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CAS

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1448538-66-6

(R)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448538-66-6 Structure

  • Basic information

    1. Product Name: (R)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate
    2. Synonyms: (R)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate
    3. CAS NO:1448538-66-6
    4. Molecular Formula:
    5. Molecular Weight: 382.459
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448538-66-6.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)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate(1448538-66-6)
    11. EPA Substance Registry System: (R)-tert-butyl (1-methyl-2-oxo-3-phenethoxyindolin-3-yl)carbamate(1448538-66-6)

  • 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: 1448538-66-6(Hazardous Substances Data)

1448538-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448538-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,5,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1448538-66:
(9*1)+(8*4)+(7*4)+(6*8)+(5*5)+(4*3)+(3*8)+(2*6)+(1*6)=196
196 % 10 = 6
So 1448538-66-6 is a valid CAS Registry Number.

1448538-66-6Downstream Products

1448538-66-6Relevant articles and documents

Catalytic enantioselective addition of alcohols to isatin-derived N-Boc ketimines

Li, Tian-Ze,Wang, Xi-Bo,Sha, Feng,Wu, Xin-Yan

, p. 7314 - 7319 (2013)

The enantioselective addition of alcohols to isatin-derived N-Boc ketimines was investigated for the first time. Isatin-derived N,O-aminals were obtained in excellent yields with moderate-to-good enantioselectivities (up to 78% ee) in the presence of a quinine-based bifunctional catalyst.

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