1(2H)-Naphthalenone, 3,4-dihydro-, oxime

Base Information

• Chemical Name: 1(2H)-Naphthalenone, 3,4-dihydro-, oxime
• CAS No.: 3349-64-2
• Molecular Formula: C₁₀H₁₁NO
• Molecular Weight: 161.203
• Hs Code.: 2928000090
• European Community (EC) Number: 222-106-8
• ChEMBL ID: CHEMBL3212158
• Mol file: 3349-64-2.mol

Synonyms:3,4-Dihydronaphthalen-1(2H)-one oxime;3349-64-2;tetralone oxime;1,2,3,4-Tetrahydronaphthalen-1-one oxime;(1E)-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE OXIME;68253-36-1;3,4-dihydro-1(2H)-naphthalenone oxime;1(2H)-Naphthalenone, 3,4-dihydro-, oxime;N-[(1Z)-1,2,3,4-tetrahydronaphthalen-1-ylidene]hydroxylamine;MLS000694989;SCHEMBL1204352;CHEMBL3212158;HMS555B14;YFDVQUUMKXZPLK-KHPPLWFESA-N;AMY24819;CCG-44785;MFCD00029228;STK315642;AKOS000305965;DS-2728;NCGC00246550-01;SMR000334858;1(4H)-Naphthalenone, 2,3-dihydro, oxime;(1E)-3,4-Dihydro-1(2H)-naphthalenone oxime;(1Z)-3,4-dihydronaphthalen-1(2H)-one oxime;5M-732;(1E)-3,4-Dihydro-1(2H)-naphthalenone oxime #;(1E)-N-hydroxy-3,4-dihydronaphthalen-1(2H)-imine;SR-01000634601-1;(E)-N-(3,4-dihydro-2H-naphthalen-1-ylidene)-hydroxylamine;N-[(1E)-1,2,3,4-tetrahydronaphthalen-1-ylidene]hydroxylamine

Chemical Property of 1(2H)-Naphthalenone, 3,4-dihydro-, oxime

Chemical Property:

• Vapor Pressure: 0.000149mmHg at 25°C
• Melting Point: 103 °C
• Refractive Index: 1.601
• Boiling Point: 318.6 °C at 760 mmHg
• PKA: 11.46±0.20(Predicted)
• Flash Point: 194.4 °C
• PSA: 32.59000
• Density: 1.16 g/cm³
• LogP: 2.20120
• Storage Temp.: Sealed in dry,Room Temperature
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 161.084063974
• Heavy Atom Count: 12
• Complexity: 188

Purity/Quality:

99% ^*data from raw suppliers

Tetralone-1-Oxime ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2=CC=CC=C2C(=NO)C1
• Isomeric SMILES: C1CC2=CC=CC=C2/C(=N/O)/C1

Technology Process of 1(2H)-Naphthalenone, 3,4-dihydro-, oxime

There total 9 articles about 1(2H)-Naphthalenone, 3,4-dihydro-, 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: 100.0%

3,4-dihydronaphthalene-1(2H)-one (529-34-0) → 1-tetralone oxime (3349-64-2,68253-36-1,100485-58-3)

Guidance literature:

With hydroxylamine hydrochloride;

DOI:10.1021/jo902259u

Reference yield: 100.0%

→ 1-tetralone oxime (3349-64-2,68253-36-1,100485-58-3)

Guidance literature:

Reference yield: 95.0%

5,6,7,8-tetrahydro-8-quinolinone (56826-69-8) → 1-tetralone oxime (3349-64-2,68253-36-1,100485-58-3)

Guidance literature:

With hydroxylamine hydrochloride;

DOI:10.1039/c7ob02126g

upstream raw materials:

3,4-dihydronaphthalene-1(2H)-one

tetralin

1,2-Dihydronaphthalene

1,2,3,4-tetrahydronaphthalen-1-amine

Downstream raw materials:

1-acetamidonaphthalene

1-amino-naphthalene

3,4-dihydro-2H-1-naphthalenone O-tosyloxime

3-(4-methoxy-phenyl)-4,5-dihydro-naphtho[1,2-c]isoxazole