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5744-59-2

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5744-59-2 Usage

Chemical Properties

White solid

Check Digit Verification of cas no

The CAS Registry Mumber 5744-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,4 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5744-59:
(6*5)+(5*7)+(4*4)+(3*4)+(2*5)+(1*9)=112
112 % 10 = 2
So 5744-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O2/c1-4-3-5(6(9)10)7-8(4)2/h3H,1-2H3,(H,9,10)

5744-59-2 Well-known Company Product Price

  • Brand
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  • Alfa Aesar

  • (H64475)  1,5-Dimethyl-1H-pyrazole-3-carboxylic acid, 98%   

  • 5744-59-2

  • 1g

  • 290.0CNY

  • Detail
  • Alfa Aesar

  • (H64475)  1,5-Dimethyl-1H-pyrazole-3-carboxylic acid, 98%   

  • 5744-59-2

  • 5g

  • 1156.0CNY

  • Detail
  • Alfa Aesar

  • (H64475)  1,5-Dimethyl-1H-pyrazole-3-carboxylic acid, 98%   

  • 5744-59-2

  • 25g

  • 4831.0CNY

  • Detail
  • Aldrich

  • (722359)  1,5-Dimethyl-1H-pyrazole-3-carboxylicacid  97%

  • 5744-59-2

  • 722359-1G

  • 1,102.14CNY

  • Detail

5744-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,5-Dimethyl-1H-pyrazole-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1,5-dimethylpyrazole-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:5744-59-2 SDS

5744-59-2Relevant articles and documents

PYRAZOLE DERIVATIVES AS H4 ANTAGONIST COMPOUNDS

-

, (2020/05/21)

The disclosures herein relate to novel compounds of formula (1): and salts thereof, wherein A; X;n; R1 and R2 are defined herein, and their use in treating, preventing, ameliorating, controlling or reducing the risk of disorders associated with H4 receptors.

3-Isoxazoyl derivatives endowed with anticonvulsant activity, procedure for their preparation and their pharmaceutical compositions

-

, (2008/06/13)

The object of the invention is heterocyclic compounds of general formula (I) endowed with anticonvulsant activity: STR1 in which Y is selected from --O--, --S-- and STR2 R4 being H or optionally substituted alkyl, acyl or benzyl, Z is selected

Pyrazolodiazepines. 1,3 (and 2,3) dialkyl 4,6 dihydro 8 arylpyrazolo[4,3 e][1,4] diazepin 5 ones as antianxiety agents

DeWald,Nordin,L'Italien,Parcell

, p. 1346 - 1354 (2007/10/04)

A series of 1, 3 (and 2, 3) dialkyl 4, 6 dihydro 8 arylpyrazolo [4, 3 e][1, 4] diazepin 5 ones was synthesized and evaluated for psychotropic activity. Intermediates are new dialkylnitropyrazolyl aryl ketones prepared from dialkylnitropyrazolecarboxylic acids. Many of these pyrazolodiazepines exhibit high CNS activity in animals. One compound, 1 ethyl 4, 6 dihydro 3 methyl 8 phenylpyrazolo [4, 3 e] [1, 4] diazepin 5 (1H) one is about as potent as diazepam as an antianxiety agent with less sedative properties and is being studied in the clinic.

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