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711012-11-2

(3-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 711012-11-2 Structure

  • Basic information

    1. Product Name: (3-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane
    2. Synonyms: (3-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane
    3. CAS NO:711012-11-2
    4. Molecular Formula:
    5. Molecular Weight: 361.351
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 711012-11-2.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-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane(711012-11-2)
    11. EPA Substance Registry System: (3-bromo-4-methoxymethoxy-benzyloxy)-tert-butyl-dimethyl-silane(711012-11-2)

  • 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: 711012-11-2(Hazardous Substances Data)

711012-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 711012-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,1,0,1 and 2 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 711012-11:
(8*7)+(7*1)+(6*1)+(5*0)+(4*1)+(3*2)+(2*1)+(1*1)=82
82 % 10 = 2
So 711012-11-2 is a valid CAS Registry Number.

711012-11-2Relevant articles and documents

A concise synthetic approach to dihydrochalcone: First total syntheses of bipinnatone A and B

Zhao, Xiao Long,Li, Hui Zhi,Zhang, Xian Shu,Wang, Wen Jing,Da, Shi Jun,Li, Ying

scheme or table, p. 1135 - 1138 (2012/01/06)

The first total syntheses of bipinnatone A and B have been achieved starting from commercially available phloroglucinol, p-hydroxybenzaldehyde in ten steps. Key features of the syntheses include Aldol reaction, aryl-alkylation and InCl3-NaBH4 selective reduction.

Efficient synthesis and structure-activity relationship of honokiol, a neurotrophic biphenyl-type neolignan

Esumi, Tomoyuki,Makado, Gouki,Zhai, Haifeng,Shimizu, Yasuhiro,Mitsumoto, Yasuhide,Fukuyama, Yoshiyasu

, p. 2621 - 2625 (2007/10/03)

Honokiol, a biphenyl-type neolignan, which shows the remarkable neurotrophic effect in primary cultured rat cortical neurons, has been effectively synthesized in 21% yield over 14 steps starting from 5-bromosalicylic acid and p-hydroxybenzoic acid by utilizing Pd-catalyzed Suzuki-Miyaura coupling reaction as a key step. Additionally, the structure-activity relationship between neurite outgrowth-promoting activity and its O-methylated and/or its hydrogenated analogues was examined in the primary cultures of fetal rat cortical neurons, suggesting that 5-allyl and 4′-hydroxyl groups are essential for affecting the neurotrophic activity of honokiol.

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