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905978-05-4

1,3-bis(diacetoxymethyl)-2-bromo-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 905978-05-4 Structure

  • Basic information

    1. Product Name: 1,3-bis(diacetoxymethyl)-2-bromo-benzene
    2. Synonyms: 1,3-bis(diacetoxymethyl)-2-bromo-benzene
    3. CAS NO:905978-05-4
    4. Molecular Formula:
    5. Molecular Weight: 417.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 905978-05-4.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-bis(diacetoxymethyl)-2-bromo-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-bis(diacetoxymethyl)-2-bromo-benzene(905978-05-4)
    11. EPA Substance Registry System: 1,3-bis(diacetoxymethyl)-2-bromo-benzene(905978-05-4)

  • 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: 905978-05-4(Hazardous Substances Data)

905978-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 905978-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,9,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 905978-05:
(8*9)+(7*0)+(6*5)+(5*9)+(4*7)+(3*8)+(2*0)+(1*5)=204
204 % 10 = 4
So 905978-05-4 is a valid CAS Registry Number.

905978-05-4Relevant articles and documents

Diels-alder reactivity of binuclear complexes with calixarene-like structures

Kaess, Steffen,Gregor, Thomas,Kersting, Berthold

, p. 101 - 104 (2006)

The regioselectivity of the Diels-Alder reaction between ω-substituted dienoates and unsymmetrical dienophiles can be strictly controlled by "calixarene-like" metal complexes of type A (see scheme). The reaction of the dienoate coligand in A with acrylonitrile leads to the exclusive formation of the regioisomer adduct I, which is in striking contrast to the low regioselectivity of the background reaction. (Chemical Equation Presented).

Synthesis of chiral acetals by asymmetric selenenylations

Uehlin, Lars,Wirth, Thomas

experimental part, p. 1374 - 1385 (2010/03/03)

Asymmetric selenenylations of (E)-ethoxystyrene are described leading to chiral acetals. An efficient synthesis of such compounds including the determination of their absolute configuration is described.

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