499769-96-9 Usage
Description
1,3-Benzothiazol-2-ylboronic acid, also known as BZT2B, is a chemical compound with a purity of 97%. It is a member of the boronic acid class of compounds and is widely used in organic synthesis, especially in the pharmaceutical and agrochemical industries. 1,3-BENZOTHIAZOL-2-YLBORONIC ACID,97% serves as a crucial building block in the development of new drugs and biologically active molecules due to its reactivity and capacity to form stable complexes with various organic substrates. Additionally, it functions as a reagent in cross-coupling reactions, which are vital for the formation of carbon-carbon bonds in complex organic molecules. 1,3-Benzothiazol-2-ylboronic acid is a significant asset in the research and development of novel chemical compounds with potential applications in therapy and agriculture.
Uses
Used in Pharmaceutical Industry:
1,3-Benzothiazol-2-ylboronic acid, 97% is used as a building block for the development of new drugs and biologically active molecules. Its reactivity and ability to form stable complexes with a wide range of organic substrates make it an essential component in the synthesis of pharmaceutical compounds.
Used in Agrochemical Industry:
1,3-Benzothiazol-2-ylboronic acid, 97% is used as a key component in the creation of agrochemicals. Its reactivity and compatibility with various organic substrates contribute to the development of effective and innovative agrochemical products.
Used in Organic Synthesis:
1,3-Benzothiazol-2-ylboronic acid, 97% is used as a reagent in cross-coupling reactions. These reactions are crucial for the formation of carbon-carbon bonds, which are essential in creating complex organic molecules with potential applications in various industries.
Used in Research and Development:
1,3-Benzothiazol-2-ylboronic acid, 97% is used as a valuable tool in the research and development of new chemical compounds. Its unique properties and reactivity make it an indispensable component in the discovery and synthesis of novel compounds with potential therapeutic or agricultural applications.
Check Digit Verification of cas no
The CAS Registry Mumber 499769-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,9,7,6 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 499769-96:
(8*4)+(7*9)+(6*9)+(5*7)+(4*6)+(3*9)+(2*9)+(1*6)=259
259 % 10 = 9
So 499769-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H6BNO2S/c10-8(11)7-9-5-3-1-2-4-6(5)12-7/h1-4,10-11H
499769-96-9Relevant articles and documents
C-benzo five-membered heteroaromatic aryl glucoside derivative as well as preparation method and application thereof
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Paragraph 0270; 0271, (2016/10/08)
The invention discloses a C-benzo five-membered heteroaromatic aryl glucoside derivative shown in the general formula (I) (in the description), a preparation method of the derivative or an intermediate of the derivative, as well as application of the derivative. In the general formula (I), R, R1, R2, R3, R4, X and Y are defined in the description. The C-benzo five-membered heteroaromatic aryl glucoside derivative is novel in structure, has quite strong inhibitory activity on SGLT-2, has high selection ratio for SGLT-1 and SGLT-2, and can be used for preparing drugs for treating and preventing diseases relevant to SGLT-2.
Xn:Harmful;
