alpha-Amyrin acetate

Base Information

Chemical Name:alpha-Amyrin acetate
CAS No.:863-76-3
Molecular Formula:C₃₂H₅₂O₂
Molecular Weight:468.764
Hs Code.:
NSC Number:160881
DSSTox Substance ID:DTXSID401006702
Mol file:863-76-3.mol

Synonyms:alpha-amyrin acetate;amyrin acetate

Suppliers and Price of alpha-Amyrin acetate

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
Packaging
price

ChemScene
α-Amyrinacetate
5mg
$ 550.00

Arctom
alpha-Amyrinacetate ≥98%
5mg
$ 268.00

Total 26 raw suppliers

Chemical Property of alpha-Amyrin acetate

Chemical Property:

Appearance/Colour:white crystalline powder
Vapor Pressure:1.93E-10mmHg at 25°C
Melting Point:241 C
Boiling Point:508°C at 760 mmHg
Flash Point:258°C
PSA：26.30000
Density:1.02g/cm³
LogP:8.59560
XLogP3:9.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:468.396730897
Heavy Atom Count:34
Complexity:885

Purity/Quality:

98% Min ^*data from raw suppliers

α-Amyrinacetate ^*data from reagent suppliers

Safty Information:

Pictogram(s): UN NO.
Hazard Codes:UN NO.

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C

Technology Process of alpha-Amyrin acetate

There total 2 articles about alpha-Amyrin 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:

: 22255-10-3,290299-11-5
(3β)-urs-12-en-3-yl palmitate

: 863-76-3,101915-52-0,22395-84-2
urs-12-en-3β-yl acetate

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄

2: pyridine

With pyridine; lithium aluminium tetrahydride;
DOI:10.1016/0031-9422(80)83096-2

Reference yield:

: 108-24-7
acetic anhydride

: 74994-90-4
22,23-dihydro-22-methylenesqualene-2,3-epoxide

: 863-76-3,101915-52-0,22395-84-2
urs-12-en-3β-yl acetate

: 1616-93-9,33055-28-6,64200-19-7
β-amyrin acetate

: 30-nor-29,29-dimethyl-18β-olean-12-en-3β-yl acetate

Guidance literature:: With pyridine; Tween 80; Mechanism; Product distribution; multistep reaction; enzymic cyclization in vitro by microsomes from Pisum sativum; labeling studies;