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4-Cholestene-3α,19-diol 3-Acetate 19-p-Toluenesulphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115884-04-3 Structure
  • Basic information

    1. Product Name: 4-Cholestene-3α,19-diol 3-Acetate 19-p-Toluenesulphonate
    2. Synonyms:
    3. CAS NO:115884-04-3
    4. Molecular Formula:
    5. Molecular Weight: 598.888
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115884-04-3.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: 4-Cholestene-3α,19-diol 3-Acetate 19-p-Toluenesulphonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Cholestene-3α,19-diol 3-Acetate 19-p-Toluenesulphonate(115884-04-3)
    11. EPA Substance Registry System: 4-Cholestene-3α,19-diol 3-Acetate 19-p-Toluenesulphonate(115884-04-3)
  • 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: 115884-04-3(Hazardous Substances Data)

115884-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115884-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,8 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 115884-04:
(8*1)+(7*1)+(6*5)+(5*8)+(4*8)+(3*4)+(2*0)+(1*4)=133
133 % 10 = 3
So 115884-04-3 is a valid CAS Registry Number.

115884-04-3Downstream Products

115884-04-3Relevant articles and documents

SOLVOLYTIC REARRANGEMENTS IN 4β,5-CYCLOPROPANO-5β-CHOLESTANE-3β,19-DIOL 3-ACETATE 19-p-TOLUENESULPHONATE

Joska, Jiri,Fajkos, Jan,Turecek, Frantisek

, p. 2991 - 3012 (2007/10/02)

Acetolysis of the tosylate VIII proceeded under participation of the cyclopropane ring at the electron-deficient center formed during the reaction to yield three products all having modified steroid skeletons.They were the diene XXIII, the unsaturated acetate XI, and the saturated 4β,10β-cycloderivative XIII carrying two acetoxy groups in the molecule.For the purpose of spectral studies and structure elucidation the acetolysis has been carried out with the labelled tosylate XXXII the synthesis of which is described and analogous three labelled products were isolated.The structures of these products were established on the basis of spectral and chemical evidence and a mechanism of the rearrangements is proposed.

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