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6-Hydroxytremetone is a naturally occurring chemical compound found in the venom of certain spiders, specifically the Australian funnel-web spider (Atrax robustus). It is a tremetone, a class of compounds characterized by their complex polyketide structure and diverse biological activities. 6-Hydroxytremetone exhibits neurotoxic properties, which contribute to the venom's ability to paralyze and immobilize its prey. The compound has been studied for its potential applications in understanding the molecular mechanisms of spider venom and its potential use in the development of novel therapeutics. However, due to its complex structure and potential toxicity, further research is needed to fully explore its potential benefits and risks.

6906-88-3

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6906-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6906-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,0 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6906-88:
(6*6)+(5*9)+(4*0)+(3*6)+(2*8)+(1*8)=123
123 % 10 = 3
So 6906-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H14O3/c1-7(2)12-5-9-4-10(8(3)14)11(15)6-13(9)16-12/h4,6,12,15H,1,5H2,2-3H3/t12-/m1/s1

6906-88-3Downstream Products

6906-88-3Relevant academic research and scientific papers

MODIFICATION OF THE NICKL REACTION. A GENERAL SYNTHETIC APPROACH TO 2-VINYL-2,3-DIHYDROBENZOFURANS

Bigi, Franca,Casiraghi, Giovanni,Casnati, Giuseppe,Sartori, Giovanni

, p. 169 - 174 (2007/10/02)

The annelation reaction of metal phenolates 1 with 1,4-dibromo-2-butenes 2 to give 2-vinyl-2,3-dihydrobenzofuran derivatives 3 (Nickl reaction) was critically examined and markedly improved.Use of lithium phenolates, instead of sodium phenolates, as substrates and toluene, instead of methanol, as reaction medium, caused the yield of annelated compounds to rise dramatically.The relevance of this modified route to the synthesis of Euparinoid 2,3-dihydrobenzofurans and their synthetic analogues was emphasized.

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