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3-Cyclopropyl-5-nitro-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 326827-23-0 Structure
  • Basic information

    1. Product Name: 3-Cyclopropyl-5-nitro-1H-pyrazole
    2. Synonyms: 3-Cyclopropyl-5-nitro-1H-pyrazole;3-cyclopropyl-5-nitro-2H-pyrazole
    3. CAS NO:326827-23-0
    4. Molecular Formula: C6H7N3O2
    5. Molecular Weight: 153.13868
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 326827-23-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 351.1±30.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.519±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.88±0.10(Predicted)
    10. CAS DataBase Reference: 3-Cyclopropyl-5-nitro-1H-pyrazole(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Cyclopropyl-5-nitro-1H-pyrazole(326827-23-0)
    12. EPA Substance Registry System: 3-Cyclopropyl-5-nitro-1H-pyrazole(326827-23-0)
  • 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: 326827-23-0(Hazardous Substances Data)

326827-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326827-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,8,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 326827-23:
(8*3)+(7*2)+(6*6)+(5*8)+(4*2)+(3*7)+(2*2)+(1*3)=150
150 % 10 = 0
So 326827-23-0 is a valid CAS Registry Number.

326827-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyclopropyl-5-nitro-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3-cyclopropylisonicotinaldehyde

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:326827-23-0 SDS

326827-23-0Downstream Products

326827-23-0Relevant articles and documents

3-Acylaminopyrazole derivatives via a regioselectively N-protected 3-nitropyrazole

Orsini, Paolo,Traquandi, Gabriella,Sansonna, Pietro,Pevarello, Paolo

, p. 933 - 935 (2005)

A simple procedure for the selective protection of the endocyclic 1-N of 3-aminopyrazoles as tert-butoxycarbamate (Boc) in good yield is described. A 3-nitropyrazole derivative represents the key intermediate with the nitro substituent determining the regiochemistry of the obtained protected compound. Subsequent acylation at the exocyclic amino group gave rise, after Boc removal, to a series of 3-acylaminopyrazoles in high yields and purities.

3(5)-ureido-pyrazole derivatives process for their preparation and their use as antitumor agents

-

, (2008/06/13)

3-ureido-pyrazole derivatives represented by formula (I): where R, R1and R2are as described herein, or pharmnaceutically acceptable salts thereof; are useful, for example, for the treatment of cancer, cell proliferative disorders, Alzheimer's disease, viral infections, auto-immune diseases or neurodegenerative diseases.

3(5)-amino-pyrazole derivatives, process for their preparation and their use as antitumor agents

-

, (2008/06/13)

Compounds which are 3-amino-pyrazole derivatives represented by formula (I): where R is a C3-C6cycloalkyl group, which may optionally be substituted by a straight or branched C1-C6alkyl group, and R1is a straight or branched C1-C6alkyl group or a C2-C4alkenyl, cycloalkyl, aryl, arylalkyl, arylcarbonyl, aryloxyalkyl and arylalkenyl, which may be optionally substituted; or a pharmaceutically acceptable salt thereof. The compounds are useful for the treatment of cancer, cell proliferative disorders, Alzheimer's disease, viral infections, auto-immune diseases or neurodegenerative diseases.

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