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N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415686-72-4 Structure
  • Basic information

    1. Product Name: N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester
    2. Synonyms: N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester
    3. CAS NO:1415686-72-4
    4. Molecular Formula:
    5. Molecular Weight: 647.852
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415686-72-4.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: N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester(1415686-72-4)
    11. EPA Substance Registry System: N-(2-acetoxybenzoyl)-L-alanine diosgenyl ester(1415686-72-4)
  • 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: 1415686-72-4(Hazardous Substances Data)

1415686-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415686-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,8 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1415686-72:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*8)+(3*6)+(2*7)+(1*2)=174
174 % 10 = 4
So 1415686-72-4 is a valid CAS Registry Number.

1415686-72-4Downstream Products

1415686-72-4Relevant articles and documents

Synthesis, characterization and biological studies of diosgenyl analogues

Huang, Baozhan,Du, Dan,Zhang, Rui,Wu, Xiaohua,Xing, Zhihua,He, Yang,Huang, Wen

, p. 7330 - 7334 (2013/02/23)

A series of optical amino acid diosgenyl esters and diosgenyl salicylate conjugates were designed and synthesized to develop new anticancer and anti-inflammatory agents. The analogue 9c that contains an 6-aminohexanoic acid residue at C-3 of diosgenin exhibits higher potency against all three tumor cell lines with IC50 values ranging from 4.7 μM in C26 cells to 14.6 μM in Hep G2 cells. In addition, seven of newly synthesized compounds significantly inhibit xylene-induced ear edema and exhibit comparable or better anti-inflammatory activities than those of diosgenin and aspirin. Furthermore, preliminary structure-activity relationship studies demonstrate that diosgenyl salicylate conjugates have stronger anti-inflammatory activities than amino acid diosgenyl esters.

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