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CAS

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313705-62-3

B10H10C2(Si(CH3)2)2OCC(C6H5)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 313705-62-3 Structure

  • Basic information

    1. Product Name: B10H10C2(Si(CH3)2)2OCC(C6H5)2
    2. Synonyms: B10H10C2(Si(CH3)2)2OCC(C6H5)2
    3. CAS NO:313705-62-3
    4. Molecular Formula:
    5. Molecular Weight: 452.754
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 313705-62-3.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: B10H10C2(Si(CH3)2)2OCC(C6H5)2(CAS DataBase Reference)
    10. NIST Chemistry Reference: B10H10C2(Si(CH3)2)2OCC(C6H5)2(313705-62-3)
    11. EPA Substance Registry System: B10H10C2(Si(CH3)2)2OCC(C6H5)2(313705-62-3)

  • 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: 313705-62-3(Hazardous Substances Data)

313705-62-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313705-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,7,0 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 313705-62:
(8*3)+(7*1)+(6*3)+(5*7)+(4*0)+(3*5)+(2*6)+(1*2)=113
113 % 10 = 3
So 313705-62-3 is a valid CAS Registry Number.

313705-62-3Downstream Products

313705-62-3Relevant articles and documents

Nickel-catalyzed double silylation of a variety of carbonyl compounds with 1,2-bis(dimethylsilyl)carborane

Kang, Youngjin

, p. 5026 - 5031 (2000)

The nickel-catalyzed reactions of 1,2-bis(dimethylsilyl)carborane 1 with aldehydes such as isobutyraldehyde, trimethylacetaldehyde, hexanal, and benzaldehyde afforded 5,6-carboranylene-2-oxa-1,4-disilacyclohexanes. The dehydrogenative 1,4-double silylation of methacrolein and trans-4-phenyl-3-buten-2-one in the presence of a catalytic amount of Ni-(PEt3)4 took place under similar conditions. In contrast, the reaction of 1 with α-methyl-trans-cinnamaldehyde and trans-cinnamaldehyde under the same reaction conditions yielded the insertion compounds formed via insertion of a carbonyl group into each of the C-Si bonds of 1. The reaction of 1 with diphenylketene gave the 1,2-adduct across the carbonyl group. The structures of compounds 8, 11, and 14 were determined by single-crystal X-ray crystallography.

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