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6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 31021-03-1 Structure
  • Basic information

    1. Product Name: 6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone
    2. Synonyms: 6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone
    3. CAS NO:31021-03-1
    4. Molecular Formula:
    5. Molecular Weight: 276.378
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31021-03-1.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: 6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone(31021-03-1)
    11. EPA Substance Registry System: 6E-2-phenylmethyl-6-phenylmethylene-cyclohexanone(31021-03-1)
  • 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: 31021-03-1(Hazardous Substances Data)

31021-03-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31021-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,0,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31021-03:
(7*3)+(6*1)+(5*0)+(4*2)+(3*1)+(2*0)+(1*3)=41
41 % 10 = 1
So 31021-03-1 is a valid CAS Registry Number.

31021-03-1Downstream Products

31021-03-1Relevant articles and documents

A tertiary amine as a hydride donor: Trichlorosilyl triflate-mediated conjugate reduction of unsaturated ketones

Kotani, Shunsuke,Osakama, Kazuki,Sugiura, Masaharu,Nakajima, Makoto

, p. 3968 - 3971 (2011)

Bulky tertiary amines, especially dicyclohexylisobutylamine, smoothly reduced α,β-unsaturated ketones in the presence of trichlorosilyl triflate to give the corresponding saturated ketones in excellent yields. Isotope-labeling studies revealed that an α-hydrogen of the amine was transferred to the enones during reduction.

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