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125772-42-1

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125772-42-1 Usage

General Description

4-Tert-butyl-benzamidine is a chemical compound with the formula C11H17N which appears as a white, crystalline solid. It is classified as an organic compound and is commonly used as a reagent in chemical synthesis. It is a derivative of benzamidine, a potent and selective inhibitor of various serine proteases. The tert-butyl group in this compound provides stability and sterically hinders the molecule, making it useful in a variety of chemical reactions. 4-Tert-butyl-benzamidine is often employed in pharmaceutical research and drug discovery as well as in the synthesis of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 125772-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,7 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125772-42:
(8*1)+(7*2)+(6*5)+(5*7)+(4*7)+(3*2)+(2*4)+(1*2)=131
131 % 10 = 1
So 125772-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h4-7H,1-3H3,(H3,12,13)

125772-42-1SDS

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 4-tert-butylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names 4-tert-Butyl-benzamidine

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:125772-42-1 SDS

125772-42-1Upstream product

125772-42-1Relevant articles and documents

MACROCYCLIC BROAD SPECTRUM ANTIBIOTICS

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Paragraph 00162-00163, (2020/12/11)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. In various embodiments, the compounds act by inhibition of bacterial type 1 signal peptidases SpsB and/or LepB, an essential protein in bacteria. Pharmaceutical compositions and methods for treatment using the compounds described herein are also provided.

Three distinct read-out modes for enzyme activity can operate in a semi-wet supramolecular hydrogel

Tamaru, Shun-Ichi,Kiyonaka, Shigeki,Hamachi, Itaru

, p. 7294 - 7304 (2007/10/03)

Assays of hydrolytic enzyme activity, such as of glycosidases and phosphatase, as well as several proteases, using a semi-wet supramolecular hydrogel array composed of a glycosylated amino acetate are described. It has been demonstrated that the microcavity formed by gel fibrils is suitable to immobilize native enzymes without denaturation under semi-wet conditions, and thus the nanofiber has been rationally used as a sensing domain to monitor enzymatic reactions. By using a fluorogenic substrate, reducing the size of the hydrogel can significantly improve the problem of suppressed diffusion within the gel matrix thus making the hydrogel a promising semi-wet matrix for evaluating enzyme activity. Confocal laser scanning microscopy observa lions have shown that an environmentally sensitive fluorescent probe accumulates in the hydrophobic domain of the gel fiber and emits fluorescence more strongly upon hydrolytic cleavage of the substrate peptides. Not only a simple environmentally sensitive probe but also a FRET (fluorescence resonance energy transfer)-type read-out mode can be devised to analyze the enzymatic hydrolysis-triggered redistribution of the probe between the nano-space and the nanofiber to accomplish a more clearly distinguished enzyme assay. Thus, it is clear that three distinct read-out modes, that is, 1) fluorogenic substrates, 2) substrates bearing an environmentally sensitive probe, or 3) a substrate exhibiting FRET, can operate under the semi-wet hydrogel conditions used in these investigations. In addition, owing to the unique properties of the present supramolecular hydrogel in semi-wet conditions, that is, its phase-segregation properties and dynamics, the supramolecular substrate/enzyme array has successfully been used for high-throughput screening of single and multiple enzymes based on their activity, lysate analysis, and quantitative evaluation of inhibitor potency and selectivity.

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