3336-40-1 Usage
Uses
Used in Agriculture:
IOXYNIL-METHYL is used as a fungicide for controlling diseases in crops such as barley, wheat, and coffee plants. It functions by inhibiting the growth and development of fungal pathogens, thereby protecting the crops from disease.
This application is crucial for maintaining crop health and productivity, as it helps to prevent yield losses due to fungal infections. The use of IOXYNIL-METHYL as a protective foliar spray is favored for its fast action and long-lasting effects, ensuring a more reliable defense against fungal threats.
However, it is important to note that IOXYNIL-METHYL is considered toxic to aquatic organisms, which underscores the necessity of adhering to recommended usage guidelines and safety precautions to minimize environmental risks. Proper handling and application of this chemical are essential to balance its agricultural benefits with environmental stewardship.
Check Digit Verification of cas no
The CAS Registry Mumber 3336-40-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3336-40:
(6*3)+(5*3)+(4*3)+(3*6)+(2*4)+(1*0)=71
71 % 10 = 1
So 3336-40-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H5I2NO/c1-12-8-6(9)2-5(4-11)3-7(8)10/h2-3H,1H3
3336-40-1Relevant academic research and scientific papers
Preparation of Functionalized Diorganomagnesium Reagents in Toluene via Bromine or Iodine/Magnesium-Exchange Reactions
Desaintjean, Alexandre,Danton, Fanny,Knochel, Paul
supporting information, p. 4461 - 4476 (2021/08/13)
A wide range of polyfunctionalized di(hetero)aryl- and dialkenyl-magnesium reagents are prepared in toluene within 10 to 120 minutes between 78 C and 25 C via an I/Mg- or Br/Mg-exchange reaction using reagents of the general formula R2Mg (R = sBu, Mes). Highly sensitive functional groups, such as triazene or nitro, are tolerated in these exchange reactions, enabling the synthesis of various functionalized (hetero)arene and alkene derivatives after quenching with several electrophiles including allyl bromides, acyl chlorides, aldehydes, ketones, and aryl iodides.
Water-soluble meta-poly(phenylene ethynylene) oligomers with stable helical secondary structure
Nguyen, Ha H.,McAliley, James H.,Bruce, David A.
experimental part, p. 2019 - 2028 (2012/07/13)
Two novel water-soluble meta-poly(phenylene ethynylene) (mPPE) copolymers were synthesized and characterized, each contained ester and amine functional groups attached to exohelix positions on the phenylene rings and one contained methoxy endohelix functi
