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(2,3-dichloro-4-[2-dimethylaminomethyl-butyryl]phenoxy)acetic acid is a complex organic compound with the molecular formula C14H18Cl2NO4. It is characterized by the presence of two chlorine atoms at the 2nd and 3rd carbon positions of a phenyl ring, a butyryl group (a four-carbon chain with a carboxylic acid at the end) attached to the 4th position of the phenyl ring, and a dimethylaminomethyl group (a methyl group with an additional methyl group attached to the nitrogen) on the butyryl chain. (2,3-dichloro-4-[2-dimethylaminomethyl-butyryl]phenoxy)acetic acid is known for its herbicidal properties, specifically as a selective post-emergence herbicide used in agriculture to control broadleaf and grassy weeds. It works by inhibiting the enzyme acetohydroxyacid synthase, which is crucial for plant growth, ultimately leading to the death of the weed. The chemical's structure and activity make it a valuable tool in modern weed management strategies.

1160-10-7

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1160-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1160-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,6 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1160-10:
(6*1)+(5*1)+(4*6)+(3*0)+(2*1)+(1*0)=37
37 % 10 = 7
So 1160-10-7 is a valid CAS Registry Number.

1160-10-7Downstream Products

1160-10-7Relevant academic research and scientific papers

Process for the Preparation of Ethacrynic Acid

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, (2018/05/03)

The invention provides an improved process for preparing Ethacrynic acid of formula I, including the steps of: (a) reacting 4-butyryl-2,3-dichloro-phenoxy acetic acid of formula II with dimethylamine or its salt to obtain [2,3-dichloro-4-[2-dimethylaminomethyl butyryl phenoxy acetic acid of formula III or its salt; (b) hydrolysing [2,3-dichloro-4-[2-dimethylaminomethyl butyryl phenoxy acetic acid hydrochloride of formula III obtained in step a) with t-butyl amine to obtain t-butyl amine salt of Ethacrynic acid; (c) acidifying the t-butyl amine salt of Ethacrynic acid formed in step b) to obtain Ethacrynic acid of formula I; and(d) optionally purifying the obtained Ethacrynic acid with a solvent mixture of alkyl acetate and hydrocarbon solvent. The invention also provides crystalline t-butylamine salt of Ethacrynic acid and process thereof. Also provide compound Ethacrynic acid having a purity of greater than or equal to 99% and a composition including the compound.

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