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544669-15-0

N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 544669-15-0 Structure

  • Basic information

    1. Product Name: N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide
    2. Synonyms: N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide;N-(2-chloro-5-nitro-phenyl)-2-cyano-ethanamide;STK317955
    3. CAS NO:544669-15-0
    4. Molecular Formula: C9H6ClN3O3
    5. Molecular Weight: 239.61524
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 544669-15-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide(544669-15-0)
    11. EPA Substance Registry System: N-(2-chloro-5-nitrophenyl)-2-cyanoacetamide(544669-15-0)

  • 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: 544669-15-0(Hazardous Substances Data)

544669-15-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 544669-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,4,6,6 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 544669-15:
(8*5)+(7*4)+(6*4)+(5*6)+(4*6)+(3*9)+(2*1)+(1*5)=180
180 % 10 = 0
So 544669-15-0 is a valid CAS Registry Number.

544669-15-0Relevant articles and documents

Synthesis of 7-substituted pyrazolo[1,5-a]pyrimidine-3-carboxamides as potential non benzodiazepine hypnotics

Behbehani, Haider,Ibrahim, Hamada Mohamed,Makhseed, Saad

experimental part, p. 267 - 282 (2010/08/07)

A variety of new pyrazolo[1,5-a]pyrimidines has been prepared as potential drugs for the treatment of insomnia. The general synthetic route used for this purpose involves the condensation of substituted cyanoacetamides 5a-c, prepared by reaction of cyanoacetic acid with amines in presence of acetic anhydride, with dimethylformamide dimethylacetal and subsequent treatment of the formed enamines 6 with hydrazine hydrate. This process affords the corresponding aminopyrazole carboxamides 9 that react with the enaminonitrile 12 to generate the targets. Structures of the substance prepared in these sequences were established by using spectroscopic methods, including 15N HMBC and NOE difference experiments, as well as X-raycrystallographic analysis.

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