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3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 151166-75-5 Structure
  • Basic information

    1. Product Name: 3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde
    2. Synonyms: 3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde
    3. CAS NO:151166-75-5
    4. Molecular Formula: C17H26O3
    5. Molecular Weight: 278
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151166-75-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde(151166-75-5)
    11. EPA Substance Registry System: 3,5-di-tert-butyl-4-(methoxymethoxy)benzaldehyde(151166-75-5)
  • 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: 151166-75-5(Hazardous Substances Data)

151166-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151166-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,1,6 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 151166-75:
(8*1)+(7*5)+(6*1)+(5*1)+(4*6)+(3*6)+(2*7)+(1*5)=115
115 % 10 = 5
So 151166-75-5 is a valid CAS Registry Number.

151166-75-5Downstream Products

151166-75-5Relevant articles and documents

Peroxynitrite generation from a NO-releasing nitrobenzene derivative in response to photoirradiation

Ieda, Naoya,Nakagawa, Hidehiko,Horinouchi, Taeko,Peng, Tao,Yang, Dan,Tsumoto, Hiroki,Suzuki, Takayoshi,Fukuhara, Kiyoshi,Miyata, Naoki

supporting information; experimental part, p. 6449 - 6451 (2011/06/27)

Photocontrollable ONOO- generation from a nitrobenzene derivative was demonstrated. The designed compound released NO in response to photoirradiation, and the resulting semiquinone reduced molecular oxygen to generate O2-; reaction of the two generated ONOO -, as confirmed with an ONOO- fluorescent probe, HKGreen-3.

Antioxidant activity of hydroxystilbene derivatives in homogeneous solution

Amorati, Riccardo,Lucarini, Marco,Mugnaini, Veronica,Pedulli, Gian Franco,Roberti, Marinella,Pizzirani, Daniela

, p. 7101 - 7107 (2007/10/03)

The antioxidant activity of the cis and trans isomers of several analogues of resveratrol and pterostilbene has been investigated, especially with regard to the effect of the stereochemistry about the olefinic double bond. The antioxidant power of these c

Development of a new class of potential antiatherosclerosis agents: NO-donor antioxidants

Cena, Clara,Boschi, Donatella,Tron, Gian Cesare,Chegaev, Kostantin,Lazzarato, Loretta,Stilo, Antonella Di,Aragno, Manuela,Fruttero, Roberta,Gasco, Alberto

, p. 5971 - 5974 (2007/10/03)

A new class of NO-donor phenol derivatives is described. The products were obtained by joining appropriate phenols with either nitrooxy or 3-phenylsulfonylfuroxan-4-yloxy moieties. All the compounds proved to inhibit the ferrous salt/ascorbate induced lip

Use of aryl nitrone compounds in methods for treating neuropathic pain

-

, (2008/06/13)

3,4,5-trisubstituted aryl nitrone compounds having the formula: where R1—R4 are as defined in the specification are useful as therapeutics for neuropathic pain conditions in mammals.

3,4,5-trisubstituted aryl nitrone compounds, pharmaceutical compositions containing the same and methods for treating inflammation

-

Page column 20-21, (2008/06/13)

Disclosed are 3,4,5-trisubstituted aryl nitrone compounds and pharmaceutical compositions containing such compounds. The 3,4,5-trisubstituted aryl nitrone compounds have the formula: where R1-R4are as defined in the specification. The disclosed compositions are useful as therapeutics for inflammation-related conditions in mammals, such as arthritis, and as analytical reagents for detecting free radicals.

Novel antiarthritic agents with 1,2-isothiazolidine-1-,1-dioxide (γ- sultam) skeleton: Cytokine suppressive dual inhibitors of cyclooxygenase-2 and 5-lipoxygenase

Inagaki, Masanao,Tsuri, Tatsuo,Jyoyama, Hirokuni,Ono, Takashi,Yamada, Katsutoshi,Kobayashi, Mika,Hori, Yozo,Arimura, Akinori,Yasui, Kiyoshi,Ohno, Kouji,Kakudo, Shinji,Koizumi, Kenzo,Suzuki, Ryuji,Kato, Miyako,Kawai, Shinichi,Matsumoto, Saichi

, p. 2040 - 2048 (2007/10/03)

Various 1,2-isothiazolidine-1,1-dioxide (γ-sultam) derivatives containing an antioxidant moiety, 2,6-di-tert-butylphenol substituent, were prepared. Some compounds, which have a lower alkyl group at the 2-position of the γ-sultam skeleton, showed potent i

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