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1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine, also known as DCBPA, is a chemical compound belonging to the class of pyrazole derivatives. It is characterized by its white, crystalline solid appearance and a molecular formula of C10H8Cl2N4. DCBPA has been investigated for its potential as an antimicrobial agent and as a precursor in the synthesis of other organic compounds. It also holds promise in pharmaceuticals, agrochemicals, and materials science, particularly in the development of novel polymers and functional materials. However, due to its potential toxicity and health hazards, it is crucial to exercise caution and follow proper safety protocols when handling this compound.

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  • 895929-56-3 Structure
  • Basic information

    1. Product Name: 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine
    2. Synonyms: 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine;1-[(3,4-dichlorophenyl)methyl]-1H-pyrazol-3-amine
    3. CAS NO:895929-56-3
    4. Molecular Formula: C10H9Cl2N3
    5. Molecular Weight: 242.10456
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 895929-56-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 427.2±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.44±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 3.76±0.10(Predicted)
    10. CAS DataBase Reference: 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine(895929-56-3)
    12. EPA Substance Registry System: 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine(895929-56-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 895929-56-3(Hazardous Substances Data)

895929-56-3 Usage

Uses

Used in Antimicrobial Applications:
1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine is used as an antimicrobial agent for its potential to combat various microorganisms, including bacteria and fungi. Its chemical structure allows it to interfere with essential cellular processes in these organisms, thereby inhibiting their growth and proliferation.
Used in Pharmaceutical Industry:
1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine is used as a building block in the pharmaceutical industry for the synthesis of other organic compounds with potential therapeutic applications. Its unique chemical properties make it a valuable component in the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine is used as a starting material for the development of new pesticides and other agricultural chemicals. Its ability to target specific pests and pathogens can contribute to the creation of more effective and targeted pest control solutions.
Used in Materials Science:
1-(3,4-dichlorobenzyl)-1H-pyrazol-3-amine is used as a component in the field of materials science, particularly in the development of novel polymers and functional materials. Its unique chemical structure can be leveraged to create materials with specific properties, such as enhanced strength, durability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 895929-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,9,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 895929-56:
(8*8)+(7*9)+(6*5)+(5*9)+(4*2)+(3*9)+(2*5)+(1*6)=253
253 % 10 = 3
So 895929-56-3 is a valid CAS Registry Number.

895929-56-3Downstream Products

895929-56-3Relevant articles and documents

Design, synthesis and biological evaluation of spiropyrazolopyridone derivatives as potent dengue virus inhibitors

Chen, Haiying,Shi, Pei-Yong,Xie, Xuping,Xu, Jimin,Xue, Yu,Ye, Na,Zhou, Jia,Zou, Jing

, (2020/04/10)

The effective treatment for dengue virus infection continues to be a challenge. We herein reported our continued SAR exploration on the spiropyrazolopyridone scaffold. Introducing different substituents at the 3?- or 5?-site of the pyrazolopyridone core or moving the benzyl chain to the adjacent nitrogen led to a significant loss of potency on DENV-2. While a narrow range of substitutions were tolerated at the para-position of the phenyl ring, di-substitution on the phenyl ring is beneficial for DENV-2 potency and has variable influences on DENV-3 potency depending on the exact compound. Among these molecules, compounds 22 (JMX0376) with 4-chloro-3-fluorobenzyl and 24 (JMX0395) with 2,4-bis(trifluoromethyl)benzyl showed the most potent and broadest inhibitory activities against DENV-1 to ?3 with nanomolar to low micromolar EC50 values.

Pyrazole glucokinase activators

-

, (2008/06/13)

Disclosed herein are pyrazole glucokinase activators of the formula (I) useful for the treatment of metabolic diseases and disorders, preferably diabetes mellitus.

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