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4-(4,4,5,5-tetramethyl -1,3,2-dioxaborolan-2-yl)naphthalen-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2043962-01-0

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2043962-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2043962-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,0,4,3,9,6 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2043962-01:
(9*2)+(8*0)+(7*4)+(6*3)+(5*9)+(4*6)+(3*2)+(2*0)+(1*1)=140
140 % 10 = 0
So 2043962-01-0 is a valid CAS Registry Number.

2043962-01-0Downstream Products

2043962-01-0Relevant articles and documents

QUINAZOLINE COMPOUNDS, PREPARATION METHODS AND USES THEREOF

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Paragraph 175, (2022/01/12)

Provided herein are novel compounds, for example, compounds having a Formula (I), Formula (II), or Formula (III), or a pharmaceutically acceptable salt thereof. Also provided herein are methods of preparing the compounds and methods of using the compounds, for example, in inhibiting KRAS G12D in a cancer cell, and/or in treating various cancer such as pancreatic cancer, colorectal cancer, lung cancer or endometrial cancer.

ORGANIC ELECTROLUMINESCENT COMPOUND, ORGANIC ELECTROLUMINESCENT MATERIAL COMPRISING THE SAME, AND ORGANIC ELECTROLUMINESCENT DEVICE

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Paragraph 0108-0110, (2021/06/26)

The present disclosure relates to an organic electroluminescent compound, an organic electroluminescent material, and an organic electroluminescent device comprising the same. The organic electroluminescent compound of the present disclosure can provide a

A COMPOUND HAVING INHIBITORY ACTIVITY AGAINST KRAS G12D MUTATION

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Paragraph 0298-0299, (2021/06/04)

The present invention relates to a compound having inhibitory activity against KRAS G12D mutation or a salt thereof, and relates to a pharmaceutical composition comprising the compound as an active ingredient.

MODULATORS OF PROTEOLYSIS AND ASSOCIATED METHODS OF USE

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, (2019/10/29)

The present disclosure relates to bifunctional compounds, which find utility as modulators of Kirsten rat sarcoma protein (target protein). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hippel-Lindau, cereblon, Inhibitors of Apotosis Proteins or mouse double-minute homolog 2 ligand which binds to the respective E3 ubiquitin ligase and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation, accumulation, and/or overactivation of the target protein are treated or prevented with compounds and compositions of the present disclosure.

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