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2-Oxazolidinone, 3-[(2E)-3-(2-chloro-3-pyridinyl)-1-oxo-2-propenyl]-4-phenyl-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 494841-70-2 Structure
  • Basic information

    1. Product Name: 2-Oxazolidinone, 3-[(2E)-3-(2-chloro-3-pyridinyl)-1-oxo-2-propenyl]-4-phenyl-, (4S)-
    2. Synonyms:
    3. CAS NO:494841-70-2
    4. Molecular Formula: C17H13ClN2O3
    5. Molecular Weight: 328.755
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 494841-70-2.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: 2-Oxazolidinone, 3-[(2E)-3-(2-chloro-3-pyridinyl)-1-oxo-2-propenyl]-4-phenyl-, (4S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Oxazolidinone, 3-[(2E)-3-(2-chloro-3-pyridinyl)-1-oxo-2-propenyl]-4-phenyl-, (4S)-(494841-70-2)
    11. EPA Substance Registry System: 2-Oxazolidinone, 3-[(2E)-3-(2-chloro-3-pyridinyl)-1-oxo-2-propenyl]-4-phenyl-, (4S)-(494841-70-2)
  • 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: 494841-70-2(Hazardous Substances Data)

494841-70-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494841-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,8,4 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 494841-70:
(8*4)+(7*9)+(6*4)+(5*8)+(4*4)+(3*1)+(2*7)+(1*0)=192
192 % 10 = 2
So 494841-70-2 is a valid CAS Registry Number.

494841-70-2Downstream Products

494841-70-2Relevant articles and documents

Asymmetric synthesis of a selective endothelin a receptor antagonist

Kato, Yoshiaki,Niiyama, Kenji,Jona, Hideki,Okada, Shigemitsu,Akao, Atsushi,Hiraga, Shouichi,Tsuchiya, Yoshimi,Tomimoto, Koji,Mase, Toshiaki

, p. 1066 - 1072 (2007/10/03)

An asymmetric synthesis of a selective endothelin A receptor antagonist 1b is described. Asymmetric conjugate addition of aryllithium derived from 18 to the chiral oxazoline 17 followed by hydrolysis afforded 15 in 96% ee via purification as (S)-(-)-1-phe

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