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1068134-56-4

(2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1068134-56-4 Structure

  • Basic information

    1. Product Name: (2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate
    2. Synonyms: (2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate
    3. CAS NO:1068134-56-4
    4. Molecular Formula:
    5. Molecular Weight: 291.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1068134-56-4.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: (2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate(1068134-56-4)
    11. EPA Substance Registry System: (2R,4R)-2-phenyl-4-vinylthiazolidine-3-tert-butyl carboxylate(1068134-56-4)

  • 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: 1068134-56-4(Hazardous Substances Data)

1068134-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1068134-56-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,8,1,3 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1068134-56:
(9*1)+(8*0)+(7*6)+(6*8)+(5*1)+(4*3)+(3*4)+(2*5)+(1*6)=144
144 % 10 = 4
So 1068134-56-4 is a valid CAS Registry Number.

1068134-56-4Relevant articles and documents

Stereospecific total synthesis of somocystinamide A

Suyama, Takashi L.,Gerwick, William H.

, p. 4449 - 4452 (2008)

(Chemical Equation Presented) The first total synthesis of somocystinamide A, a disulfide dimer with extremely labile enamide functional groups, was accomplished in a concise and stereospecific manner. Somocystinamide A is reported to possess exceptionall

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