(E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl acetate

Base Information

Chemical Name:(E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl acetate
CAS No.:94723-93-0
Molecular Formula:C11H12O3
Molecular Weight:192.214
Hs Code.:
European Community (EC) Number:848-176-5
Nikkaji Number:J2.321.506C
ChEMBL ID:CHEMBL3891153

Synonyms:94723-93-0;[4-[(E)-3-hydroxyprop-1-enyl]phenyl] Acetate;(E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl acetate;(E)-4-(3-Hydroxy-1-propen-1-yl)phenylAcetate;(E)-4-(3-Hydroxy-1-propen-1-yl)phenyl Acetate;starbld0007709;trans-p-acetoxycinnamyl alcohol;4-acetoxy-trans-cinnamylalcohol;trans-4-Acetoxycinnamyl alcohol;CHEMBL3891153;SCHEMBL13568242;AC9160;4-(3-hydroxyprop-1-en-1-yl)phenyl acetate;CS-0458171;4-(E)-3'-Hydroxyprop-1'-enylphenyl acetate;EN300-7504370;EN300-7538984;Acetic acid 4-[(E)-3-hydroxy-1-propenyl]phenyl ester;Phenol, 4-(3-hydroxy-1-propenyl)-, 1-acetate, (E)-;Phenol, 4-[(1E)-3-hydroxy-1-propenyl]-, 1-acetate;Z3815658554;4-[(1E)-3-HYDROXYPROP-1-EN-1-YL]PHENYL ACETATE;Phenol, 4-[(1E)-3-hydroxy-1-propen-1-yl]-, 1-acetate

Suppliers and Price of (E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl 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

Total 4 raw suppliers

Chemical Property of (E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl acetate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:192.078644241
Heavy Atom Count:14
Complexity:203

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OC1=CC=C(C=C1)C=CCO
Isomeric SMILES:CC(=O)OC1=CC=C(C=C1)/C=C/CO

Technology Process of (E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl acetate

There total 8 articles about (E)-4-(3-Hydroxyprop-1-en-1-yl)phenyl 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%

: 58505-83-2,157096-53-2
4‐((E)-2-formylvinyl)phenyl acetate

: 94723-93-0
acetic acid (E)-4-(3-hydroxypropenyl)phenyl ester

Guidance literature:: With sodium tetrahydroborate; potassium dihydrogenphosphate; In methanol; at 0 ℃; for 1h;
DOI:10.1055/s-1994-25477

Reference yield: 81.0%

: 33527-94-5
4-acetoxyiodobenzene

: 107-18-6
allyl alcohol

: 94723-93-0
acetic acid (E)-4-(3-hydroxypropenyl)phenyl ester

Guidance literature:: With silver(I) acetate; triphenylphosphine; palladium diacetate; In N,N-dimethyl-formamide; at 70 ℃; for 16h;
DOI:10.1016/j.tet.2006.03.079

Reference yield: 80.0%

: 27542-85-4
4-acetoxycinnamic acid

: 94723-93-0
acetic acid (E)-4-(3-hydroxypropenyl)phenyl ester

Guidance literature:: 4-acetoxycinnamic acid; With chloroformic acid ethyl ester; triethylamine; In 1,4-dioxane; for 1h; Inert atmosphere;

With sodium tetrahydroborate; In 1,4-dioxane; N,N-dimethyl-formamide; for 1h; Inert atmosphere;