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CAS

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122571-34-0

Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122571-34-0 Structure

  • Basic information

    1. Product Name: Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI)
    2. Synonyms: Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI)
    3. CAS NO:122571-34-0
    4. Molecular Formula: C8H12O2
    5. Molecular Weight: 140.17968
    6. EINECS: N/A
    7. Product Categories: ALDEHYDE
    8. Mol File: 122571-34-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI)(122571-34-0)
    11. EPA Substance Registry System: Cyclohexanecarboxaldehyde, 2-methyl-4-oxo-, cis- (9CI)(122571-34-0)

  • 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: 122571-34-0(Hazardous Substances Data)

122571-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122571-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,7 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 122571-34:
(8*1)+(7*2)+(6*2)+(5*5)+(4*7)+(3*1)+(2*3)+(1*4)=100
100 % 10 = 0
So 122571-34-0 is a valid CAS Registry Number.

122571-34-0Downstream Products

122571-34-0Relevant articles and documents

CHEMISTRY OF ENOL ETHERS. LXXXVI. DIENE CONDENSATION OF 2-TRIMETHYLSILYLOXY-1,3-DIENES WITH α,β-UNSATURATED ALDEHYDES. 1-FORMYL-4-TRIMETHYLSILYLOXY-3-CYCLOHEXENES AND 1-FORMYL-4-OXOCYCLOHEXANES

Makin, S. M.,Shavrygina, O. A.,Nguyen, Fong Tung

, p. 2082 - 2087 (2007/10/02)

The diene condensation of a series of 2-trimethylsilyloxy-1,3-dienes (2-trimethylsilyloxy-1,3-butadiene, 2-trimethylsilyloxy-1,3-pentadiene, 2-trimethylsilyloxy-4-methyl-1,3-pentadiene) with acrylaldehyde and crotonaldehyde is distinguished by high regioselectivity and low stereoselectivity.The "para" adducts (1-formyl-4-trimethylsilyloxy-3-cyclohexenes) are formed exclusively in all cases, and the reaction leads to the formation of a mixture of the cis and trans isomers with respect to the asymmetric centers.Alcoholysis or acid hydrolysis of 1-formyl-4-trimethylsilyloxy-3-cyclohexenes give high yields of 1-formyl-4-oxocyclohexanes.In a number of cases the diene condensation is accompanied by the formation of undesirable side compounds, produced as a result of transsilylation, which takes place between the 2-trimethylsilyloxy-1,3-diene and crotonaldehyde used in the reaction.

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