Welcome to LookChem.com Sign In|Join Free

CAS

  • or
3-amino-4-chloro-1H-pyrazole-5-carboxylic acid (SALTDATA: FREE) is a pyrazole derivative chemical compound characterized by the molecular formula C5H5ClN4O2. It features a chlorine atom and an amino group attached to the pyrazole ring, which endows it with unique chemical properties and potential applications in various fields.

351990-69-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 351990-69-7 Structure
  • Basic information

    1. Product Name: 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
    2. Synonyms: 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE);3-aMino-4-chloro-1H-pyrazole-5-carboxylic acid;3-aMino-4-chloropyrazole-5-carboxylic acid;5-amino-4-chloro-2H-pyrazole-3-carboxylic acid
    3. CAS NO:351990-69-7
    4. Molecular Formula: C4H4ClN3O2
    5. Molecular Weight: 161.54646
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 351990-69-7.mol
  • Chemical Properties

    1. Melting Point: 287-288 °C(Solv: water (7732-18-5))
    2. Boiling Point: 475.0±45.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.841±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 14.79±0.50(Predicted)
    10. CAS DataBase Reference: 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)(351990-69-7)
    12. EPA Substance Registry System: 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)(351990-69-7)
  • 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: 351990-69-7(Hazardous Substances Data)

351990-69-7 Usage

Uses

Used in Pharmaceutical Research and Development:
3-amino-4-chloro-1H-pyrazole-5-carboxylic acid (SALTDATA: FREE) is utilized as a key intermediate in the synthesis of new drugs, particularly for the development of pharmaceuticals with novel therapeutic properties. Its unique structure allows for the creation of more complex organic molecules, which can be further explored for their potential medicinal applications.
Used in Organic Synthesis:
In the field of organic chemistry, 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid (SALTDATA: FREE) serves as a building block for the synthesis of more complex organic molecules. Its versatile functional groups enable chemists to modify and extend its structure, leading to the discovery of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 351990-69-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,9,9 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 351990-69:
(8*3)+(7*5)+(6*1)+(5*9)+(4*9)+(3*0)+(2*6)+(1*9)=167
167 % 10 = 7
So 351990-69-7 is a valid CAS Registry Number.
InChI:InChI=1S/C4H4ClN3O2/c5-1-2(4(9)10)7-8-3(1)6/h(H,9,10)(H3,6,7,8)

351990-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4-chloro-1H-pyrazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Amino-4-chloro-1H-pyrazole-3-carboxylic acid

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:351990-69-7 SDS

351990-69-7Downstream Products

351990-69-7Relevant articles and documents

Nitropyrazoles : 118. Synthesis and transformations of 5-amino-3,4- dinitropyrazole

Dalinger,Vatsadse,Shkineva,Popova,Ugrak,Shevelev

experimental part, p. 1631 - 1638 (2011/05/03)

A method of preparation of 5-amino-3,4-dinitropyrazole (1) from 3(5)-methyl-5(3)-nitro- and 3(5)-methyl-4,5(3)-dinitropyrazoles was developed, the key step of which was the Hofmann rearrengement of nitro- and dinitropyrazolecarboxamides. The protonation o

COMPOUNDS, COMPOSITIONS AND METHODS FOR CONTROL OF HEPATITIS C VIRAL INFECTIONS

-

Page/Page column 55, (2010/09/17)

Various tetrahydropyrazolo[1,5-a]pyrimidine compounds, compositions, methods of making, and methods for the prevention and treatment of HCV infections and associated diseases are disclosed. The invention further relates to biomarkers for identification of HCV strains which are resistant to the tetrahydropyrazolo[1,5- a]pyrimidine compounds.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 351990-69-7