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(R)-methyl 2-methyl-1,2,3,4-tetrahydroquinoline-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1446211-19-3 Structure
  • Basic information

    1. Product Name: (R)-methyl 2-methyl-1,2,3,4-tetrahydroquinoline-2-carboxylate
    2. Synonyms:
    3. CAS NO:1446211-19-3
    4. Molecular Formula:
    5. Molecular Weight: 205.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1446211-19-3.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: (R)-methyl 2-methyl-1,2,3,4-tetrahydroquinoline-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-methyl 2-methyl-1,2,3,4-tetrahydroquinoline-2-carboxylate(1446211-19-3)
    11. EPA Substance Registry System: (R)-methyl 2-methyl-1,2,3,4-tetrahydroquinoline-2-carboxylate(1446211-19-3)
  • 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: 1446211-19-3(Hazardous Substances Data)

1446211-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1446211-19-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,6,2,1 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1446211-19:
(9*1)+(8*4)+(7*4)+(6*6)+(5*2)+(4*1)+(3*1)+(2*1)+(1*9)=133
133 % 10 = 3
So 1446211-19-3 is a valid CAS Registry Number.

1446211-19-3Downstream Products

1446211-19-3Relevant articles and documents

Copper-catalyzed enantioselective intramolecular N -arylation, an efficient method for kinetic resolutions

Yang, Wenqiang,Long, Yan,Zhang, Shasha,Zeng, Youlin,Cai, Qian

, p. 3598 - 3601 (2013)

For the first time, copper-catalyzed intramolecular N-arylation was successfully applied to the kinetic resolution strategy. Under the catalysis of CuI-BINOL derived ligands, the kinetic resolution of rac-2-amino-3-(2-iodoaryl) propionates and rac-2-amino-4-(2-iodoaryl)butanoates afforded chiral intramolecular coupling products and recovered the starting materials in high enantioselectivity (s factors up to 245).

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