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(5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127891-07-0 Structure
  • Basic information

    1. Product Name: (5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene
    2. Synonyms: (5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene
    3. CAS NO:127891-07-0
    4. Molecular Formula:
    5. Molecular Weight: 278.176
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127891-07-0.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: (5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene(127891-07-0)
    11. EPA Substance Registry System: (5R,6S)-6-(2-Iodo-ethyl)-1,5,6-trimethyl-cyclohexene(127891-07-0)
  • 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: 127891-07-0(Hazardous Substances Data)

127891-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127891-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,8,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127891-07:
(8*1)+(7*2)+(6*7)+(5*8)+(4*9)+(3*1)+(2*0)+(1*7)=150
150 % 10 = 0
So 127891-07-0 is a valid CAS Registry Number.

127891-07-0Relevant articles and documents

Synthetic studies on neomarinone: practical and efficient stereoselective synthesis of the side chain

Suárez, Rosa M.,Montserrat Martínez,Sarandeses, Luis A.,Pérez Sestelo, José

, p. 6493 - 6495 (2007)

A practical and efficient stereoselective synthesis of the side chain of neomarinone is reported. The synthesis was achieved in six steps (41% overall yield) from 2-methyl-2-cyclohexenone. The key step is a novel stereoselective 1,4-conjugate addition/eno

TOTAL SYNTHESIS OF (+/-)-AGELINE A, A PHYSIOLOGICALLY ACTIVE CONSTITUENT OF AGELAS SPONGES

Asao, Kazuhiko,Iio, Hideo,Tokoroyama, Takashi

, p. 6401 - 6404 (2007/10/02)

The monocyclic diterpene moiety of ageline A (1) was convergently constructed by the palladium-mediated coupling of C9-terpenic chain as vinyl bromide 10 and C11-monocyclic segment as alkylzinc compound 16, which was obtained through a stereoselective cyc

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