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1393825-29-0

(S)-13-(trityloxy)tridecan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1393825-29-0 Structure

  • Basic information

    1. Product Name: (S)-13-(trityloxy)tridecan-2-ol
    2. Synonyms: (S)-13-(trityloxy)tridecan-2-ol
    3. CAS NO:1393825-29-0
    4. Molecular Formula:
    5. Molecular Weight: 458.684
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1393825-29-0.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: (S)-13-(trityloxy)tridecan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-13-(trityloxy)tridecan-2-ol(1393825-29-0)
    11. EPA Substance Registry System: (S)-13-(trityloxy)tridecan-2-ol(1393825-29-0)

  • 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: 1393825-29-0(Hazardous Substances Data)

1393825-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1393825-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,8,2 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1393825-29:
(9*1)+(8*3)+(7*9)+(6*3)+(5*8)+(4*2)+(3*5)+(2*2)+(1*9)=190
190 % 10 = 0
So 1393825-29-0 is a valid CAS Registry Number.

1393825-29-0Relevant articles and documents

CAL-B catalyzed synthesis of chiral polyamides

Poulhes, Florent,Mouysset, Dominique,Gil, Gerard,Bertrand, Michele P.,Gastaldi, Stephane

, p. 867 - 875 (2012)

CAL-B (Novozym 435) plays a dual role in our approach to chiral polyamides. It is used to introduce the appropriate chirality in the synthesis of monomers (amino-esters and diamines) from racemic 12-methyldodecalactone and then to catalyze their polycondensation. The AB and AABB enzymatic polymerizations have been carried out under reduced pressure; they give rise to optically active polymers in good yield, with a good degree of polymerization, and a narrow polydispersity index. This approach demonstrates that the presence of a methyl group at the stereogenic center at the α-position relative to the nitrogen atom does not slow down the polymerization as compared with the polycondensation of a related achiral monomer.

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