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127583-05-5

(2R,3S)-1-Benzyloxy-3-cyclopropyl-2-hydroxy-dodecan-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127583-05-5 Structure

  • Basic information

    1. Product Name: (2R,3S)-1-Benzyloxy-3-cyclopropyl-2-hydroxy-dodecan-4-one
    2. Synonyms:
    3. CAS NO:127583-05-5
    4. Molecular Formula:
    5. Molecular Weight: 346.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127583-05-5.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: (2R,3S)-1-Benzyloxy-3-cyclopropyl-2-hydroxy-dodecan-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3S)-1-Benzyloxy-3-cyclopropyl-2-hydroxy-dodecan-4-one(127583-05-5)
    11. EPA Substance Registry System: (2R,3S)-1-Benzyloxy-3-cyclopropyl-2-hydroxy-dodecan-4-one(127583-05-5)

  • 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: 127583-05-5(Hazardous Substances Data)

127583-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127583-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,8 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 127583-05:
(8*1)+(7*2)+(6*7)+(5*5)+(4*8)+(3*3)+(2*0)+(1*5)=135
135 % 10 = 5
So 127583-05-5 is a valid CAS Registry Number.

127583-05-5Relevant articles and documents

Stereospecific 1,2-Rearrangement of Cyclopropyl Group. Synthesis of Chiral α-Cyclopropyl Ketones and α-Cyclopropyl Aldols

Shimazaki, Masato,Hara, Hisaaki,Suzuki, Keisuke

, p. 5443 - 5446 (1989)

Stereospecific 1,2-rearrangement of cyclopropyl group is described as an efficient route to stereo-defined α-cyclopropyl ketones and α-cyclopropyl aldols.Acceleration of the reaction by the introduction of trimethylsilyl(TMS) group to the α-position of cy

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