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Tert-Butyl 4-bromo-2-nitrobenzoate, an organic chemical compound with the formula C11H12BrNO4, is a reactive ester that serves as a building block in organic synthesis. It is a yellow crystalline solid with a high boiling point and is sparingly soluble in water. Known for its use in the preparation of various pharmaceuticals and agrochemicals, tert-Butyl 4-bromo-2-nitrobenzoate should be handled and stored with caution due to its potential hazards, including skin and eye irritation.

890315-72-7

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890315-72-7 Usage

Uses

Used in Pharmaceutical Industry:
Tert-Butyl 4-bromo-2-nitrobenzoate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to facilitate the creation of complex organic molecules. Its reactivity allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, tert-Butyl 4-bromo-2-nitrobenzoate is utilized as a precursor in the production of agrochemicals, contributing to the development of effective pesticides and other crop protection agents.
Used in Organic Synthesis:
Tert-Butyl 4-bromo-2-nitrobenzoate is employed as a versatile building block in organic synthesis, enabling the construction of a wide range of organic compounds for various applications, including the development of new materials and chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 890315-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,3,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 890315-72:
(8*8)+(7*9)+(6*0)+(5*3)+(4*1)+(3*5)+(2*7)+(1*2)=177
177 % 10 = 7
So 890315-72-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H12BrNO4/c1-11(2,3)17-10(14)8-5-4-7(12)6-9(8)13(15)16/h4-6H,1-3H3

890315-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl 4-bromo-2-nitrobenzoate

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-Nitro-Benzoic Acid 1,1-Dimethylethyl Ester

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:890315-72-7 SDS

890315-72-7Relevant articles and documents

Chemically Engineered Porous Molecular Coatings as Reactive Oxygen Species Generators and Reservoirs for Long-Lasting Self-Cleaning Textiles

Bai, Jiaquan,Chen, Zhenxia,Farha, Omar K.,Han, Wendong,Kirlikovali, Kent O.,Li, Peng,Ma, Kaikai,Wang, Chen,Wang, Yao,Xiao, Jisheng,Xu, Tao

supporting information, (2022/01/08)

Wearable personal protective equipment that is decorated with photoactive self-cleaning materials capable of actively neutralizing biological pathogens is in high demand. Here, we developed a series of solution-processable, crystalline porous materials capable of addressing this challenge. Textiles coated with these materials exhibit a broad range of functionalities, including spontaneous reactive oxygen species (ROS) generation upon absorption of daylight, and long-term ROS storage in dark conditions. The ROS generation and storage abilities of these materials can be further improved through chemical engineering of the precursors without altering the three-dimensional assembled superstructures. In comparison with traditional TiO2 or C3N4 self-cleaning materials, the fluorinated molecular coating material HOF-101-F shows a 10- to 60-fold enhancement of ROS generation and 10- to 20-fold greater ROS storage ability. Our results pave the way for further developing self-cleaning textile coatings for the rapid deactivation of highly infectious pathogenic bacteria under both daylight and light-free conditions.

NOVEL ANTHRANILIC ACID DERIVATIVE OR SALT THEREOF

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, (2008/06/13)

An anthranilic acid derivative represented by the general formula (X) [wherein R1 represents hydrogen or a carboxy-protecting group; R2 represents optionally substituted phenyl, a heterocyclic group, etc.; R3 represents op

NOVEL ANTHRANILIC ACID DERIVATIVE OR SALT THEREOF

-

Page/Page column 40-41, (2008/06/13)

The anthranilic acid derivative or the salt thereof represented by the general formula wherein R1 and R2 are hydrogen atom, or the like; R3 is a phenyl, cycloalkyl or bicyclic heterocyclic group which may be substituted, or the like; R4 is a phenyl, cycloalkyl or pyridyl group which may be substituted, or the like; X1 is an alkylene or alkenylene group which may be substituted or a bond; X2 is the general formula -X3-X4- or -X4-X3-, wherein X3 is a sulfur atom, an imino group or a bond, or the like; X4 means an alkylene or alkenylene group which may be substituted or a bond; is useful for a remedy such as rheumatoid arthritis, osteoarthritis and carcinoma, because it shows MMP-13 production inhibitory effect.

NOVEL ANTHRANILIC ACID DERIVATIVE OR SALT THEREOF

-

Page/Page column 56, (2008/06/13)

An anthranilic acid derivative represented by the general formula (X) [wherein R1 represents hydrogen or a carboxy-protecting group; R2 represents optionally substituted phenyl, a heterocyclic group, etc.; R3 represents optionally substituted phenyl, a monocyclic heterocyclic group, etc.; X1 represents carbonyl, etc.; X2 represents optionally substituted alkylene, a bond, etc.; X3 represents oxygen, a bond, etc.; and X4 represents a group represented by the general formula -X5-X6- or -X6-X5- (wherein X5 means oxygen, a bond, etc.; and X6 means optionally substituted alkylene, a bond, etc.)] or a salt of the derivative. The derivative or salt has an MMP-13 production inhibitory activity and is hence useful as a therapeutic agent for articular rheumatisum, osteoarthritis, cancer, etc.

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