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Hexane, 1,1-dimethoxy-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116549-35-0 Structure
  • Basic information

    1. Product Name: Hexane, 1,1-dimethoxy-2-methyl-
    2. Synonyms:
    3. CAS NO:116549-35-0
    4. Molecular Formula: C9H20O2
    5. Molecular Weight: 160.257
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116549-35-0.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: Hexane, 1,1-dimethoxy-2-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Hexane, 1,1-dimethoxy-2-methyl-(116549-35-0)
    11. EPA Substance Registry System: Hexane, 1,1-dimethoxy-2-methyl-(116549-35-0)
  • 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: 116549-35-0(Hazardous Substances Data)

116549-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116549-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116549-35:
(8*1)+(7*1)+(6*6)+(5*5)+(4*4)+(3*9)+(2*3)+(1*5)=130
130 % 10 = 0
So 116549-35-0 is a valid CAS Registry Number.

116549-35-0Downstream Products

116549-35-0Relevant articles and documents

Selective hydroformylation-acetalization of various olefins using simple and efficient Rh-phosphinite complex catalyst

Khan, Shoeb R.,Bhanage, Bhalchandra M.

, p. 5998 - 6001 (2013)

A simple and efficient Rh-phosphinite complex catalyst was studied for the selective hydroformylation of various olefins. The influence of various reaction parameters including the effect of temperature, pressure, catalyst loading, time, and solvents was studied. The protocol was also applied for the synthesis of various acetals via tandem hydroformylation-acetalization of olefins in alcohols as solvents. High activity and selectivity for acetal formation was achieved in the absence of co-catalysts with admirable substrate to catalyst mole ratio (TON 2500). The developed protocol works for a wide range of olefins to synthesize corresponding aldehydes and acetals under optimized reaction conditions.

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