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CAS

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923283-85-6

1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester

    Cas No: 923283-85-6

  • USD $ 1.9-2.9 / Gram

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  • 923283-85-6 Structure

  • Basic information

    1. Product Name: 1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester
    2. Synonyms:
    3. CAS NO:923283-85-6
    4. Molecular Formula: C8H11N3O4
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 923283-85-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester(923283-85-6)
    11. EPA Substance Registry System: 1H-Pyrazole-3-carboxylic acid, 1-(1-methylethyl)-4-nitro-, methyl ester(923283-85-6)

  • 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: 923283-85-6(Hazardous Substances Data)

923283-85-6 Usage

Structure

Pyrazole-3-carboxylic acid derivative with a methyl ester group, an isopropyl group, and a nitro group

Type

Chemical compound

Uses

Organic synthesis, pharmaceutical research (as a building block for the synthesis of various compounds), reference standard in analytical chemistry (for identification and quantification of similar compounds), and investigation for potential pharmacological properties and biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 923283-85-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,2,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 923283-85:
(8*9)+(7*2)+(6*3)+(5*2)+(4*8)+(3*3)+(2*8)+(1*5)=176
176 % 10 = 6
So 923283-85-6 is a valid CAS Registry Number.

923283-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-nitro-1-propan-2-ylpyrazole-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:923283-85-6 SDS

923283-85-6Relevant articles and documents

PYRROLOPYRIDAZINE INHIBITORS OF IRAK4 ACTIVITY

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Page/Page column 34, (2016/09/26)

The present invention relates to pyrrolopyridazine inhibitors of IRAK4 of formula (I) and provides compositions comprising such inhibitors, as well as methods therewith for treating IRAK4-mediated or -associated conditions or diseases.

PYRAZOLOPYRIMIDINE INHIBITORS OF IRAK4 ACTIVITY

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Page/Page column 55, (2016/09/26)

The present invention relates to pyrazolopyrimidine inhibitors of IRAK4 of formula (I) and provides compositions comprising such inhibitors, as well as methods therewith for treating IRAK4-mediated or -associated conditions or diseases.

Pyrazolo pyrimidines useful as aurora kinase inhibitors

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Page/Page column 100, (2010/11/25)

The present invention provides compounds having the formula: wherein A-B together represent one of the following structures: wherein one of is a double bond, as valency permits; and R2, R4, X1A, X2A, X1B, X2B, L1, L2, Y and Z are as defined in classes and subclasses herein, and pharmaceutical compositions thereof, as described generally and in subclasses herein, which compounds are useful as inhibitors of protein kinase (e.g., Aurora), and thus are useful, for example, for the treatment of Aurora mediated diseases.

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