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CAS

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1332849-07-6

(-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1332849-07-6 Structure

  • Basic information

    1. Product Name: (-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate
    2. Synonyms: (-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate
    3. CAS NO:1332849-07-6
    4. Molecular Formula:
    5. Molecular Weight: 496.601
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1332849-07-6.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: (-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate(1332849-07-6)
    11. EPA Substance Registry System: (-)-benzyl (2R,3R,6S,8R)-8-O-[(S)-O'-acetylmandeloyl]bishomononactate(1332849-07-6)

  • 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: 1332849-07-6(Hazardous Substances Data)

1332849-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1332849-07-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,2,8,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1332849-07:
(9*1)+(8*3)+(7*3)+(6*2)+(5*8)+(4*4)+(3*9)+(2*0)+(1*7)=156
156 % 10 = 6
So 1332849-07-6 is a valid CAS Registry Number.

1332849-07-6Upstream product

1332849-07-6Downstream Products

1332849-07-6Relevant articles and documents

Synthesis of macrotetrolide α, a designed polynactin analog composed of bishomononactic acids

Takai, Kentaro,Hanadate, Tadaatsu,Abe, Masaki,Ono, Yukie,Yamada, Teiko,Kuwahara, Shigefumi,Kiyota, Hiromasa

, p. 7066 - 7072 (2011/10/05)

Macrotetrolide α (1), a designed polynactin analog composed of (+)- and (-)-bishomononactic acids, was synthesized. The monomeric acids were prepared using cis-selective iodoetherification and optical resolution of the corresponding O-acetylmandelates as the key steps. Esterification and macrolactonization of the monomers were performed by Corey-Mukaiyama-Gerlach method. Compound 1 showed no immunosuppressive activity contrary to other natural polynactin congeners.

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