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CAS

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1281969-63-8

2,4,6-trimethylbenzyl cyclohexanecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1281969-63-8 Structure

  • Basic information

    1. Product Name: 2,4,6-trimethylbenzyl cyclohexanecarboxylate
    2. Synonyms: 2,4,6-trimethylbenzyl cyclohexanecarboxylate
    3. CAS NO:1281969-63-8
    4. Molecular Formula:
    5. Molecular Weight: 260.376
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1281969-63-8.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: 2,4,6-trimethylbenzyl cyclohexanecarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4,6-trimethylbenzyl cyclohexanecarboxylate(1281969-63-8)
    11. EPA Substance Registry System: 2,4,6-trimethylbenzyl cyclohexanecarboxylate(1281969-63-8)

  • 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: 1281969-63-8(Hazardous Substances Data)

1281969-63-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1281969-63-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,1,9,6 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1281969-63:
(9*1)+(8*2)+(7*8)+(6*1)+(5*9)+(4*6)+(3*9)+(2*6)+(1*3)=198
198 % 10 = 8
So 1281969-63-8 is a valid CAS Registry Number.

1281969-63-8Downstream Products

1281969-63-8Relevant articles and documents

Nickel-catalyzed selective conversion of two different aldehydes to cross-coupled esters

Hoshimoto, Yoichi,Ohashi, Masato,Ogoshi, Sensuke

, p. 4668 - 4671 (2011)

In the presence of a Ni(0)/NHC catalyst, an equimolar mixture of aliphatic and aryl aldehydes can be employed to selectively yield a single cross-coupled ester. This reaction can be applied to a variety of aliphatic (1°, 2°, cyc-2°, and 3°) and aryl aldehyde combinations. The reaction represents 100% atom efficiency and generates no waste. Mechanistic studies have revealed that the striking feature of the reaction is the simultaneous coordination of two aldehydes to Ni(0).

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