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2-(2-BOC-AMINOPHENYL)BENZALDEHYDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 138590-41-7 Structure
  • Basic information

    1. Product Name: 2-(2-BOC-AMINOPHENYL)BENZALDEHYDE
    2. Synonyms: 2-(2-BOC-AMINOPHENYL)BENZALDEHYDE
    3. CAS NO:138590-41-7
    4. Molecular Formula: C18H19NO3
    5. Molecular Weight: 297.34836
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 138590-41-7.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: 2-(2-BOC-AMINOPHENYL)BENZALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-BOC-AMINOPHENYL)BENZALDEHYDE(138590-41-7)
    11. EPA Substance Registry System: 2-(2-BOC-AMINOPHENYL)BENZALDEHYDE(138590-41-7)
  • Safety Data

    1. Hazard Codes: Xi,N
    2. Statements: 36/37/38-50/53
    3. Safety Statements: 26-36-60-61
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 138590-41-7(Hazardous Substances Data)

138590-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138590-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,9 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138590-41:
(8*1)+(7*3)+(6*8)+(5*5)+(4*9)+(3*0)+(2*4)+(1*1)=147
147 % 10 = 7
So 138590-41-7 is a valid CAS Registry Number.

138590-41-7Downstream Products

138590-41-7Relevant articles and documents

THE DIRECTED METALATION CONNECTION TO ARYL-ARYL CROSS COUPLING. REGIOSPECIFIC SYNTHESIS OF PHENANTHRIDINES, PHENANTHRIDINONES AND THE BIPHENYL ALKALOID ISMINE

Siddiqui, M.A.,Snieckus, V.

, p. 5463 - 5466 (2007/10/02)

Concise general routes to phenanthridines 4 and phenanthridinones 5 based on directed ortho metalation and cross coupling tactics are described; a short synthesis of the Amaryllidaceae alkaloid ismine (8b) is reported.

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