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1445989-81-0

(S,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1445989-81-0 Structure

  • Basic information

    1. Product Name: (S,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one
    2. Synonyms: (S,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one
    3. CAS NO:1445989-81-0
    4. Molecular Formula:
    5. Molecular Weight: 375.556
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1445989-81-0.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,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one(1445989-81-0)
    11. EPA Substance Registry System: (S,E)-1-{(R)-4-benzyl-2-thioxothiazolidin-3-yl}-3-hydroxy-6-methylnona-6,8-dien-1-one(1445989-81-0)

  • 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: 1445989-81-0(Hazardous Substances Data)

1445989-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1445989-81-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,9,8 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1445989-81:
(9*1)+(8*4)+(7*4)+(6*5)+(5*9)+(4*8)+(3*9)+(2*8)+(1*1)=220
220 % 10 = 0
So 1445989-81-0 is a valid CAS Registry Number.

1445989-81-0Relevant articles and documents

Protection-free, short, and stereoselective synthesis of ieodomycin A and B

Nageswara Rao,Meshram

, p. 4544 - 4546 (2013)

A concise, protection-free, and improved stereoselective total synthesis of ieodomycin A and ieodomycin B is described. The key steps involved in the synthesis are Evans aldol reaction and nucleophilic addition of potassium salt of mono methyl malonate.

Stereoselective total synthesis of ieodomycins A and B and revision of the NMR spectroscopic data of ieodomycin B

Das, Sayantan,Goswami, Rajib Kumar

, p. 7274 - 7280 (2013/08/23)

Stereoselective total synthesis of antimicrobial marine metabolites ieodomycin A and B have been accomplished starting from commercially available 4-pentyn-1-ol featuring strategic application of the Negishi reaction, Kumada coupling, and Crimmins acetate aldol. This revises the proton NMR spectra of ieodomycin B.

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