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5-amino-4-chloro-2-methylphenyl ethyl carbonate is a chemical compound characterized by the molecular formula C10H12ClNO3. It is an ethyl carbonate derivative featuring a phenyl group that is substituted with an amino group, a chlorine atom, and a methyl group. 5-amino-4-chloro-2-methylphenyl ethyl carbonate plays a significant role in the synthesis of pharmaceuticals and agrochemicals, making it a valuable component in the field of medicinal chemistry for the development of new drugs and pharmaceutical formulations. It also holds potential in the production of pesticides and herbicides, although its chemical properties necessitate careful handling and adherence to safety protocols.

930298-25-2

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930298-25-2 Usage

Uses

Used in Pharmaceutical Industry:
5-amino-4-chloro-2-methylphenyl ethyl carbonate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and formulations. Its unique structure allows for the creation of molecules with specific therapeutic properties, enhancing the range of available treatments.
Used in Agrochemical Industry:
In the agrochemical sector, 5-amino-4-chloro-2-methylphenyl ethyl carbonate is utilized as a precursor in the production of pesticides and herbicides. Its chemical structure can be manipulated to create compounds that effectively control pests and weeds, thereby supporting agricultural productivity and crop protection.
Used in Medicinal Chemistry Research:
5-amino-4-chloro-2-methylphenyl ethyl carbonate serves as a valuable research tool in medicinal chemistry, where it is employed to explore the potential of new drug candidates. Its versatile chemical properties make it suitable for investigating various biological activities and mechanisms of action, contributing to the advancement of pharmaceutical science.
Used in Chemical Synthesis:
As an ethyl carbonate derivative with a substituted phenyl group, 5-amino-4-chloro-2-methylphenyl ethyl carbonate is used in various chemical synthesis processes. Its reactivity and functional groups make it a useful building block for creating a wide array of organic compounds, expanding the scope of synthetic chemistry.
Safety Precautions:
Due to the chemical properties of 5-amino-4-chloro-2-methylphenyl ethyl carbonate, it is essential to handle 5-amino-4-chloro-2-methylphenyl ethyl carbonate with care. Appropriate safety measures, including the use of personal protective equipment, should be taken to minimize potential risks associated with its use in research, pharmaceutical, and agrochemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 930298-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,0,2,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 930298-25:
(8*9)+(7*3)+(6*0)+(5*2)+(4*9)+(3*8)+(2*2)+(1*5)=172
172 % 10 = 2
So 930298-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12ClNO3/c1-3-14-10(13)15-9-5-8(12)7(11)4-6(9)2/h4-5H,3,12H2,1-2H3

930298-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-amino-4-chloro-2-methylphenyl) ethyl carbonate

1.2 Other means of identification

Product number -
Other names 5-amino-4-chloro-2-methylphenylethylcarbonate

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:930298-25-2 SDS

930298-25-2Relevant academic research and scientific papers

PURINE COMPOUNDS AS HSP90 PROTEIN INHIBITORS FOR THE TREATMENT OF CANCER

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Page/Page column 44-45, (2008/06/13)

Compounds of formula (I) are inhibitors of HSP90, and of utility in the treatment of, for example, cancers: wherein ring A is an aryl or heteroaryl ring or ring system; R1 is hydrogen, fluoro, chloro, bromo, or a radical of formula (1A): -X-AIk

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