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1,3,5-Benzenetriol, 2-(3-methylbutyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 26104-00-7 Structure
  • Basic information

    1. Product Name: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-
    2. Synonyms:
    3. CAS NO:26104-00-7
    4. Molecular Formula: C11H16O3
    5. Molecular Weight: 196.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 26104-00-7.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: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(26104-00-7)
    11. EPA Substance Registry System: 1,3,5-Benzenetriol, 2-(3-methylbutyl)-(26104-00-7)
  • 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: 26104-00-7(Hazardous Substances Data)

26104-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26104-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,0 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26104-00:
(7*2)+(6*6)+(5*1)+(4*0)+(3*4)+(2*0)+(1*0)=67
67 % 10 = 7
So 26104-00-7 is a valid CAS Registry Number.

26104-00-7Relevant articles and documents

Antiprotozoal and antimicrobial activities of O-alkylated and formylated acylphloroglucinols

Bharate, Sandip B.,Khan, Shabana I.,Yunus, Nafees A.M.,Chauthe, Siddheshwar K.,Jacob, Melissa R.,Tekwani, Babu L.,Khan, Ikhlas A.,Singh, Inder Pal

, p. 87 - 96 (2007/10/03)

In the present article, we examined the antileishmanial, antimalarial, antibacterial, and antifungal activities of several newly synthesized O-alkylated phloroglucinol compounds (11-19) which are analogues of the naturally occurring antimalarial compound

An efficient two-step synthesis of jensenone isolated from Eucalyptus jensenii. Synthesis of analogues and evaluation as antioxidants

Bharate, Sandip B.,Chauthe, Siddheshwar K.,Bhutani, Kamlesh K.,Singh, Inder P.

, p. 551 - 555 (2007/10/03)

A phloroglucinol derivative, jensenone (1) isolated from leaves of Eucalyptus jensenii has been synthesized for the first time through a short and efficient two-step procedure starting from commercially available phloroglucinol. The methodology provides a simplified route to introduce diformyl moiety for synthesis of biologically active formylated phloroglucinol compounds such as antimalarial robustadials, cancer chemopreventive euglobals, and antifouling sideroxylonals. Several analogues of jensenone have also been synthesized and evaluated for antioxidant capacity. CSIRO 2005.

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