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854459-39-5

N1-phenyl-1,2-butanediamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 854459-39-5 Structure

  • Basic information

    1. Product Name: N1-phenyl-1,2-butanediamine
    2. Synonyms: N1-phenyl-1,2-butanediamine
    3. CAS NO:854459-39-5
    4. Molecular Formula:
    5. Molecular Weight: 164.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 854459-39-5.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: N1-phenyl-1,2-butanediamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N1-phenyl-1,2-butanediamine(854459-39-5)
    11. EPA Substance Registry System: N1-phenyl-1,2-butanediamine(854459-39-5)

  • 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: 854459-39-5(Hazardous Substances Data)

854459-39-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854459-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,4,5 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 854459-39:
(8*8)+(7*5)+(6*4)+(5*4)+(4*5)+(3*9)+(2*3)+(1*9)=205
205 % 10 = 5
So 854459-39-5 is a valid CAS Registry Number.

854459-39-5Downstream Products

854459-39-5Relevant articles and documents

Selective alkylation of (Hetero)aromatic amines with alcohols catalyzed by a ruthenium pincer complex

Agrawal, Santosh,Lenormand, Maud,Martin-Matute, Belen

supporting information; experimental part, p. 1456 - 1459 (2012/05/04)

A readily available pincer ruthenium(II) complex catalyzes the selective monoalkylation of (hetero)aromatic amines with a wide range of primary alcohols (including pyridine-, furan-, and thiophene-substituted alcohols) with high efficiency when used in low catalyst loadings (1 mol %). Tertiary amine formation via polyalkylation does not occur, making this ruthenium system an excellent catalyst for the synthesis of sec-amines.

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