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CAS

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582300-87-6

5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 582300-87-6 Structure

  • Basic information

    1. Product Name: 5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE
    2. Synonyms: 5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE
    3. CAS NO:582300-87-6
    4. Molecular Formula: C14H20O8S2
    5. Molecular Weight: 380.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 582300-87-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE(582300-87-6)
    11. EPA Substance Registry System: 5,5-(DIMETHANESULFONATE)DIMETHANOL-2-PHENYL-1,3-DIOXANE(582300-87-6)

  • 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: 582300-87-6(Hazardous Substances Data)

582300-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 582300-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,2,3,0 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 582300-87:
(8*5)+(7*8)+(6*2)+(5*3)+(4*0)+(3*0)+(2*8)+(1*7)=146
146 % 10 = 6
So 582300-87-6 is a valid CAS Registry Number.

582300-87-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-(methylsulfonyloxymethyl)-2-phenyl-1,3-dioxan-5-yl]methyl methanesulfonate

1.2 Other means of identification

Product number -
Other names {5-[(methanesulfonyloxy)methyl]-2-phenyl-1,3-dioxan-5-yl}methyl methanesulfonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:582300-87-6 SDS

582300-87-6Downstream Products

582300-87-6Relevant articles and documents

ANTIOXIDANT POLYMERS CONTAINING [1,2]-DITHIOLANE MOIETIES AND USES THEREOF

-

Page/Page column 53, (2008/12/07)

The present invention describes polymers containing 1,2-dithiolanes capable of acting as scavengers of free radicals, metals and reactive oxygen species. Also described are methods of synthesizing the antioxidant 1,2-dithiolane derivatives and polymerization thereof to produce biodegradable antioxidant polymers. The antioxidant polymers of the present invention may be used to treat diseases or conditions caused by oxidative stress and other free radical mediated conditions. The antioxidant polymers may also be used for the preparation of antioxidant particulate delivery devices of therapeutic agents.

Synthesis of functionalised derivatives of pentaerythritol

Ashry, E. S. H. El,Kilany, Y. El,Hamid, H. Abdel,El-Zemity, S. R.,Boghdady, S.

, p. 111 - 128 (2007/10/03)

Ring opening of the dibenzylidene derivative of pentaerythritol 12 with N-bromosuccinimide gave di-O-benzoyldibromodideoxypentaerythritol (29). Reaction of 20 and 21 with hydrogen bromide in acetic acid afforded di-O-acetyl-di-O-p-toluenesulfonyl pentaerythritol (26). Nucleophilic displacement of the tosyloxy groups in 20 by 1,2,4 triazole afforded 2-phenyl-5-(p-toluenesulfonyloxymethyl)-5-(1,2,4-triazolylmethyl)-1,3-dioxan (31) and 2-phenyl-5,5-bis(1,2,4-triazolylmethyl)-1,3-dioxan (32), and with benzotriazole gave 2-phenyl-5,5-bis(benzotriazolylmethyl)-1,3-dioxan (30). The activity of various derivatives against hepatitis B virus has been studied.

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