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5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4) is a chemical compound with the molecular formula C7H12N2, featuring a pyrazole ring and functional groups of isopropyl and methyl. It is soluble in water and has a melting point of 75-77°C. Commonly used as a pharmaceutical intermediate, this compound also exhibits insecticidal properties. Formulated as a hydrochloride salt, it indicates its potential for use in pharmaceutical and agricultural applications.
Used in Pharmaceutical Industry:
5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4) is used as a pharmaceutical intermediate for its ability to be incorporated into the synthesis of various drugs, leveraging its chemical properties to contribute to the development of new medicinal compounds.
Used in Agricultural Industry:
5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4) is used as an insecticide for its insecticidal properties, providing a means to control pests in crops and contribute to effective agricultural practices.

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  • 132558-01-1 Structure
  • Basic information

    1. Product Name: 5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4)
    2. Synonyms: 5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4);3-isopropyl-5-methyl-1H-pyrazole;3-methyl-5-propan-2-yl-2H-pyrazole;5-methyl-3-propan-2-yl-1H-pyrazole
    3. CAS NO:132558-01-1
    4. Molecular Formula: C7H12N2
    5. Molecular Weight: 124.18358
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132558-01-1.mol
  • Chemical Properties

    1. Melting Point: 58-59 °C
    2. Boiling Point: 124-126 °C(Press: 14 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.975±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.88±0.10(Predicted)
    10. CAS DataBase Reference: 5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4)(132558-01-1)
    12. EPA Substance Registry System: 5-isopropyl-3-methyl-1H-pyrazole(SALTDATA: 1.15HCl 0.07N2H4)(132558-01-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132558-01-1(Hazardous Substances Data)

132558-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132558-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,5 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132558-01:
(8*1)+(7*3)+(6*2)+(5*5)+(4*5)+(3*8)+(2*0)+(1*1)=111
111 % 10 = 1
So 132558-01-1 is a valid CAS Registry Number.

132558-01-1Downstream Products

132558-01-1Relevant articles and documents

Study of the reactivity of α-acylenaminoketones. Synthesis of pyrazoles

Negri,Kascheres

, p. 109 - 123 (2007/10/03)

The reactions of 4-(methylamino)-3-penten-2-one with diazoketones yielded the α-acylenaminoketones 1-3 in good yields. Preparation of the α-acylenaminoketone 4 was carried out by treatment of 4-(t-butylamino)-3-penten-2-one with benzoyl chloride being followed by reaction of transamination with methylamine. The reactions were carried out in five different solvents and were submitted to gas chromatography/mass spectrometry analysis, with the goal of obtaining substituted pyrazoles and determining which of the carbonyls would preferentially be attacked by the nucleophile. The reactions of compounds 1-4 with hydrazine reagents led to the formation of the pyrazoles 5-7a-q. Small amounts of 4-methylamino-2-pentenones 10a-q, amides 11a-q and pyrazoles 12a-q were also obtained in these reactions. The unexpected formation of pyrazoles 15d,h,q was detected when methanol and N,N-dimethylformamide were used as solvents in the reactions of α-acylenaminoketone 4 with hydrazine reagents.

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