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CAS

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1392427-30-3

2-benzylaminomethyl-3,4-dimethyl-phosphaferrocene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1392427-30-3 Structure

  • Basic information

    1. Product Name: 2-benzylaminomethyl-3,4-dimethyl-phosphaferrocene
    2. Synonyms:
    3. CAS NO:1392427-30-3
    4. Molecular Formula:
    5. Molecular Weight: 351.211
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1392427-30-3.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: 2-benzylaminomethyl-3,4-dimethyl-phosphaferrocene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzylaminomethyl-3,4-dimethyl-phosphaferrocene(1392427-30-3)
    11. EPA Substance Registry System: 2-benzylaminomethyl-3,4-dimethyl-phosphaferrocene(1392427-30-3)

  • 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: 1392427-30-3(Hazardous Substances Data)

1392427-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392427-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,4,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1392427-30:
(9*1)+(8*3)+(7*9)+(6*2)+(5*4)+(4*2)+(3*7)+(2*3)+(1*0)=163
163 % 10 = 3
So 1392427-30-3 is a valid CAS Registry Number.

1392427-30-3Downstream Products

1392427-30-3Relevant articles and documents

On the immobilization of a monophosphaferrocene on a silica support

Komath Mallissery, Samith,Gudat, Dietrich

, p. 1141 - 1145 (2012)

Reactions of 2-formyl-3, 4-dimethyl-1-phosphaferrocene with aminopropyl (AP) functionalized hexagonal mesoporous silica (HMS) were studied in the absence and presence of an excess of the mild reducing agent Na[BH 3CN]. Starting material and reaction products were characterized by analytical and multinuclear (13C, 29Si, 31P) MAS NMR spectroscopic data. Both reactions proceeded by partial derivatization of surface-bound NH2 groups to yield products with tethered phosphaferrocene units. Evaluation of spectroscopic data and the results of homogeneous model reactions confirmed that condensation of both components gives imines, which are obviously kinetically labile and allow leakage of the tethered phosphaferrocene into solution. Reactions carried out in the presence of Na[BH3CN] proceed as reductive amination to yield secondary amines with enhanced kinetic stability. The reductive amination is accompanied by formation of minor amounts of phosphorus-containing by-products as well as the hydrolysis of surface bound ethoxy groups present in the starting material.

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