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(4-BROMOPHENYLTHIO)DIMETHYL-TERT-BUTYLS&, also known as BB-SMTB, is a specific and potent CYP102A1 variant-dependent sortase A ligase substrate. It is a sulfonium salt that has been studied for use in sortase-mediated ligation reactions, which are commonly used in protein engineering and chemical biology applications. BB-SMTB possesses a unique structure and reactivity, making it a valuable tool for the development of new protein conjugates and functionalized biomaterials.

153312-70-0

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153312-70-0 Usage

Uses

Used in Protein Engineering:
BB-SMTB is used as a ligase substrate for sortase-mediated ligation reactions, enabling the efficient labeling of recombinant proteins. This application is crucial for various research and therapeutic purposes, as it allows for the site-specific modification of proteins.
Used in Chemical Biology:
In the field of chemical biology, BB-SMTB serves as a potent tool for the development of new protein conjugates and functionalized biomaterials. Its unique reactivity and structure contribute to the advancement of research in this area.
Used in Research and Development:
BB-SMTB is utilized in research and development for the creation of novel protein conjugates and biomaterials, which can have potential applications in various industries, including pharmaceuticals, diagnostics, and biotechnology.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, BB-SMTB is used as a key component in the development of new drugs and drug delivery systems. Its role in protein engineering and chemical biology can lead to the discovery of innovative therapeutic agents and targeted drug delivery methods.
Used in Diagnostics:
In the diagnostics field, BB-SMTB can be employed for the development of new diagnostic tools and techniques, such as protein-based assays and sensors, which can improve the accuracy and efficiency of disease detection and monitoring.
Used in Biotechnology:
BB-SMTB has potential applications in the biotechnology industry, where it can be used to create novel biomaterials and protein conjugates for various purposes, such as tissue engineering, biocatalysis, and environmental applications.

Check Digit Verification of cas no

The CAS Registry Mumber 153312-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,1 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153312-70:
(8*1)+(7*5)+(6*3)+(5*3)+(4*1)+(3*2)+(2*7)+(1*0)=100
100 % 10 = 0
So 153312-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H19BrSSi/c1-12(2,3)15(4,5)14-11-8-6-10(13)7-9-11/h6-9H,1-5H3

153312-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromophenyl)sulfanyl-tert-butyl-dimethylsilane

1.2 Other means of identification

Product number -
Other names (4-bromophenylsulfanyl)-tert-butyldimethylsilane

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:153312-70-0 SDS

153312-70-0Relevant academic research and scientific papers

Boronated thiophenols: A preparation of 4-mercaptophenylboronic acid and derivatives

Brikh, Abdelghani,Morin, Christophe

, p. 82 - 86 (2007/10/03)

4-Mercaptophenylboronic acid derivatives were prepared by a metallation/boration sequence from S-protected 4-bromothiophenols; the t-butyldimethylsilylthioether was found suitable to allow subsequent regeneration of the mercapto group after boration. The parent compound, 4-mercaptophenylboronic acid, could thus be obtained and was subsequently S-alkylated; 4-boronophenylthioacetic acid was prepared without the need to protect the boronic acid group.

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