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2-(2-chlorophenoxy)-2-methylpropanoyl chloride is a chemical compound with the molecular formula C10H10Cl2O3. It is a colorless to pale yellow liquid with a pungent odor. 2-(2-chlorophenoxy)-2-methylpropanoyl chloride is an important intermediate in the synthesis of various agrochemicals, particularly herbicides. It is used in the production of fluazifop-butyl, a selective post-emergence herbicide for controlling grassy weeds in cereal crops. The compound is synthesized through the reaction of 2-chlorophenol with 2-methylpropanoyl chloride, followed by a chlorination step. Due to its reactivity and potential hazards, it is essential to handle this chemical with proper safety measures and in accordance with relevant regulations.

4878-09-5

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4878-09-5 Usage

Appearance

clear, colorless liquid

Odor

pungent

Usage

intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Versatility

versatile building block in organic chemistry, key starting material for the production of various compounds

Reactivity

ability to undergo substitution reactions, valuable for the production of a wide range of chemical products

Safety

corrosive, can cause irritation to the skin, eyes, and respiratory system (handle with caution)

Check Digit Verification of cas no

The CAS Registry Mumber 4878-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4878-09:
(6*4)+(5*8)+(4*7)+(3*8)+(2*0)+(1*9)=125
125 % 10 = 5
So 4878-09-5 is a valid CAS Registry Number.

4878-09-5Relevant academic research and scientific papers

Pd(II)-catalyzed ortho - Or meta-C-H olefination of phenol derivatives

Dai, Hui-Xiong,Li, Gang,Zhang, Xing-Guo,Stepan, Antonia F.,Yu, Jin-Quan

, p. 7567 - 7571 (2013/06/27)

A combination of weakly coordinating auxiliaries and ligand acceleration allows for the development of both ortho- and meta-selective C-H olefination of phenol derivatives. These reactions demonstrate the feasibility of directing C-H functionalizations when functional groups are distal to target C-H bonds. The meta-C-H functionalization of electron-rich phenol derivatives is unprecedented and orthogonal to previous electrophilic substitution of phenols in terms of regioselectivity. These methods are also applied to functionalize α-phenoxyacetic acids, a fibrate class of drug scaffolds.

Discovery of N-[(1S,2S)-3-(4-chlorophenyl)-2-(3-cyanophenyl)-1- methylpropyl]-2-methyl-2-{[5-(trifluoromethyl)pyridin-2-yl]oxy}propanamide (MK-0364), a novel, acyclic cannabinoid-1 receptor inverse agonist for the treatment of obesity

Lin, Linus S.,Lanza Jr., Thomas J.,Jewell, James P.,Liu, Fing,Shah, Shrenik K.,Qi, Hongbo,Tong, Xinchun,Wang, Junying,Xu, Suoyu S.,Fong, Tung M.,Shen, Chun-Pyn,Lao, Julie,Xiao, Jing Chen,Shearman, Lauren P.,Stribling, D. Sloan,Rosko, Kimberly,Strack, Alison,Marsh, Donald J.,Feng, Yue,Kumar, Sanjeev,Samuel, Koppara,Yin, Wenji,Van Der Ploeg, Lex H. T.,Goulet, Mark T.,Hagmann, William K.

, p. 7584 - 7587 (2007/10/03)

The discovery of novel acyclic amide cannabinoid-1 receptor inverse agonists is described. They are potent, selective, orally bioavailable, and active in rodent models of food intake and body weight reduction. A major focus of the optimization process was to increase in vivo efficacy and to reduce the potential for formation of reactive metabolites. These efforts led to the identification of compound 48 for development as a clinical candidate for the treatment of obesity.

SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES WITH A CHAIN EXTENSION

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Page/Page column 25, (2008/06/13)

The invention relates to substituted cyclohexyl-1,4-diamine derivatives, to a method for their production, to medicaments containing said compounds and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.

TANDEM INTRAMOLECULAR WITTIG AND CLAISEN REARRANGEMENT REACTIONS IN THE THERMOLYSIS OF 2-METHYL-2-PHENOXY-PROPIONYL-CYANOMETHYLENETRIPHENYLPHOSPHORANES: SYNTHESIS OF SUBSTITUTED 2H-1-BENZOPYRANS AND BENZOFURANS

Rehman, H.,Rao, Jampani Madhusudana

, p. 5335 - 5340 (2007/10/02)

The preparation and thermolysis in vacuum of 2-methyl-2-phenoxy-propionyl-cyanomethylenetriphenylphosphorane and derivatives containing methyl-, methoxy- and chloro- substituents in the phenoxy ring is reported.The method merges the preparation of phenyl

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