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CAS

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488082-67-3

Benzoic acid, 3-[[2-(acetylamino)-5-iodophenyl]ethynyl]-5-iodo-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 488082-67-3 Structure

  • Basic information

    1. Product Name: Benzoic acid, 3-[[2-(acetylamino)-5-iodophenyl]ethynyl]-5-iodo-, methyl ester
    2. Synonyms:
    3. CAS NO:488082-67-3
    4. Molecular Formula: C18H13I2NO3
    5. Molecular Weight: 545.115
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 488082-67-3.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: Benzoic acid, 3-[[2-(acetylamino)-5-iodophenyl]ethynyl]-5-iodo-, methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3-[[2-(acetylamino)-5-iodophenyl]ethynyl]-5-iodo-, methyl ester(488082-67-3)
    11. EPA Substance Registry System: Benzoic acid, 3-[[2-(acetylamino)-5-iodophenyl]ethynyl]-5-iodo-, methyl ester(488082-67-3)

  • 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: 488082-67-3(Hazardous Substances Data)

488082-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 488082-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,0,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 488082-67:
(8*4)+(7*8)+(6*8)+(5*0)+(4*8)+(3*2)+(2*6)+(1*7)=193
193 % 10 = 3
So 488082-67-3 is a valid CAS Registry Number.

488082-67-3Relevant articles and documents

Hydrogen Bond-Stabilized Helix Formation of a m-Phenylene Ethynylene Oligomer

Cary, Jennifer M.,Moore, Jeffrey S.

, p. 4663 - 4666 (2007/10/03)

(Matrix Presented) Incorporation of a single hydrogen bonded β-turn mimic in the backbone of a m-phenylene ethynylene oligomer is shown to affect the thermodynamic properties of the folding reaction. Oligomers 1 and 2 both undergo solvophobic helix formation, but hydrogen bonded oligomer 1 was found to form a more stable helix with a higher tolerance to solvent denaturation than isomeric, non-hydrogen bonded oligomer 2.

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