(±)-Pestalotin

Base Information

Chemical Name:(±)-Pestalotin
CAS No.:34565-32-7
Molecular Formula:C₁₁H₁₈O₄
Molecular Weight:214.262
Hs Code.:2932999099
Mol file:34565-32-7.mol

Synonyms:PESTALOTIN;PESTALOTIN (6-HYDROXY-3-METHOXY-2-DECEN-5-OLIDE, ANTIBIOTIC LL-P880 ALPHA);

Suppliers and Price of (±)-Pestalotin

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

TRC
Pestalotin
1000μg
$ 495.00

Cayman Chemical
Pestalotin ≥99%
500μg
$ 219.00

Cayman Chemical
Pestalotin ≥99%
2.5mg
$ 821.00

AK Scientific
Pestalotin
2.5mg
$ 1208.00

Total 5 raw suppliers

Chemical Property of (±)-Pestalotin

Chemical Property:

Vapor Pressure:1.67E-07mmHg at 25°C
Melting Point:76-79 °C(Solv: hexane (110-54-3); benzene (71-43-2))
Boiling Point:384.7°Cat760mmHg
PKA:13.90±0.20(Predicted)
Flash Point:148.2°C
PSA：55.76000
Density:1.1g/cm³
LogP:1.38330

Purity/Quality:

99% ^*data from raw suppliers

Pestalotin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Pestalotin is a pyran-2-one metabolite produced by Pencillium decumbens. Pestalotin is a gibberellin synergist and plant growth stimulator. Pestalotin does not influence elongation of rice seedlings when given alone, but acts synergistically to enhance gibberellic acid-induced elongation. Pestalotin is a pyran-2-one metabolite that can act as a gibberellin synergist.

Technology Process of (±)-Pestalotin

There total 62 articles about (±)-Pestalotin 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: 88.0%

: C₁₈H₂₄O₄

: 34565-32-7
(S)-6-((S)-1-hydroxypentyl)-4-methoxy-5,6-dihydro-2H-pyran-2-one

Guidance literature:: With 20% palladium hydroxide-activated charcoal; hydrogen; In ethyl acetate; at 20 - 25 ℃; for 1h;
DOI:10.3390/molecules25020394

Reference yield: 72.9%

: 90898-48-9
(6S,1'S)-(-)-6-(1'-benzyloxypentyl)-5,6-dihydro-4-methoxypyran-2-one

: 34565-32-7
(S)-6-((S)-1-hydroxypentyl)-4-methoxy-5,6-dihydro-2H-pyran-2-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; at 25 ℃; for 26h; under 760 Torr;

Reference yield: 71.0%

: C₁₈H₂₄O₄

: 34565-32-7,52305-12-1,52305-13-2,52305-14-3,53448-08-1,54656-42-7,54656-43-8,94347-33-8,62015-10-5
(6R, 1'S)-(+)-epipestalotin

Guidance literature:: With 20% palladium hydroxide-activated charcoal; hydrogen; In ethyl acetate; at 20 - 25 ℃; for 1h;
DOI:10.3390/molecules25020394