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2-BOC-AMINO-4-BROMOTOLUENE is a chemical compound with the molecular formula C11H14BrNO2. It is a derivative of toluene, featuring a bromine atom substituting one of the hydrogen atoms on the aromatic ring and a BOC (tert-butyloxycarbonyl) protecting group attached to the amino group. 2-BOC-AMINO-4-BROMOTOLUENE is recognized for its versatility in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals, due to its ability to participate in various reactions such as nucleophilic substitution, acylation, and cross-coupling reactions. The BOC protecting group's ease of removal under mild conditions further enhances its utility in organic chemistry.

221538-07-4

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221538-07-4 Usage

Uses

Used in Pharmaceutical Industry:
2-BOC-AMINO-4-BROMOTOLUENE is used as a building block for the synthesis of complex organic compounds in the pharmaceutical industry. Its reactivity and the presence of the BOC protecting group make it an important intermediate for the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, 2-BOC-AMINO-4-BROMOTOLUENE is utilized as a key component in the creation of various agrochemicals. Its versatility in undergoing different types of chemical reactions allows for the synthesis of a wide range of compounds with potential applications in agriculture.
Used in Organic Synthesis:
2-BOC-AMINO-4-BROMOTOLUENE is used as a versatile intermediate in organic synthesis for the preparation of complex organic molecules. Its ability to undergo nucleophilic substitution, acylation, and cross-coupling reactions makes it a valuable tool for chemists in constructing diverse organic compounds.
Used in Research and Development:
In research and development settings, 2-BOC-AMINO-4-BROMOTOLUENE is employed as a model compound to study various chemical reactions and mechanisms. Its unique structure and reactivity provide insights into the behavior of similar compounds and contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 221538-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,1,5,3 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 221538-07:
(8*2)+(7*2)+(6*1)+(5*5)+(4*3)+(3*8)+(2*0)+(1*7)=104
104 % 10 = 4
So 221538-07-4 is a valid CAS Registry Number.

221538-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(5-bromo-2-methylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names T-BUTYL 5-BROMO-2-METHYLPHENYLCARBAMATE

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:221538-07-4 SDS

221538-07-4Relevant academic research and scientific papers

1-PYRAZOLYL, 5-, 6- DISUBSTITUTED INDAZOLE DERIVATIVES AS LRRK2 INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF

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Page/Page column 101; 102, (2020/12/29)

The present invention is directed to substituted certain 1-pyrazolyl, 5-, 6- disubstituted indazole derivatives of Formula (I) and pharmaceutically acceptable salts thereof, wherein R1, R2, and ring A are as defined herein, which are potent inhibitors of LRRK2 kinase and may be useful in the treatment or prevention of diseases in which the LRRK2 kinase is involved, such as Parkinson's Disease and other diseases and disorders described herein. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of diseases, such as Parkinson's disease, in which LRRK-2 kinase is involved.

MK2 INHIBITORS AND USES THEREOF

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Paragraph 001125, (2014/10/03)

The present invention provides compounds, compositions thereof, and methods of using the same.

PHENYL-HETEROARYL AMINE COMPOUNDS AND THEIR USES

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Page/Page column 117, (2012/06/01)

The present invention provides a compound of formula (I): and pharmaceutically acceptable salts, enantiomers, stereoisomers, rotamers, tautomers, diastereomers, or racemates thereof. Also provided are methods of treating a disease or condition mediated by CDK9 using the compounds of Formula I, and pharmaceutical compositions comprising such compounds

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