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Avermectin-A1a is a compound that is part of the Avermectin family, which is a series of drugs and pesticides. It is known for its effectiveness in treating parasitic worms and insect pests, making it a valuable asset in the agricultural and medical industries.

65195-51-9

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65195-51-9 Usage

Uses

Used in Agricultural Industry:
Avermectin-A1a is used as a pesticide for controlling various insect pests. Its application helps in reducing the damage caused by these pests to crops, thereby increasing agricultural productivity and crop yield.
Used in Medical Industry:
Avermectin-A1a is used as an anthelmintic drug for treating parasitic worm infections. It is particularly effective against a range of parasitic worms, including roundworms, whipworms, and filarial worms, which can cause severe health issues in humans and animals. By targeting these parasites, Avermectin-A1a contributes to improved health and well-being for those affected by these infections.

Check Digit Verification of cas no

The CAS Registry Mumber 65195-51-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,9 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65195-51:
(7*6)+(6*5)+(5*1)+(4*9)+(3*5)+(2*5)+(1*1)=139
139 % 10 = 9
So 65195-51-9 is a valid CAS Registry Number.

65195-51-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name avermectin A1a

1.2 Other means of identification

Product number -
Other names doramectin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65195-51-9 SDS

65195-51-9Relevant academic research and scientific papers

SYNTHESIS OF 19-EPI-AVERMECTIN A1a FROM AVERMECTIN B1a

Hanessian, Stephen,Chemla, Philippe

, p. 2719 - 2722 (2007/10/02)

The conversion of avermectin B1a into 19-epi-avermectin A1a was accomplished by an intramolecular Mitsunobu reaction of a Δ2-conjugated seco acid with inversion of configuration, followed by a stereocontrolled deconjugation.

The total synthesis of avermectin A(1a)

Danishefsky,Armistead,Wincott,Selnick,Hungate

, p. 2967 - 2980 (2007/10/02)

Key fragments for the total synthesis of the title compound were elaborated from D-ribose and D-glucose and coupled through a crossed aldol dehydration maneuver (33 + 44→46). An intramolecular variant of the Nozaki reaction (47→48) led to the all-critical

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