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773109-21-0

Propanedioic acid, [(dimethylamino)methylene]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 773109-21-0 Structure

  • Basic information

    1. Product Name: Propanedioic acid, [(dimethylamino)methylene]- (9CI)
    2. Synonyms: Propanedioic acid, [(dimethylamino)methylene]- (9CI)
    3. CAS NO:773109-21-0
    4. Molecular Formula: C6H9NO4
    5. Molecular Weight: 159.13996
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 773109-21-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Propanedioic acid, [(dimethylamino)methylene]- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Propanedioic acid, [(dimethylamino)methylene]- (9CI)(773109-21-0)
    11. EPA Substance Registry System: Propanedioic acid, [(dimethylamino)methylene]- (9CI)(773109-21-0)

  • 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: 773109-21-0(Hazardous Substances Data)

773109-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773109-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,1,0 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 773109-21:
(8*7)+(7*7)+(6*3)+(5*1)+(4*0)+(3*9)+(2*2)+(1*1)=160
160 % 10 = 0
So 773109-21-0 is a valid CAS Registry Number.

773109-21-0Relevant articles and documents

Catalytic enamines from dialkylamide-dialkylacetals

Davey, Roger M.,Stamford, N. Patrick J.

scheme or table, p. 2537 - 2539 (2012/06/30)

The formation of a transient enamine derived from DMF-DMA provides an effective alternative to the harsh conditions normally required for the nucleophilic addition of base-activated methylene compounds to a carbonyl group. Organocatalysts formed from dialkylamide-dialkylacetals in this manner may provide extensive synthetic utility for a number of well-established reactions in which the formation of enolates and enamines has been employed.

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