084
• Nikkaji Number: J2.242.654K
• Mol file: 2157-47-3.mol

Synonyms:1,3,3-trimethylbicyclo[2.2.1]heptan-2-one oxime;2157-47-3;1,3-TRIMETHYL-2-NORBORNANONE OXIME;AN-584/40181363;(NZ)-N-(1,3,3-trimethyl-2-bicyclo[2.2.1]heptanylidene)hydroxylamine;Fenchoneoxime;NSC501;2-(hydroxyimino)-1,3,3-trimethylbicyclo[2.2.1]heptane;DTXSID50421084;NSC-501;HMS1667I19;NSC100944;AKOS003242797;NSC-100944

Chemical Property of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one oxime

Chemical Property:

• Vapor Pressure: 0.0109mmHg at 25°C
• Boiling Point: 243°Cat760mmHg
• Flash Point: 136.5°C
• Density: 1.14g/cm³
• XLogP3: 2.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 167.131014166
• Heavy Atom Count: 12
• Complexity: 244

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C2CCC(C2)(C1=NO)C)C
• Isomeric SMILES: CC\1(C2CCC(C2)(/C1=N/O)C)C

Technology Process of 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one oxime

There total 9 articles about 1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one oxime 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: 85.0%

1,3,3-trimethyl-2-norbornanone (1195-79-5,126-21-6) → fenchone oxime (2157-47-3)

Guidance literature:

With hydroxylamine hydrochloride; sodium acetate; In methanol; Heating;

Reference yield: 56.0%

(-)-1,3,3-trimethyl-2-norbornanone (7787-20-4,126-21-6) → (-)-Fenchone oxime (2157-47-3,18674-51-6,25072-89-3,25072-90-6,40514-83-8,74163-80-7,133774-99-9)

Guidance literature:

With sodium hydroxide; hydroxylamine hydrochloride; In ethanol; for 120h; Heating;

Reference yield:

fenchone oxime (2157-47-3) → fenchone oxime (2157-47-3,18674-51-6,25072-89-3,25072-90-6,40514-83-8,74163-80-7,133774-99-9)

Guidance literature:

With diethyl ether; isomer(ic) I;

upstream raw materials:

1,3,3-trimethyl-2-norbornanone

1,3,3-trimethyl-bicyclo[2.2.1]heptane-2-thione

hydroxylamine

fenchone

Downstream raw materials:

fenchone oxime

1,3,3-Trimethyl-bicyclo[2.2.1]heptan-2-one O-(5-chloro-2,4-dinitro-phenyl)-oxime

(1,3,3-trimethyl-bicyclo[2.2.1]hept-2-yl)-amide

1,3,3-trimethyl-2-norbornanone

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