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166331-37-9

trans (S)-(-)-N-methyl-N-(2-propylaldehyde) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 166331-37-9 Structure

  • Basic information

    1. Product Name: trans (S)-(-)-N-methyl-N-(2-propylaldehyde)
    2. Synonyms: trans (S)-(-)-N-methyl-N-(2-propylaldehyde)
    3. CAS NO:166331-37-9
    4. Molecular Formula:
    5. Molecular Weight: 217.268
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 166331-37-9.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: trans (S)-(-)-N-methyl-N-(2-propylaldehyde)(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans (S)-(-)-N-methyl-N-(2-propylaldehyde)(166331-37-9)
    11. EPA Substance Registry System: trans (S)-(-)-N-methyl-N-(2-propylaldehyde)(166331-37-9)

  • 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: 166331-37-9(Hazardous Substances Data)

166331-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166331-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,3 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 166331-37:
(8*1)+(7*6)+(6*6)+(5*3)+(4*3)+(3*1)+(2*3)+(1*7)=129
129 % 10 = 9
So 166331-37-9 is a valid CAS Registry Number.

166331-37-9Upstream product

166331-37-9Downstream Products

166331-37-9Relevant articles and documents

α-Amino Acids as Chiral Educts for Stereoselective Syntheses of Pyrrolidine and Pyrrolizidine Systems

Chiacchio, Ugo,Casuscelli, Franco,Corsaro, Antonio,Librando, Vito,Rescifina, Antonio,et al.

, p. 5689 - 5700 (1995)

Homochiral functionalized pyrrolidine and pyrrolizidine systems have been achieved by stereoselective intramolecular 1,3-dipolar cycloaddition of homochiral nitrones, starting from homochiral amino acids, and by subsequent reduction of the obtained cycloadducts.

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