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Ethanone, 1-(2-chloro-4-fluoro-5-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110322-88-8

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110322-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110322-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,3,2 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110322-88:
(8*1)+(7*1)+(6*0)+(5*3)+(4*2)+(3*2)+(2*8)+(1*8)=68
68 % 10 = 8
So 110322-88-8 is a valid CAS Registry Number.

110322-88-8Relevant academic research and scientific papers

Oxobutanoic acid (-2-olefine acid) acid compound and preparation method thereof, herbicide composition and application thereof, and herbicide

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Paragraph 0203-0204; 0206-0208, (2022/03/27)

The invention relates to the field of herbicides, and discloses an oxobutanoic acid (-2-olefine acid) acid compound and a preparation method thereof, a herbicide composition and application thereof, and a herbicide, the compound has a structure as shown in formula (I). The oxobutane (-2-olefine acid) acid compound provided by the invention has higher herbicidal activity when being used for preventing and controlling weeds.

Inhibitors of viral replication, their process of preparation and their therapeutical uses

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, (2012/11/06)

The present invention relates to compounds, their use in the treatment or the prevention of viral disorders, including HIV.

INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES

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, (2012/11/06)

The present invention relates to compounds, their use in the treatment or the prevention of viral disorders, including HIV.

PROCESS FOR THE PREPARATION OF 6-(PERFLUOROALKYL)URACIL COMPOUNDS FROM CARBAMATE COMPOUNDS

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Page 42, (2010/02/06)

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having structural formula (I) from carbamate compounds having structural formula (II).

Processes and intermediate compounds for the preparation of 2-(N,N-disubstituted) amino-4-(perfluoroalkyl)-1, 3- oxazin-6-one and 6-(perfluoroalkyl) uracil compounds

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, (2008/06/13)

An improved process and intermediate compounds for the preparation of 2-(N,N-disubstituted)amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds having the structural formula I and an improved process for the preparation of 6-(perfluoroalkyl)uracil compound

Herbicidal 3 -heterocyclic substituted benzisothiazole and benzisoxazole compounds

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, (2012/07/31)

There are provided 3-heterocyclic substituted benzisothiazole and benzisoxazole compounds having the structural formula I where Q, X, X1 and Z are defined as in claim 1. Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

Process for the preparation of 6-(perfluoroalkyl) uracil compounds form urea compounds

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, (2008/06/13)

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having the structural formula I from urea compounds having the structural formula II

Process for the preparation of 6-(perfluoroalkyl) uracil compounds from 2-(N,N-disubstituted) amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds

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, (2008/06/13)

An improved process for the preparation of 6-(perfluoroalkyl)uracil compounds having the structural formula I from 2-(N,N-disubstituted)amino-4-(perfluoroalkyl)-1,3-oxazin-6-one compounds having the structural formula II

3-(1,2-benzisothiazol- and isoxazol-5-Y1)-2,4(1H,3H)-pyrimidinedione or thione and 3-(1,2-benzisothiazol- and isoxazol-5-y1)-4(3H)-pyrimidinone or thione herbicidal agents

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, (2008/06/13)

There are provided 3-(1,2-benzisothiazol- and isoxazol-5-yl)-2,4(1H,3H)-pyrimidinedione or thione compounds of formula I and 3-(1,2-benzisothiazol- and isoxazol-5-yl)-4(3H)-pyrimidinone or thione compounds of formula II Further provided are compositions and methods comprising those compounds for the control of undesirable plant species.

Herbicidally active derivatives of N-phenyl-3,4,5,6-tetrahydrophthalimide

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, (2008/06/13)

Novel derivatives of N-phenyl-3,4,5,6-tetrahydrophthalimide of the formula I given below have good pre- and post-emergence, selective-herbicidal properties, and they furthermore regulate and inhibit plant growth. The compounds correspond to the formula I

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