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(+/-)-5-epi-strigol is a strigolactone, a type of plant hormone that plays a crucial role in regulating plant growth and development, as well as in the interaction between plants and other organisms such as fungi and parasitic plants. It possesses various biological activities, including stimulating seed germination in parasitic weeds, promoting symbiotic relationships with mycorrhizal fungi, and inhibiting shoot branching. Additionally, it is involved in communication between plants and other soil organisms.

51820-11-2

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51820-11-2 Usage

Uses

Used in Agriculture:
(+/-)-5-epi-strigol is used as a tool for controlling parasitic weeds, helping to manage their growth and spread in agricultural fields.
(+/-)-5-epi-strigol is used as a means to improve the efficiency of nutrient uptake in crops, enhancing their growth and productivity.

Check Digit Verification of cas no

The CAS Registry Mumber 51820-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,2 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51820-11:
(7*5)+(6*1)+(5*8)+(4*2)+(3*0)+(2*1)+(1*1)=92
92 % 10 = 2
So 51820-11-2 is a valid CAS Registry Number.

51820-11-2Downstream Products

51820-11-2Relevant academic research and scientific papers

Routes to derivatives of strigol (the witchweed germination factor) modified in the 5-position

Frischmuth, Katja,Samson, Emmanuelle,Kranz, Angelika,Welzel, Peter,Meuer, Heike,Sheldrick, William S.

, p. 9793 - 9806 (1991)

The title compounds were prepared using nucleophilic substitution in the 5- position of 5b, 6b, 11a, and lib or electrophilic addition to the diene system in 4 as key reactions. Methods for configurational assignment at C-5 and C-2′ are discussed.

Synthesis of all eight stereoisomers of the germination stimulant strigol

Reizelman,Scheren,Nefkens,Zwanenburg

, p. 1944 - 1951 (2007/10/03)

(+)-Strigol is a naturally occurring germination stimulant for the seeds of the parasitic weeds Striga and Orobanche. This paper describes the synthesis of all eight stereoisomers of strigol. The absolute configuration of these stereoisomers has been dedu

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