135681-09-3 Usage
Description
(13R)-5-O-Demethylavermectin A(sub 1a) hydrate is a chemical compound that belongs to the avermectin family, which is commonly used as a pesticide and anthelmintic agent. It is derived from the bacterium Streptomyces avermitilis and is known for its potent insecticidal and antiparasitic properties. The hydrate form of this compound refers to the presence of water molecules within its structure, which can affect its stability and solubility.
Used in Agriculture:
(13R)-5-O-Demethylavermectin A(sub 1a) hydrate is used as a pesticide for controlling a wide range of pests. Its potent insecticidal properties make it a valuable tool in pest management, helping to protect crops and increase agricultural productivity.
Used in Veterinary Medicine:
(13R)-5-O-Demethylavermectin A(sub 1a) hydrate is used as an anthelmintic agent for treating parasitic infections in animals. Its effectiveness in controlling parasites contributes to the overall health and well-being of livestock and pets.
Used in Human Health Applications:
(13R)-5-O-Demethylavermectin A(sub 1a) hydrate is used as an antiparasitic agent for treating various parasitic infections in humans. Its ability to disrupt the nervous system of target organisms makes it a valuable tool in disease control and prevention.
Check Digit Verification of cas no
The CAS Registry Mumber 135681-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,8 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135681-09:
(8*1)+(7*3)+(6*5)+(5*6)+(4*8)+(3*1)+(2*0)+(1*9)=133
133 % 10 = 3
So 135681-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C48H72O14/c1-11-25(2)43-28(5)17-18-47(62-43)23-34-20-33(61-47)16-15-27(4)42(26(3)13-12-14-32-24-55-45-40(49)29(6)19-35(46(51)58-34)48(32,45)52)59-39-22-37(54-10)44(31(8)57-39)60-38-21-36(53-9)41(50)30(7)56-38/h12-15,17,19,25-26,30-31,33-45,49-50,52H,11,16,18,20-24H2,1-10H3/b13-12+,27-15+,32-14+/t25-,26-,30-,31-,33+,34-,35-,36-,37-,38-,39-,40+,41-,42+,43+,44-,45+,47+,48+/m0/s1
135681-09-3Relevant articles and documents
Conversion of avermectin B1 to 19-epi-avermectin B1
Blizzard,Bostrom,Margiatto,Mrozik,Fisher
, p. 2723 - 2726 (2007/10/02)
Avermectin B1 (1) has been converted to 19-epi-avermectin B1 (2) in six steps. Analog 2 retains some bioactivity but is substantially less bioactive than 1.
Studies on the deconjugation-epimerization strategy en route to avermectin B(1a): Problems and solutions
Hanessian,Dube,Hodges
, p. 7063 - 7067 (2007/10/02)
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