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  • 163626-07-1 Structure
  • Basic information

    1. Product Name: C12H18Br2OTe
    2. Synonyms: C12H18Br2OTe
    3. CAS NO:163626-07-1
    4. Molecular Formula:
    5. Molecular Weight: 465.682
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 163626-07-1.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: C12H18Br2OTe(CAS DataBase Reference)
    10. NIST Chemistry Reference: C12H18Br2OTe(163626-07-1)
    11. EPA Substance Registry System: C12H18Br2OTe(163626-07-1)
  • 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: 163626-07-1(Hazardous Substances Data)

163626-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163626-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,6,2 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 163626-07:
(8*1)+(7*6)+(6*3)+(5*6)+(4*2)+(3*6)+(2*0)+(1*7)=131
131 % 10 = 1
So 163626-07-1 is a valid CAS Registry Number.

163626-07-1Downstream Products

163626-07-1Relevant articles and documents

3H(3R)-benzo-2,1-oxatelluroles as synthons in synthesis of o-alkyltellurophenyl carbonyl compounds

Sadekov, Igor D.,Maksimenko, Alexander A.,Minkin, Vladimir I.

, p. 3365 - 3374 (2007/10/03)

A convenient method, developed for the preparation of o-alkyltelluro-benzaldehydes and -phenyl-ketones from o-alkyltellurobenzyl alcohols, involves the intermediate formation and rearrangement of 3H(3R)-benzo-2,1-oxatelluroles, a novel tellurium-containin

5H-1,2-OXATELLUROLES AND THEIR BENZO ANALOGS: SYNTHESIS AND REACTIONS

Sadekov, I. D.,Maksimenko, A. A.,Zakharov, A. V.,Rivkin, B. B.

, p. 243 - 254 (2007/10/02)

Tetracoordinated derivatives of 2-halo-2-aryl-5H-1,2-oxatelluroles and 1-halo-1-butyl-3H-benz-2,1-oxatelluroles were synthesized by the oxidation of 3-aryltelluro-2-propen-1-ols and the dehydrogenation of 2-butyldihalotellurobenzyl alcohols.The halogen at

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