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89869-02-3

2-(benzyloxy)-2-cyclohexylacetaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89869-02-3 Structure

  • Basic information

    1. Product Name: 2-(benzyloxy)-2-cyclohexylacetaldehyde
    2. Synonyms: 2-(benzyloxy)-2-cyclohexylacetaldehyde
    3. CAS NO:89869-02-3
    4. Molecular Formula:
    5. Molecular Weight: 232.323
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89869-02-3.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: 2-(benzyloxy)-2-cyclohexylacetaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(benzyloxy)-2-cyclohexylacetaldehyde(89869-02-3)
    11. EPA Substance Registry System: 2-(benzyloxy)-2-cyclohexylacetaldehyde(89869-02-3)

  • 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: 89869-02-3(Hazardous Substances Data)

89869-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89869-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89869-02:
(7*8)+(6*9)+(5*8)+(4*6)+(3*9)+(2*0)+(1*2)=203
203 % 10 = 3
So 89869-02-3 is a valid CAS Registry Number.

89869-02-3Relevant articles and documents

Aniline mediated oxidative C-C bond cleavage of α-alkoxy aldehydes in air and a model reaction for the synthesis of α-(d)-amino acid derivatives

Hu, Bin,Li, Yunfeng,Li, Zhongjun,Meng, Xiangbao

supporting information, p. 4138 - 4141 (2013/07/05)

A metal-free and 4-methyl aniline mediated method for the oxidative C-C bond cleavage has been developed. The reaction proceeds in air using molecular oxygen as the oxidant, affording one-carbon shortened esters in moderate to good yields within a short time. Moreover, it provides a model reaction for the highly enantioselective synthesis of (d)-serine esters by combining with a l-proline catalyzed Mannich reaction.

Super-acid Catalysed Addition of Allylsilanes to Carbonyl Compounds; Synthetic and Mechanistic Aspects

Davis, Anthony P.,Jaspars, Marcel

, p. 2111 - 2118 (2007/10/02)

The addition of allyltrimethylsilane 8 to a variety of aldehydes and one ketone (cyclohexanone) was found to be induced by the super-acid TfOH2(1+)B(OTf)4(1-) (Tf = CF3SO2).In contrast to the analogous Lewis acid catalysed reaction, only catalytic amounts

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