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CAS

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141245-84-3

Acetamide, N-[4-(5-chloro-6-nitro-1H-benzimidazol-2-yl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141245-84-3 Structure

  • Basic information

    1. Product Name: Acetamide, N-[4-(5-chloro-6-nitro-1H-benzimidazol-2-yl)phenyl]-
    2. Synonyms:
    3. CAS NO:141245-84-3
    4. Molecular Formula: C15H11ClN4O3
    5. Molecular Weight: 330.73
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141245-84-3.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: Acetamide, N-[4-(5-chloro-6-nitro-1H-benzimidazol-2-yl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[4-(5-chloro-6-nitro-1H-benzimidazol-2-yl)phenyl]-(141245-84-3)
    11. EPA Substance Registry System: Acetamide, N-[4-(5-chloro-6-nitro-1H-benzimidazol-2-yl)phenyl]-(141245-84-3)

  • 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: 141245-84-3(Hazardous Substances Data)

141245-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141245-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,2,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 141245-84:
(8*1)+(7*4)+(6*1)+(5*2)+(4*4)+(3*5)+(2*8)+(1*4)=103
103 % 10 = 3
So 141245-84-3 is a valid CAS Registry Number.

141245-84-3Relevant articles and documents

SYNTHESIS AND STRUCTURE OF MONOCHLORO DERIVATIVES OF 2-(4-AMINOPHENYL)-5(6)-AMINOBENZIMIDAZOLE

Shchel'tsyn, V. K.,Frolova, T. I.,Grudtsyn, Yu. D.,Vandysheva, E. A.,Kaminskii, A. Ya.,Leonova, V. V.

, p. 2132 - 2142 (2007/10/02)

Methods for the production of the monochloro derivatives of 2-(4-aminophenyl)-5(6)-aminobenzimidazole from chloronitrobenzanilides or by the condensation of 1,2,4-triaminobenzene with chloroaminobenzoic acid were investigated.It was established that the nitration of o-chlorobenzanilides takes place selectively in a mixture of acetic acid, acetic anhydride, and chloroform, while the nitration of 4(7)- or 5(6)-chlorobenzimidazoles takes place in sulfuric acid.The effect of the chlorine atoms and the nitro (amino) group on the IR and PMR spectra of the benzanilides and benzimidazoles is determined by their mutual position and by the position in relation of the amide bridge or the condensed imidazole ring.Analysis of the PMR spectra of the chlorodiaminophenylbenzimidazoles indicated that the amino group was localized at position 6 of the benzimidazole ring.

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