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CAS

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133464-07-0

(R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133464-07-0 Structure

  • Basic information

    1. Product Name: (R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide
    2. Synonyms: (R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide
    3. CAS NO:133464-07-0
    4. Molecular Formula:
    5. Molecular Weight: 190.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133464-07-0.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: (R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide(133464-07-0)
    11. EPA Substance Registry System: (R)-4-Cyclohexyl-[1,3,2]dioxathiolane 2-oxide(133464-07-0)

  • 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: 133464-07-0(Hazardous Substances Data)

133464-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 133464-07-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133464-07:
(8*1)+(7*3)+(6*3)+(5*4)+(4*6)+(3*4)+(2*0)+(1*7)=110
110 % 10 = 0
So 133464-07-0 is a valid CAS Registry Number.

133464-07-0Relevant articles and documents

Synthesis of Homochiral Amino Alcohols, Aziridines and Diamines via Homochiral Cyclic Sulphites

Lohray, Braj B.,Ahuja, Jaimala R.

, p. 95 - 97 (1991)

Vicinal diols react with thionyl chloride to give 1,2-cyclic sulphites in quantitative yield, which undergo facile ring opening by lithium azide in dimethylformamide to yield azido alcohols and the latter in turn have been stereoselectively transformed into amino alcohols, aziridines and diamines.

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