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CAS

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124667-88-5

2'-O-acetyl-4-O-(4-acetylbenzyl)tylosin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124667-88-5 Structure

  • Basic information

    1. Product Name: 2'-O-acetyl-4-O-(4-acetylbenzyl)tylosin
    2. Synonyms: 2'-O-acetyl-4-O-(4-acetylbenzyl)tylosin
    3. CAS NO:124667-88-5
    4. Molecular Formula:
    5. Molecular Weight: 1090.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124667-88-5.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'-O-acetyl-4-O-(4-acetylbenzyl)tylosin(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2'-O-acetyl-4-O-(4-acetylbenzyl)tylosin(124667-88-5)
    11. EPA Substance Registry System: 2'-O-acetyl-4-O-(4-acetylbenzyl)tylosin(124667-88-5)

  • 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: 124667-88-5(Hazardous Substances Data)

124667-88-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124667-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,6,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124667-88:
(8*1)+(7*2)+(6*4)+(5*6)+(4*6)+(3*7)+(2*8)+(1*8)=145
145 % 10 = 5
So 124667-88-5 is a valid CAS Registry Number.

124667-88-5Downstream Products

124667-88-5Relevant articles and documents

Application of dibutyltin oxide method to regioselective acylation and alkylation of tylosin at C-4''.

Kiyoshima,Sakamoto,Ishikura,Fukagawa,Yoshioka,Naganawa,Sawa,Takeuchi

, p. 861 - 865 (2007/10/02)

4''-O-Acyl-, 4''-O-alkyl- and 4''-deoxy-tylosin derivatives were synthesized using 2'-O-acetyl-3'',4''-O-(dibutyl-stannio)tylosin as a synthetic intermediate. The in vitro biological evaluation showed that the new derivatives were active against macrolide-resistant clinical isolates of bacteria and mycoplasmas, and that they were resistant to hepatic esterase.

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