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1038891-20-1

2-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1038891-20-1 Structure

  • Basic information

    1. Product Name: 2-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile
    2. Synonyms: 2-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile
    3. CAS NO:1038891-20-1
    4. Molecular Formula:
    5. Molecular Weight: 328.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1038891-20-1.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-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile(1038891-20-1)
    11. EPA Substance Registry System: 2-[(4-methylbenzyl)amino]-2-(3-phenoxyphenyl)acetonitrile(1038891-20-1)

  • 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: 1038891-20-1(Hazardous Substances Data)

1038891-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1038891-20-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,8,8,9 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1038891-20:
(9*1)+(8*0)+(7*3)+(6*8)+(5*8)+(4*9)+(3*1)+(2*2)+(1*0)=161
161 % 10 = 1
So 1038891-20-1 is a valid CAS Registry Number.

1038891-20-1Downstream Products

1038891-20-1Relevant articles and documents

Rhodium(III) iodide hydrate catalyzed three-component coupling reaction: synthesis of α-aminonitriles from aldehydes, amines, and trimethylsilyl cyanide

Majhi, Anjoy,Kim, Sung Soo,Kadam, Santosh T.

, p. 5509 - 5514 (2008)

Aryl imines formed from aldehydes and amines undergo smoothly in situ nucleophilic addition with trimethylsilyl cyanide (TMSCN) in the presence of catalytic amount of hydrated rhodium(III) iodide to?afford the corresponding α-aminonitriles in excellent yield. The low catalytic loading (2 mol %), mild experimental conditions, and short reaction time (mostly within 13 min) represent the key features of this novel catalytic system.

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