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Carbamic acid, (5-bromo-4-methyl-2-pyridinyl)-,1,1-dimethylethyl ester, also known as a b-ectythiocarbamate herbicide, is a chemical compound with the formula C11H16BrN2O2. It is used to control a broad spectrum of grasses and broadleaf weeds in various crops and non-crop areas. Carbamic acid, (5-bromo-4-methyl-2-pyridinyl)-,1,1-dimethylethyl ester works by inhibiting the enzyme acetyl CoA carboxylase, which is essential for fatty acid synthesis in plants, ultimately leading to their death. Due to its potential harmful effects if inhaled, swallowed, or if it comes into contact with skin, it is important to handle this chemical with caution.

748812-64-8

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748812-64-8 Usage

Uses

Used in Agricultural Industry:
Carbamic acid, (5-bromo-4-methyl-2-pyridinyl)-,1,1-dimethylethyl ester is used as a herbicide for controlling a broad spectrum of grasses and broadleaf weeds in various crops. It is effective in managing unwanted plant growth, ensuring the healthy development of desired crops.
Used in Non-Crop Areas:
In non-crop areas, Carbamic acid, (5-bromo-4-methyl-2-pyridinyl)-,1,1-dimethylethyl ester is used as a herbicide to control unwanted vegetation, preventing the overgrowth of grasses and broadleaf weeds. This helps maintain the aesthetic and functional aspects of non-crop areas, such as lawns, gardens, and recreational spaces.

Check Digit Verification of cas no

The CAS Registry Mumber 748812-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,8,8,1 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 748812-64:
(8*7)+(7*4)+(6*8)+(5*8)+(4*1)+(3*2)+(2*6)+(1*4)=198
198 % 10 = 8
So 748812-64-8 is a valid CAS Registry Number.

748812-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(5-bromo-4-methylpyridin-2-yl)carbamate

1.2 Other means of identification

Product number -
Other names TERT-BUTYL 5-BROMO-4-METHYLPYRIDIN-2-YLCARBAMATE

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:748812-64-8 SDS

748812-64-8Downstream Products

748812-64-8Relevant academic research and scientific papers

COMPOUNDS AND USES THEREOF

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Page/Page column 233, (2020/10/20)

The present invention features compounds useful in the treatment of neurological disorders and primary brain cancer. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders and primary brain cancer.

COMPOUNDS AND USES THEREOF

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Page/Page column 226, (2019/10/15)

The present invention features compounds useful in the treatment of neurological disorders. The compounds of the invention, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological disorders.

NAPHTHYRIDINES AS INHIBITORS OF HPK1

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Paragraph 0751; 0752, (2018/10/21)

Naphthyridine compounds and their use as inhibitors of HPK1 are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the naphthyridine compounds.

Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P′1 group

Nantermet, Philippe G.,Barrow, James C.,Lindsley, Stacey R.,Young, Marybeth,Mao, Shi-Shan,Carroll, Steven,Bailey, Carolyn,Bosserman, Michele,Colussi, Dennis,McMasters, Daniel R.,Vacca, Joseph P.,Selnick, Harold G.

, p. 2141 - 2145 (2007/10/03)

Structural modifications of the aminopyridine P1 ′ group of imidazole acetic acid based TAFIa inhibitors led to the discovery of the aminocyclopentyl analog 28, a 1nM TAFIa inhibitor with CLT50 functional activity of 14nM but without selectivity against CPB. While not as active, aminobutyl derivative 27 provided an improved 6.7-fold selectivity for TAFIa versus CPB.

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