antimony, compound with lutetium (1:1)

Base Information

• Chemical Name: antimony, compound with lutetium (1:1)
• CAS No.: 1203-21-0
• Molecular Formula: C₁₂H₁₈O₂
• Molecular Weight: 194.274
• Mol file: 1203-21-0.mol

Synonyms:antimony, compound with lutetium (1:1)

Chemical Property of antimony, compound with lutetium (1:1)

Chemical Property:

• Boiling Point: 97-98 °C(Press: 9 Torr)
• PSA: 26.30000
• Density: 1.03±0.1 g/cm3(Predicted)
• LogP: 2.54030

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of antimony, compound with lutetium (1:1)

There total 11 articles about antimony, compound with lutetium (1:1) 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:

Pinene (80-56-8,177698-18-9,25766-18-1) + acetic acid (64-19-7,77671-22-8) → 2,6,6-trimethylbicyclo[3.1.1]hept-2-en-4-ol acetate (1203-21-0,19890-04-1,19890-07-4,29135-27-1,39863-91-7,73366-07-1,94669-04-2,33522-69-9) + terpinyl acetate (80-26-2)

Guidance literature:

With oxygen; at 100 ℃; for 4h; under 15001.5 Torr; Inert atmosphere;

DOI:10.1016/j.apcata.2012.05.034

Reference yield:

Pinene (80-56-8,177698-18-9,25766-18-1) + acetic acid (64-19-7,77671-22-8) → 2,6,6-trimethylbicyclo[3.1.1]hept-2-en-4-ol acetate (1203-21-0,19890-04-1,19890-07-4,29135-27-1,39863-91-7,73366-07-1,94669-04-2,33522-69-9) + terpinyl acetate (80-26-2) + isobornyl acetate (76-49-3,125-12-2,5655-61-8,6626-35-3,17283-45-3,20347-65-3,28974-17-6,36386-52-4,71424-71-0,92618-89-8)

Guidance literature:

With oxygen; at 100 ℃; for 6h; under 15001.5 Torr; Inert atmosphere;

DOI:10.1016/j.apcata.2012.05.034

Reference yield:

Pinene (80-56-8,177698-18-9,25766-18-1) + acetic acid (64-19-7,77671-22-8) → 2,6,6-trimethylbicyclo[3.1.1]hept-2-en-4-ol acetate (1203-21-0,19890-04-1,19890-07-4,29135-27-1,39863-91-7,73366-07-1,94669-04-2,33522-69-9) + terpinyl acetate (80-26-2) + isobornyl acetate (76-49-3,125-12-2,5655-61-8,6626-35-3,17283-45-3,20347-65-3,28974-17-6,36386-52-4,71424-71-0,92618-89-8) + limonene. (138-86-3,555-08-8,8022-90-0,9003-73-0,95327-98-3)

Guidance literature:

With oxygen; at 100 ℃; for 10h; under 15001.5 Torr; Inert atmosphere;

DOI:10.1016/j.apcata.2012.05.034

upstream raw materials:

Verbenol

acetic anhydride

Pinene

acetic acid

Downstream raw materials:

trans-Verbenol