FENCHYL ACETATE

Base Information

• Chemical Name: FENCHYL ACETATE
• CAS No.: 99341-77-2
• Molecular Formula: C12H20 O2
• Molecular Weight: 196.29
• Hs Code.: 2915390090
• Mol file: 99341-77-2.mol

Synonyms:Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, acetate, (1R,2R,4S)- (9CI); Bicyclo[2.2.1]heptan-2-ol,1,3,3-trimethyl-, acetate, (1R-endo)-

Chemical Property of FENCHYL ACETATE

Chemical Property:

• Vapor Pressure: 0.117mmHg at 25°C
• Refractive Index: n20/D 1.456(lit.)
• Boiling Point: 219.8°Cat760mmHg
• Flash Point: 87.4°C
• PSA: 26.30000
• Density: 1g/cm³
• LogP: 2.76430

Purity/Quality:

99% ^*data from raw suppliers

(1R)-(+)-FENCHYL ACETATE 95.00% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of FENCHYL ACETATE

There total 6 articles about FENCHYL ACETATE 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: 90.0%

fenchol (36386-49-9) + acetic acid (64-19-7,77671-22-8) → 1,3,3-trimethylbicyclo<2.2.1>heptan-2-exo-yl acetate (4057-31-2,13851-11-1,56282-46-3,69651-95-2,76109-40-5,99341-77-2,111821-74-0)

Guidance literature:

With sulfuric acid; Heating;

Reference yield:

nitrosyl acetate (5813-49-0) + 2αH-pinan-3α-ylamine (13293-47-5,17371-27-6,35117-55-6,35117-58-9,35117-61-4,35117-66-9,69460-11-3,69460-12-4,74281-72-4) → terpineol (98-55-5,2438-12-2) + 1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate (4057-31-2,13851-11-1,56282-46-3,69651-95-2,76109-40-5,99341-77-2,111821-74-0) + terpinyl acetate (80-26-2) + pinan-2α-ol (473-54-1,4948-28-1,4948-29-2,18492-55-2,23516-36-1,25926-77-6,35408-04-9,35519-42-7,112574-21-7) + 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:

In acetic acid; at 25 ℃;

Reference yield:

acetic acid (64-19-7,77671-22-8) + 2αH-pinan-3α-ylamine (13293-47-5,17371-27-6,35117-55-6,35117-58-9,35117-61-4,35117-66-9,69460-11-3,69460-12-4,74281-72-4) → camphene (79-92-5) + terpineol (98-55-5,2438-12-2) + 1,3,3-trimethylbicyclo<2.2.1>heptan-2-endo-yl acetate (4057-31-2,13851-11-1,56282-46-3,69651-95-2,76109-40-5,99341-77-2,111821-74-0) + 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 sodium nitrite; for 25h;

upstream raw materials:

fenchol

acetic acid

nitrosyl acetate

2αH-pinan-3α-ylamine

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