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1392008-12-6

(R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1392008-12-6 Structure

  • Basic information

    1. Product Name: (R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate
    2. Synonyms: (R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate
    3. CAS NO:1392008-12-6
    4. Molecular Formula:
    5. Molecular Weight: 357.247
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1392008-12-6.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: (R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate(1392008-12-6)
    11. EPA Substance Registry System: (R,E)-ethyl 2-(2-bromophenyl)-3-(tert-butyldiazenyl)-2-hydroxypropanoate(1392008-12-6)

  • 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: 1392008-12-6(Hazardous Substances Data)

1392008-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392008-12-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,0,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1392008-12:
(9*1)+(8*3)+(7*9)+(6*2)+(5*0)+(4*0)+(3*8)+(2*1)+(1*2)=136
136 % 10 = 6
So 1392008-12-6 is a valid CAS Registry Number.

1392008-12-6Downstream Products

1392008-12-6Relevant articles and documents

Asymmetric formal carbonyl-ene reactions of formaldehyde tert -butyl hydrazone with α-keto esters: Dual activation by bis-urea catalysts

Crespo-Pena, Ana,Monge, David,Martin-Zamora, Eloisa,Alvarez, Eleuterio,Fernandez, Rosario,Lassaletta, Jose M.

supporting information; experimental part, p. 12912 - 12915 (2012/09/25)

The dual activation of α-keto esters and formaldehyde tert-butyl hydrazone by BINAM-derived bis-ureas is the key to achieve high reactivity and excellent enantioselectivities in nucleophilic addition (formal carbonyl-ene reaction) to functionalized tertiary carbinols. Ensuing high-yielding diazene-to-aldehyde tranformations and subsequent derivatizations provides a direct entry to a variety of densely functionalized products.

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