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ALLYLBENZENE-2,3,4,5,6-D5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126245-60-1 Structure
  • Basic information

    1. Product Name: ALLYLBENZENE-2,3,4,5,6-D5
    2. Synonyms: ALLYLBENZENE-2,3,4,5,6-D5
    3. CAS NO:126245-60-1
    4. Molecular Formula: C9H10
    5. Molecular Weight: 123.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126245-60-1.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: ALLYLBENZENE-2,3,4,5,6-D5(CAS DataBase Reference)
    10. NIST Chemistry Reference: ALLYLBENZENE-2,3,4,5,6-D5(126245-60-1)
    11. EPA Substance Registry System: ALLYLBENZENE-2,3,4,5,6-D5(126245-60-1)
  • 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: 126245-60-1(Hazardous Substances Data)

126245-60-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126245-60-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,2,4 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126245-60:
(8*1)+(7*2)+(6*6)+(5*2)+(4*4)+(3*5)+(2*6)+(1*0)=111
111 % 10 = 1
So 126245-60-1 is a valid CAS Registry Number.

126245-60-1Downstream Products

126245-60-1Relevant articles and documents

Palladium-Catalyzed meta-C-H Olefination of Arene-Tethered Diols Directed by Well-Designed Pyrimidine-Based Group

Fang, Siqiang,Wang, Xiaobing,Yin, Fucheng,Cai, Pei,Yang, Huali,Kong, Lingyi

supporting information, (2019/03/19)

The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimidine moiety is presented. Applications of the protocol are illustrated by the synthesis of various diol-based natural products, such as coumarins, phenylpropanoids, stilbenes, and chalcones. Advantages of this method are demonstrated through the easy removal of the template and a gram-scale olefination reaction. Finally, experimental verification, including 1H NMR, ESI-MS and IR, and DFT studies are undertaken to elucidate the mechanistic complexity.

Umpolung of Reactivity of Allylsilane, Allylgermane, and Allylstannane: Allylation of Aromatic Compounds with Allylmetal and Allylthallium Bis(trifluoroacetate)

Ochiai, Masahito,Fujita, Eiichi,Arimoto, Masao,Yamaguchi, Hideo

, p. 3994 - 3999 (2007/10/02)

A direct allylation of aromatic compounds using allylsilane, allylgermane, or allylstannane (1) and arylthallium bis(trifluoroacetate) has been developed.The actual transmetalation reagent for 1 in the reaction was proposed to be thallium (III) trifluoroacetate (2), which was proposed together with diarylthallium trifluoroacetate by the disproportionation of arylthallium bis(trifluoroacetate).Keywords-allylation of aromatic compound; allylsilane; allylgermane; allylstannane; arylthallium bis(trifluoroacetate)

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