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1904-24-1

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1904-24-1 Usage

Description

5-AMINO-3-ETHYL-1H-PYRAZOLE is an organic compound that serves as a crucial intermediate in various chemical and pharmaceutical applications due to its unique molecular structure and reactivity.

Uses

Used in Organic Synthesis:
5-AMINO-3-ETHYL-1H-PYRAZOLE is used as a key intermediate for the synthesis of various organic compounds. Its presence in the molecular structure allows for further functionalization and the creation of a wide range of products.
Used in Pharmaceutical Industry:
5-AMINO-3-ETHYL-1H-PYRAZOLE is used as a building block in the development of new pharmaceuticals. Its unique chemical properties make it a valuable component in the design and synthesis of novel drugs with potential therapeutic applications.
Used in Agrochemicals:
5-AMINO-3-ETHYL-1H-PYRAZOLE is used as a raw material in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness and selectivity, leading to improved agricultural outcomes.
Used in Dye Industry:
5-AMINO-3-ETHYL-1H-PYRAZOLE is used as an intermediate in the synthesis of various dyes and pigments. Its chemical properties contribute to the development of dyes with specific color characteristics and improved performance in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1904-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1904-24:
(6*1)+(5*9)+(4*0)+(3*4)+(2*2)+(1*4)=71
71 % 10 = 1
So 1904-24-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H9N3/c1-2-4-3-5(6)8-7-4/h3H,2H2,1H3,(H3,6,7,8)

1904-24-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H50782)  3-Amino-5-ethyl-1H-pyrazole, 97%   

  • 1904-24-1

  • 250mg

  • 567.0CNY

  • Detail
  • Alfa Aesar

  • (H50782)  3-Amino-5-ethyl-1H-pyrazole, 97%   

  • 1904-24-1

  • 1g

  • 2444.0CNY

  • Detail
  • Aldrich

  • (CDS019625)  5-Amino-3-ethyl-1H-pyrazole  AldrichCPR

  • 1904-24-1

  • CDS019625-100MG

  • 966.42CNY

  • Detail
  • Aldrich

  • (755222)  5-Amino-3-ethyl-1H-pyrazole  

  • 1904-24-1

  • 755222-1G

  • 1,776.06CNY

  • Detail

1904-24-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Amino-5-ethyl-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3-Amino-5-ethylpyrazole

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:1904-24-1 SDS

1904-24-1Relevant articles and documents

Identification of TRD-35 as Potent and Selective DRAK2 Inhibitor

Ali, Imran,Park, Sangjun,Jung, Myoung Eun,Lee, Nari,Bibi, Maimoona,Chae, Chong Hak,Yang, Kyung-Min,Kim, Seong-Jin,Choi, Gildon,Lee, Kwangho

supporting information, p. 567 - 569 (2020/03/23)

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Synthesis of pyrazolopyrimidinones using a “one-pot” approach under microwave irradiation

Kelada, Mark,Walsh, John M. D.,Devine, Robert W.,McArdle, Patrick,Stephens, John C.

supporting information, p. 122 - 1228 (2018/06/13)

A simple one-pot method for the microwave-assisted synthesis of substituted pyrazolo[1,5-a]pyrimidinones, a core scaffold in many bioactive and pharmaceutically relevant compounds, has been established. A variety of substituents was tolerated at the 2 and 5 positions, including functionalized aryls, heterocycles, and alkyl groups.

Pyrazolotriazines as inhibitors of nucleases

-

Paragraph 0122; 0123; 0124; 0125; 0126; 0127; 0128-0133, (2016/01/12)

The invention provides compounds represented by the structural formula (1): wherein R1, R2, R3 and R4 are as defined in the claims. The compounds are inhibitors of nucleases, and are useful in particular in a method of treatment and/or prevention of proliferative diseases, neurodegenerative diseases, and other genomic instability associated diseases.

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