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CAS

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78855-52-4

(1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 78855-52-4 Structure

  • Basic information

    1. Product Name: (1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol
    2. Synonyms: (1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol
    3. CAS NO:78855-52-4
    4. Molecular Formula:
    5. Molecular Weight: 318.437
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78855-52-4.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: (1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol(78855-52-4)
    11. EPA Substance Registry System: (1R,2R,3S,4S)-2-((R)-Benzenesulfinyl)-3-methyl-1-phenyl-pentane-1,4-diol(78855-52-4)

  • 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: 78855-52-4(Hazardous Substances Data)

78855-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78855-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,5 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78855-52:
(7*7)+(6*8)+(5*8)+(4*5)+(3*5)+(2*5)+(1*2)=184
184 % 10 = 4
So 78855-52-4 is a valid CAS Registry Number.

78855-52-4Relevant articles and documents

STUDIES OF STEREOCHEMICAL CONTROL USING α-LITHIOSULFINYL CARBANIONS

Williams, David R.,Phillips, James G.,White, Franklin H.,Huffman, John C.

, p. 3003 - 3012 (2007/10/02)

The stereoselectivity in reactions of α-lithiosulfinyl carbanions with aldehydes has been unambiguously established.Steric effects and intramolecular chelation of the associated cation are important factors contributing to the observed outcome.

A Stereoselective Approach to Acyclic Systems via Condensations of α-Lithiosulfinyl Carbanions and Aldehydes

Williams, David R.,Phillips, James G.,Huffman, John C.

, p. 4101 - 4103 (2007/10/02)

The stereochemical outcome of condensations of α-lithiosulfinyl carbanions with aldehydes is presented, and demonstrates useful methodology for generating 1,2-asymmetry, as well as construction of 1,3-asymmetric relationships in acyclic systems.

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