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2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 211105-00-9 Structure
  • Basic information

    1. Product Name: 2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester
    2. Synonyms: 2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester
    3. CAS NO:211105-00-9
    4. Molecular Formula: C13H17BrO2
    5. Molecular Weight: 285.17688
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 211105-00-9.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: 2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester(211105-00-9)
    11. EPA Substance Registry System: 2-(4-BroMoMethyl-phenyl)-2-Methyl-propionic acid ethyl ester(211105-00-9)
  • 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: 211105-00-9(Hazardous Substances Data)

211105-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211105-00-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,1,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 211105-00:
(8*2)+(7*1)+(6*1)+(5*1)+(4*0)+(3*5)+(2*0)+(1*0)=49
49 % 10 = 9
So 211105-00-9 is a valid CAS Registry Number.

211105-00-9Relevant articles and documents

Metabolites of (3-[[4-tert-butyl-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenoxy)-acetic acid

-

, (2008/06/13)

The present invention relates to metabolites of (3-{[4-tert-butyl-benzyl)-(pyridine-3-sulfonyl)-amino]-methyl}-phenoxy)-acetic acid.

Synthesis of terfenadine and derivatives

-

, (2008/06/13)

Processes for preparing compounds having the general formula: STR1 wherein R1a is protected carboxy, carboxy, hydroxymethyl, protected hydroxymethyl, or methyl are disclosed. Processes of the invention begin with a starting material of the general formula II STR2 and elaborate the product by reductive amination of an aldehyde of formula IVa STR3 with α,α-diphenyl-4-piperidinemethanol.

An efficient and facile synthesis of racemic and optically active fexofenadine

Fang, Qun K.,Senanayake, Chris H.,Wilkinson, H. Scott,Waid, Stephen A.,Li, Hui

, p. 2701 - 2704 (2007/10/03)

In efficient and practical method for the synthesis of racemic and optically active (96% ee) fexofenadine is described. The key racemic or optically active lactol intermediate 2 is prepared from readily available tolyl derivative 3.

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