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(E)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135064-81-2 Structure
  • Basic information

    1. Product Name: (E)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate
    2. Synonyms: (E)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate
    3. CAS NO:135064-81-2
    4. Molecular Formula:
    5. Molecular Weight: 315.329
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135064-81-2.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)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate(135064-81-2)
    11. EPA Substance Registry System: (E)-ethyl α-cyano-2-(pyrrolidin-1-yl)-5-nitrocinnamate(135064-81-2)
  • 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: 135064-81-2(Hazardous Substances Data)

135064-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135064-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,6 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 135064-81:
(8*1)+(7*3)+(6*5)+(5*0)+(4*6)+(3*4)+(2*8)+(1*1)=112
112 % 10 = 2
So 135064-81-2 is a valid CAS Registry Number.

135064-81-2Downstream Products

135064-81-2Relevant articles and documents

Highly stereoselective synthesis of 2-aminobenzylidene derivatives by a convergent 3-component approach

Xu, Zian,Ge, Jingying,Wang, Tianchi,Luo, Ting,Liu, Hongwei,Yu, Xinhong

, p. 2913 - 2917 (2014)

An one-pot stereoselective synthesis of 2-aminobenzylidene derivatives from readily available 5-nitro/cyano-activated 2-halobenzaldehydes (2-chloro-5-nitrobenzaldehyde, 2-bromo-5-nitrobenzaldehyde, 2-fluoro-5-nitrobenzaldehyde, 5-cyano-2-fluorobenzaldehyd

Stereochemical aspects of the "tert-amino effect". Controlled cycloreversion of pyrroloquinoline derivatives and enantioselective introduction of two new optically active centers

Kelderman, E.,Noorlander-Bunt, H. G.,Eerden, J. van,Verboom, W.,Reinhoudt, D. N.

, p. 115 - 123 (2007/10/02)

Conversion of 2-vinyl-N,N-dialkylanilines 2,3(a-o) to pyrroloquinolines 4-13(a-o) occurs via an irreversible suprafacial 1,5 hydrogen shift to a dipolar intermediate which subsequently cyclizes.In refluxing acetonitrile in the presence of zinc chlo

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