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1160169-13-0

(E)-3-amino-2-phenylbut-2-enenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1160169-13-0 Structure

  • Basic information

    1. Product Name: (E)-3-amino-2-phenylbut-2-enenitrile
    2. Synonyms: (E)-3-amino-2-phenylbut-2-enenitrile
    3. CAS NO:1160169-13-0
    4. Molecular Formula:
    5. Molecular Weight: 158.203
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1160169-13-0.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: (E)-3-amino-2-phenylbut-2-enenitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-amino-2-phenylbut-2-enenitrile(1160169-13-0)
    11. EPA Substance Registry System: (E)-3-amino-2-phenylbut-2-enenitrile(1160169-13-0)

  • 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: 1160169-13-0(Hazardous Substances Data)

1160169-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1160169-13-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,1,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1160169-13:
(9*1)+(8*1)+(7*6)+(6*0)+(5*1)+(4*6)+(3*9)+(2*1)+(1*3)=120
120 % 10 = 0
So 1160169-13-0 is a valid CAS Registry Number.

1160169-13-0Upstream product

1160169-13-0Downstream Products

1160169-13-0Relevant articles and documents

Simple conversion of enamines to 2h-azirines and their rearrangements under thermal conditions

Li, Xiaoxun,Du, Yunfei,Liang, Zhidan,Li, Xiangke,Pan, Yan,Zhao, Kang

, p. 2643 - 2646 (2009)

A variety of substituted enamine derivatives were first found to be conveniently converted to the corresponding 2H-azirines mediated by phenyliodine (III) diacetate (PIDA). The formed 2-aryl-2W-azirines could be applied in the synthesis of indole-3-carbon

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