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102912-90-3

N-(4-(((4-chlorophenyl)imino)methyl)phenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 102912-90-3 Structure

  • Basic information

    1. Product Name: N-(4-(((4-chlorophenyl)imino)methyl)phenyl)acetamide
    2. Synonyms:
    3. CAS NO:102912-90-3
    4. Molecular Formula:
    5. Molecular Weight: 272.734
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 102912-90-3.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: N-(4-(((4-chlorophenyl)imino)methyl)phenyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(4-(((4-chlorophenyl)imino)methyl)phenyl)acetamide(102912-90-3)
    11. EPA Substance Registry System: N-(4-(((4-chlorophenyl)imino)methyl)phenyl)acetamide(102912-90-3)

  • 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: 102912-90-3(Hazardous Substances Data)

102912-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102912-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,1 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102912-90:
(8*1)+(7*0)+(6*2)+(5*9)+(4*1)+(3*2)+(2*9)+(1*0)=93
93 % 10 = 3
So 102912-90-3 is a valid CAS Registry Number.

102912-90-3Downstream Products

102912-90-3Relevant articles and documents

Umpolung Addition of Aldehydes to Aryl Imines

Chen, Ning,Dai, Xi-Jie,Wang, Haining,Li, Chao-Jun

, p. 6260 - 6263 (2017)

One of the classical ways to synthesize amines involves the coupling of carbonyl compounds and imines, either through enolate chemistry or acyl-based carbanion equivalents. We herein report an alternative strategy that is based on the use of aldehydes as alkyl carbanion equivalents in a reductive coupling with aryl imines. A wide array of secondary amines can be synthesized in moderate to high yields. This reaction is mediated by hydrazine and catalyzed by ruthenium(II) complexes, and it tolerates various functional groups, such as esters, amides, and nitriles.

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