34565-32-7 Usage
Description
(±)-Pestalotin, a pyran-2-one metabolite, is produced by Pencillium decumbens. It is known for its role as a gibberellin synergist and plant growth stimulator. (±)-Pestalotin does not directly influence the elongation of rice seedlings, but it acts synergistically to enhance gibberellic acid-induced elongation.
Uses
Used in Plant Growth Regulation:
(±)-Pestalotin is used as a gibberellin synergist for promoting plant growth. It enhances the effects of gibberellic acid, which is a key hormone in plant growth and development, particularly in elongation processes.
Used in Agriculture:
(±)-Pestalotin is used as a plant growth stimulator in the agricultural industry to improve crop yield and quality. By working synergistically with gibberellic acid, it can potentially increase the growth rate and overall productivity of various crops.
Used in Plant Hormone Research:
(±)-Pestalotin is used as a research tool in the study of plant hormones, specifically gibberellins, to better understand their role in plant growth and development. This knowledge can be applied to develop more effective agricultural practices and improve crop management strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 34565-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34565-32:
(7*3)+(6*4)+(5*5)+(4*6)+(3*5)+(2*3)+(1*2)=117
117 % 10 = 7
So 34565-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H18O4/c1-3-4-5-9(12)10-6-8(14-2)7-11(13)15-10/h7,9-10,12H,3-6H2,1-2H3/t9-,10-/m0/s1
34565-32-7Relevant articles and documents
Divergent asymmetric total synthesis of all four pestalotin diastereomers from (R)-glycidol
Moriyama, Mizuki,Nakata, Kohei,Fujiwara, Tetsuya,Tanabe, Yoo
, (2020/01/28)
All four chiral pestalotin diastereomers were synthesized in a straightforward and divergent manner from common (R)-glycidol. Catalytic asymmetric Mukaiyama aldol reactions of readily-available bis(TMSO)diene (Chan’s diene) with (S)-2-benzyloxyhexanal der
High Diastereoselection in the Aldol Reaction of the Bistrimethylsilyl Enol Ether of Methyl Acetoacetate with 2-Benzyloxyhexanal: Synthesis of (-)-Pestalotin
Hagiwara, Hisahiro,Kimura, Katsuhiko,Uda, Hisashi
, p. 693 - 700 (2007/10/02)
Aldol condensation of the bistrimethylsilyl enol ether of methyl acetoacetate, compound 2, with 2-benzyloxyhexanal 3c affords highly selectively (99:1) the syn-aldol adduct 4c in the presence of titanium tetrachloride.The stereocontrolled synthesis of (-)-pestalotin 7 has been achieved.
Highly Diastereoselective Titanium Tetrachloride-mediated Aldol Condensation of the Bistrimethylsilyl Enol Ether of Acetoacetic Ester with 2-Benzyloxyhexanal. A Synthesis of (-)-Pestalotin
Hagiwara, Hisahiro,Kimura, Katsuhiko,Uda, Hisashi
, p. 860 - 861 (2007/10/02)
Titanium tetrachloride-mediated aldol condensation of the bistrimethylsilyl enol ether of methyl acetoacetate (1) with 2-benzyloxyhexanal (3) gives highly selectively (99:1) the syn aldol adduct (5); the stereocontrolled synthesis of (-)-pestalotin (9) ha
