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CHEMBRDG-BB 4005123, also known as (R)-3-Amino-4-(2-amino-phenoxy)butyric acid, is a chemical compound with the molecular formula C10H14N2O3. It is an important intermediate in the synthesis of pharmaceuticals, as it contains both an amino and a phenoxy group, enabling it to participate in various chemical reactions. It is commonly used in the production of drugs or drug-like molecules due to its potential medicinal properties. Additionally, CHEMBRDG-BB 4005123 has the potential to act as a building block for the development of new pharmaceutical compounds with therapeutic applications.

949034-45-1

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949034-45-1 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 4005123 is used as an intermediate in the synthesis of pharmaceuticals for its ability to participate in various chemical reactions and its potential medicinal properties.
Used in Drug Development:
CHEMBRDG-BB 4005123 is used as a building block for the development of new pharmaceutical compounds with therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 949034-45-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,0,3 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 949034-45:
(8*9)+(7*4)+(6*9)+(5*0)+(4*3)+(3*4)+(2*4)+(1*5)=191
191 % 10 = 1
So 949034-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3/c1-3(9)4-2-5(6(10)11)8-7-4/h2H,1H3,(H,7,8)(H,10,11)

949034-45-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Acetyl-1H-pyrazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-acetyl-1H-pyrazole-3-carboxylic acid

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:949034-45-1 SDS

949034-45-1Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE COMPOUNDS, COMPOSITIONS CONTAINING SAME, AND USE THEREOF

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Paragraph 0243-0244; 0246, (2022/01/12)

The present invention provides substituted pyrazole compounds, compositions containing same, and use thereof. The substituted pyrazole compounds comprise a compound represented by formula (I) or a tautomer, stereoisomer, prodrug, crystalline form, pharmaceutically acceptable salt, hydrate, or solvate thereof. The compound represented by formula (I) can serve as a tissue selective androgen receptor modulator (SARM), particularly serving as a drug for treating prostate cancer and other AR-dependent conditions and diseases in which AR antagonism is desired.

Pyrazoleamide derivative and synthesis method and application

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Paragraph 0048; 0067; 0070, (2022/01/10)

The present invention discloses a pyrazoleamide derivative and a synthetic method and application as an androgen receptor antagonist and the preparation of anti-prostate cancer drugs. The present invention provides a method of synthesizing a pentabasole r

Compound and process for synthesizing 5-acetyl-1H-pyrazole-3-carboxylic acid by using compound

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, (2020/06/02)

The invention belongs to the field of chemical synthesis of substances and discloses a compound, application and a process for synthesizing 5-acetyl-1H-pyrazole-3-carboxylic acid by using the compound. A compound 2, 3-butanedione is used as a starting material to synthesize a compound intermediate III, the compound intermediate III is separated out from the system, the product conversion is promoted, the purification purpose can be achieved through filtration, the conversion rate reaches 95%, and the yield is increased; synthesis of an intermediate IV: by taking the intermediate III and a hydrazine compound as raw materials, the pH of the system is regulated, the yield is increased, and impurity production is reduced; after the reaction is ended, concentrating and filtering are carried out, so that the yield reaches 98%, and the HPLC purity is greater than 98.5%; and through the operation, high-purity V is obtained. The process of the invention is simple and safe, high in yield, suitable for industrialization, beneficial to impurity control and capable of reducing quality risks.

PYRAZOLYL-PYRIMIDINE DERIVATIVES AS KINASE INHIBITORS

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Paragraph 0335-0339, (2014/03/24)

The present invention relates to pyrazolyl-pyrimidine derivatives which modulate the activity of protein kinases and are therefore useful in treating diseases caused by dysregulated protein kinase activity. The present invention also provides methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases utilizing such compounds or the pharmaceutical compositions containing them.

PYRAZOLYL-PYRIMIDINE DERIVATIVES AS KINASE INHIBITORS

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Page/Page column 36-37, (2012/11/06)

The present invention relates to pyrazolyl-pyrimidine derivatives which modulate the activity of protein kinases and are therefore useful in treating diseases caused by dysregulated protein kinase activity. The present invention also provides methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and methods of treating diseases utilizing such compounds or the pharmaceutical compositions containing them.

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