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5,5-dimethyl-2-(4-(oct-1-yn-1-yl)phenyl)-1,3,2-dioxaborinane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034330-16-9 Structure
  • Basic information

    1. Product Name: 5,5-dimethyl-2-(4-(oct-1-yn-1-yl)phenyl)-1,3,2-dioxaborinane
    2. Synonyms:
    3. CAS NO:1034330-16-9
    4. Molecular Formula:
    5. Molecular Weight: 298.233
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034330-16-9.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: 5,5-dimethyl-2-(4-(oct-1-yn-1-yl)phenyl)-1,3,2-dioxaborinane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,5-dimethyl-2-(4-(oct-1-yn-1-yl)phenyl)-1,3,2-dioxaborinane(1034330-16-9)
    11. EPA Substance Registry System: 5,5-dimethyl-2-(4-(oct-1-yn-1-yl)phenyl)-1,3,2-dioxaborinane(1034330-16-9)
  • 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: 1034330-16-9(Hazardous Substances Data)

1034330-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034330-16-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,3,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1034330-16:
(9*1)+(8*0)+(7*3)+(6*4)+(5*3)+(4*3)+(3*0)+(2*1)+(1*6)=89
89 % 10 = 9
So 1034330-16-9 is a valid CAS Registry Number.

1034330-16-9Downstream Products

1034330-16-9Relevant articles and documents

Copper(I)-catalyzed carboxylation of aryl- and alkenylboronic esters

Takaya, Jun,Tadami, Satoshi,Ukai, Kazutoshi,Iwasawa, Nobuharu

, p. 2697 - 2700 (2008)

(Chemical Equation Presented) The copper(I)-catalyzed carboxylation reaction of aryl- and alkenylboronic esters proceeded smoothly under CO 2 to give the corresponding carboxylic acid in good yield. This reaction showed wide generality with higher functional group tolerance compared to the corresponding Rh(I)-catalyzed reaction.

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