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CAS

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1159919-04-6

3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1159919-04-6 Structure

  • Basic information

    1. Product Name: 3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone
    2. Synonyms: 3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone
    3. CAS NO:1159919-04-6
    4. Molecular Formula:
    5. Molecular Weight: 266.189
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1159919-04-6.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: 3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone(1159919-04-6)
    11. EPA Substance Registry System: 3,3,5-trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohexanone(1159919-04-6)

  • 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: 1159919-04-6(Hazardous Substances Data)

1159919-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1159919-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,9,1 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1159919-04:
(9*1)+(8*1)+(7*5)+(6*9)+(5*9)+(4*1)+(3*9)+(2*0)+(1*4)=186
186 % 10 = 6
So 1159919-04-6 is a valid CAS Registry Number.

1159919-04-6Downstream Products

1159919-04-6Relevant articles and documents

Mechanism of NHC-Catalyzed Conjugate Additions of Diboron and Borosilane Reagents to α,β-Unsaturated Carbonyl Compounds

Wu, Hao,Garcia, Jeannette M.,Haeffner, Fredrik,Radomkit, Suttipol,Zhugralin, Adil R.,Hoveyda, Amir H.

, p. 10585 - 10602 (2015)

Broadly applicable enantioselective C-B and C-Si bond-forming processes catalyzed by an N-heterocyclic carbene (NHC) were recently introduced; these boryl and silyl conjugate addition reactions (BCA and SCA, respectively), which proceed without the need f

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