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1005-96-5

2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide is a complex organic compound with the chemical formula C4H11O5P. It is a cyclic phosphorus-containing molecule, specifically a 1,3,2-dioxaphosphorinane derivative, which features a phosphorus atom bonded to two oxygen atoms and a five-membered ring consisting of two carbon atoms, one oxygen atom, and two phosphorus atoms. The 2-methoxy group is attached to the carbon atom at position 2, while the 5,5-dimethyl groups are located at the carbon atoms at position .5 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide is known for its potential applications in organic synthesis and as a reagent in various chemical reactions. It is also characterized by its stability and unique reactivity due to the presence of the phosphorus atom and the氧-containing functional groups.

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  • 1005-96-5 Structure

  • Basic information

    1. Product Name: 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide
    2. Synonyms: 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide
    3. CAS NO:1005-96-5
    4. Molecular Formula: C6H13O4P
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1005-96-5.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: 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide(1005-96-5)
    11. EPA Substance Registry System: 2-Methoxy-5,5-dimethyl-1,3,2-dioxaphosphorinane 2-oxide(1005-96-5)

  • 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: 1005-96-5(Hazardous Substances Data)

1005-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1005-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1005-96:
(6*1)+(5*0)+(4*0)+(3*5)+(2*9)+(1*6)=45
45 % 10 = 5
So 1005-96-5 is a valid CAS Registry Number.

1005-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxy-5,5-dimethyl-1,3,2λ<sup>5</sup>-dioxaphosphinane 2-oxide

1.2 Other means of identification

Product number -
Other names 1,3,2-Dioxaphosphorinane,2-methoxy-5,5-dimethyl-,2-oxide

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:1005-96-5 SDS

1005-96-5Downstream Products

1005-96-5Relevant articles and documents

Phosphorochloridates from phosphorohydrazides with ButOCl: Stereospecificity, selectivity and phosphorylium ion intermediates

Harger, Martin J.P

, p. 6749 - 6752 (2007/10/03)

The efficiency with which a six-membered cyclic phosphorochloridate can be obtained from the corresponding hydrazide with retention of configuration at phosphorus, using tert-butyl hypochlorite in tert-butyl alcohol, depends on how stereoelectronic factors influence the fate of an intermediate chloride-phosphorylium ion pair.

Organophosphorus Antioxidants. X. The Hydroperoxide Decomposing Action of Phosphites, Phosphonites and Thiophosphites

Koenig, T.,Habicher, W. D.,Schwetlick, K.

, p. 913 - 922 (2007/10/02)

The kinetics and mechanism of reactions of phosphites, phosphonites, thiophosphites and hydrogenphosphites with cumyl (CHP), t-butyl (TBHP) and α-tetralyl (THP) hydrogenperoxides has been studied by means of (31)P-n.m.r. spectroscopy, high performance liquid chromatography and iodometric titration.All three valent phosphorus compounds studied initially react with hydroperoxides stoichiometrically to give the corresponding P=O products and alcohol.Some species are able to decompose cumyl hydroperoxide catalytically to form phenol and aceton.Acyloin phosphites decompose CHP catalytically after a stoichiometric reaction as thiophosphites do.Tetramethylpiperidinyl phosphites ("HALS-phosphites") react with hydroperoxides only stoichiometrically but with high velocity.Phosphonites react with hydroperoxides in the same way as the corresponding phosphites.Their reactivity, however, is much higher.Hydrogenphosphites are less reactive than phosphites in the reaction with hydroperoxides.They are able to act catalytically.

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