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CAS

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1086452-24-5

(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1086452-24-5 Structure

  • Basic information

    1. Product Name: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate
    2. Synonyms: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate
    3. CAS NO:1086452-24-5
    4. Molecular Formula:
    5. Molecular Weight: 264.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1086452-24-5.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: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate(1086452-24-5)
    11. EPA Substance Registry System: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-diazopent-4-enoate(1086452-24-5)

  • 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: 1086452-24-5(Hazardous Substances Data)

1086452-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1086452-24-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,6,4,5 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1086452-24:
(9*1)+(8*0)+(7*8)+(6*6)+(5*4)+(4*5)+(3*2)+(2*2)+(1*4)=155
155 % 10 = 5
So 1086452-24-5 is a valid CAS Registry Number.

1086452-24-5Relevant articles and documents

Convenient synthetic route to an enantiomerically pure FMOC α-amino acid

Taber, Douglass F.,Berry, James F.,Martin, Timothy J.

supporting information; experimental part, p. 9334 - 9339 (2009/04/06)

(Chemical Equation Presented) A strategy for the facile α-amination of carboxylic acid menthyl esters is described. The resulting diastereomers, readily separable, can be individually carried on to each enantiomer of the FMOC α-amino acid. A variety of un

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