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4-methylphenyl chloroacetate, an organic compound derived from chloroacetic acid and 4-methylphenol, is a colorless liquid with a fruity odor. As a chloroester, it features a chlorine atom attached to the carbon atom of the ester group. This chemical is widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, but requires careful handling due to its potential to cause irritation to the skin, eyes, and respiratory system, as well as the need for proper storage and disposal to prevent environmental contamination.

15150-39-7

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15150-39-7 Usage

Uses

Used in Pharmaceutical Industry:
4-methylphenyl chloroacetate is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to be a key component in the development of new drugs, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 4-methylphenyl chloroacetate serves as an essential intermediate in the synthesis of pesticides and other agrochemical products. Its role in creating effective and targeted solutions helps to improve crop protection and contribute to sustainable agriculture practices.
Used as a Hazardous Material in Safety Protocols:
Due to its potential to cause irritation and require specific handling procedures, 4-methylphenyl chloroacetate is used as a reference material in safety protocols and training programs within laboratories and industries. This ensures that personnel are well-equipped to handle and dispose of the chemical safely, minimizing risks to health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 15150-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,5 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15150-39:
(7*1)+(6*5)+(5*1)+(4*5)+(3*0)+(2*3)+(1*9)=77
77 % 10 = 7
So 15150-39-7 is a valid CAS Registry Number.

15150-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl) 2-chloroacetate

1.2 Other means of identification

Product number -
Other names 4-methylphenyl chloroacetate

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:15150-39-7 SDS

15150-39-7Relevant academic research and scientific papers

MODULATORS OF HSD17B13 AND METHODS OF USE THEREOF

-

Paragraph 0645, (2021/01/23)

The disclosure relates to compounds and pharmaceutical compositions capable of modulating the hydroxysteroid 17-beta dehydrogenase (HSD17B) family member proteins including inhibiting the HSD17B member proteins, e.g. HSD17B13. The disclosure further relates to methods of treating liver diseases, disorders, or conditions with the compounds and pharmaceutical compositions disclosed herein, in which the HSD17B family member protein plays a role.

Synthesis and antibacterial activity of 3-benzylamide derivatives as FtsZ inhibitors

Hu, Zhongping,Zhang, Shasha,Zhou, Weicheng,Ma, Xiang,Xiang, Guangya

supporting information, p. 1854 - 1858 (2017/04/04)

The emergence and spread of multidrug-resistant strains of the human pathological bacteria are generating a threat to public health worldwide. In the current study, a series of PC190723 derivatives was synthesized and investigated for their antimicrobial activity. The compounds exhibited good activity against several Gram-positive bacteria as determined by comparison of diameters of the zone of inhibition of test compounds and standard antibiotics. Compound 9 with a fluorine substitution on the phenyl ring showed the best antibacterial activity in the series against M. smegmatis with the zone ratio of 0.62, and against S. aureus with the zone ratio of 0.44. The results from this study indicate that based on the unique 3-methoxybenzamide pharmacophore, compound 9 may represent a promising lead candidate against Gram-positive bacteria that are worthy of further investigation

Chemistry of diazopolycarbonyl compounds: V. Synthesis, structure, and chemical characteristics of aryl diazoacetates

Zalesov,Kataev

, p. 1666 - 1672 (2007/10/03)

Aryl diazoacetates were prepared, and basing on spectral data and quantum-chemical calculations cis-trans isomerism thereof was proved. The reactions of diazoesters with hydrochloric and sulfuric acids, triphenylphosphine, and dinitrogen tetroxide resulted respectively in aryl chloroacetates, bis(aryloxy-carbonylmethyl) sulfates, triphenylphosphoranylidenehydrazones of aryl 2-oxoethanoates, and N-oxides of diaryl 1,2,5-oxadiazole-3,4-dicarboxylates.

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