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1352085-99-4

3-azido-4-carbonylpentyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1352085-99-4 Structure

  • Basic information

    1. Product Name: 3-azido-4-carbonylpentyl benzoate
    2. Synonyms: 3-azido-4-carbonylpentyl benzoate
    3. CAS NO:1352085-99-4
    4. Molecular Formula:
    5. Molecular Weight: 247.254
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1352085-99-4.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: 3-azido-4-carbonylpentyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-azido-4-carbonylpentyl benzoate(1352085-99-4)
    11. EPA Substance Registry System: 3-azido-4-carbonylpentyl benzoate(1352085-99-4)

  • 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: 1352085-99-4(Hazardous Substances Data)

1352085-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1352085-99-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,8 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1352085-99:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*8)+(3*5)+(2*9)+(1*9)=154
154 % 10 = 4
So 1352085-99-4 is a valid CAS Registry Number.

1352085-99-4Relevant articles and documents

COMPOUNDS HAVING ACTIVATING EFFECT ON SUBTYPES OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS AND ITS PREPARATION METHOD AND USES

-

, (2013/05/09)

Phenyl propanoic acid compounds having activating effect on peroxisome proliferator-activated receptors (PPARα,δ,γ) and a preparation method and uses thereof are provided in the present invention. The compounds can be used for treating or preventing diseases associated with peroxisome proliferator-activated receptors (PPARα,δ,γ).

Compounds Having Activating Effect on Subtypes of Peroxisome Proliferator-Activated Receptors and its Preparation Method and Uses

-

, (2013/04/13)

Phenyl propanoic acid compounds having activating effect on peroxisome proliferator-activated receptors (PPARα,δ,γ) and a preparation method and uses thereof are provided in the present invention. The compounds can be used for treating or preventing diseases associated with peroxisome proliferator-activated receptors (PPARα,δ,γ).

Design and synthesis of 3-(2-ethyl-4-{2-[2-(4-fluorophenyl)- 5-methyloxazol-4-yl]ethoxy}phenyl)propanoic acid: A novel triple-acting PPARα, -γ, and -δ Agonist

Zhang, Qijun,Sun, Peng,Zheng, Guojun,Wang, Yaping,Wang, Xiangjing,Wei, Hegeng,Xiang, Wensheng

, p. 406 - 408 (2012/06/01)

The design and synthesis of triple-acting PPARα, -γ, and -δ agonist 3-(2-ethyl-4-{2-[2-(4-fluorophenyl)-5-methyloxazol-4-yl]- ethoxy}phenyl)propanoic acid (1a) is described. The compound possesses a potent triple-acting PPARα, -γ, and -δ agonist profile with an EC50 of 0.029, 0.013, and 0.029 μM, respectively. The synthetic route, involving the synthesis of oxazole rings as the key step, starts from commercially available 3-oxopentanoic acid methyl ester and 3- hydroxyacetophenone to afford the target compound 1 with an overall yield of 32%.

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