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CAS

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34644-27-4

2-dimethylamino-2-ethoxy-1-cyanoethylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 34644-27-4 Structure

  • Basic information

    1. Product Name: 2-dimethylamino-2-ethoxy-1-cyanoethylene
    2. Synonyms: 2-dimethylamino-2-ethoxy-1-cyanoethylene
    3. CAS NO:34644-27-4
    4. Molecular Formula:
    5. Molecular Weight: 140.185
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 34644-27-4.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-dimethylamino-2-ethoxy-1-cyanoethylene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-dimethylamino-2-ethoxy-1-cyanoethylene(34644-27-4)
    11. EPA Substance Registry System: 2-dimethylamino-2-ethoxy-1-cyanoethylene(34644-27-4)

  • 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: 34644-27-4(Hazardous Substances Data)

34644-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34644-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,4 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34644-27:
(7*3)+(6*4)+(5*6)+(4*4)+(3*4)+(2*2)+(1*7)=114
114 % 10 = 4
So 34644-27-4 is a valid CAS Registry Number.

34644-27-4Relevant articles and documents

Hydrogenolysis of Amide Acetals and Iminium Esters

Kadyrov, Renat

, p. 170 - 172 (2017/12/26)

Amide acetals and iminium esters were hydrogenated into amines under very mild reaction conditions over common hydrogenation catalysts. This finding provides a new strategy for the selective reduction of amides. The synthetic utility of this approach was demonstrated by the selective reduction of amides bearing ester and nitrile groups.

Orthoamides, XXXIV.-Syntheses with Vinylidenediamines

Kantlehner, Willi,Ivanov, Ivo C.,Mergen, Walter W.,Bredereck, Hellmut

, p. 372 - 388 (2007/10/02)

Vinylidenediamines 2a,c have been prepared from 1-ethoxyvinylamine 4 and dimethylamine or pyrrolidine, respectively.Heating of 2a and formamidinium acetate affords 4-amino-5-pyrimidinecarbonitrile (7b).Acylation of 2a with acid chlorides or acid anhydride

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