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CAS

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917752-20-6

Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 917752-20-6 Structure

  • Basic information

    1. Product Name: Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester
    2. Synonyms: Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester
    3. CAS NO:917752-20-6
    4. Molecular Formula: C9H9NO3
    5. Molecular Weight: 179.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 917752-20-6.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: Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester(917752-20-6)
    11. EPA Substance Registry System: Carbamic acid, N-[3-(2-furanyl)-2-propen-1-ylidene]-, methyl ester(917752-20-6)

  • 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: 917752-20-6(Hazardous Substances Data)

917752-20-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 917752-20-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,7,5 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 917752-20:
(8*9)+(7*1)+(6*7)+(5*7)+(4*5)+(3*2)+(2*2)+(1*0)=186
186 % 10 = 6
So 917752-20-6 is a valid CAS Registry Number.

917752-20-6Downstream Products

917752-20-6Relevant articles and documents

CHIRAL AMINE-CATALYZED ASYMMETRIC ADDITION OF CARBON-CENTERED NUCLEOPHILES TO IMINES

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Page/Page column 73-74, (2010/11/25)

The present invention relates to an asymmetric synthesis useful for preparing compounds useful for the treatment of cardiovascular diseases and for studying the role of motor proteins in cell cycle progression.

Highly diastereoselective asymmetric Mannich reactions of 1,3-dicarbonyls with acyl imines

Ting, Amal,Lou, Sha,Schaus, Scott E.

, p. 2003 - 2006 (2007/10/03)

The cinchona alkaloids catalyze direct asymmetric Mannich reactions of cyclic 1,3-dicarbonyl compounds with acyl imines to afford α-quaternary carbon-bearing reaction products in yields of up to 98%, a diastereomeric excess of 90% or greater, and enantios

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