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4-CHLOROADAMANTAN-1-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61357-37-7 Structure
  • Basic information

    1. Product Name: 4-CHLOROADAMANTAN-1-OL
    2. Synonyms: 4-CHLOROADAMANTAN-1-OL
    3. CAS NO:61357-37-7
    4. Molecular Formula: C10H15ClO
    5. Molecular Weight: 186.68
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61357-37-7.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: 4-CHLOROADAMANTAN-1-OL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-CHLOROADAMANTAN-1-OL(61357-37-7)
    11. EPA Substance Registry System: 4-CHLOROADAMANTAN-1-OL(61357-37-7)
  • 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: 61357-37-7(Hazardous Substances Data)

61357-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61357-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,5 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61357-37:
(7*6)+(6*1)+(5*3)+(4*5)+(3*7)+(2*3)+(1*7)=117
117 % 10 = 7
So 61357-37-7 is a valid CAS Registry Number.

61357-37-7Upstream product

61357-37-7Downstream Products

61357-37-7Relevant articles and documents

On the reactivity of C(sp3)-H σ-bonds: Oxygenation with methyl(trifluoromethyl)dioxirane

Mello, Rossella,Royo, Jorge,Andreu, Cecilia,Baguena-Ano, Minerva,Asensio, Gregorio,Gonzalez-Nunez, Maria Elena

, p. 455 - 466 (2008)

The reactivity of C-H σ-bonds of a series of 2-substituted adamantanes 2 towards methyl(trifluoromethyl)dioxirane (1) shows a consistent dependence on the electron-withdrawing ability, either inductive or by resonance, of the substituent. The results are

CHARGE DISPERSAL IN 1- AND 2-ADAMANTYL CATIONS

Grob, Cyril A.,Wang, Guangyi,Yang, Chengxi

, p. 1247 - 1250 (2007/10/02)

Substituents at the remoter 5-position of 2-adamantyl arylsulfonates controlsolvolysis rates more strongly than substituents the 4-position.

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