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3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid is a complex organic compound with the molecular formula C11H24O5Si2. It is characterized by a propanoic acid backbone, which is substituted with a unique silicon-containing moiety. The molecule features a 2-carboxyethyl-dimethyl-silyl group attached to the third carbon of the propanoic acid chain, which in turn is connected to another dimethyl-silyl group through an oxygen atom. This structure endows the compound with properties that may be of interest in various chemical applications, such as in the synthesis of silane coupling agents or as a component in materials science. The compound's specific arrangement of atoms and functional groups can influence its reactivity and compatibility with other chemicals, making it a potentially valuable building block in the creation of new materials or chemical intermediates.

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  • 4608-02-0 Structure
  • Basic information

    1. Product Name: 3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid
    2. Synonyms: 3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid
    3. CAS NO:4608-02-0
    4. Molecular Formula: C10H22O5Si2
    5. Molecular Weight: 278.4497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4608-02-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 333.1°Cat760mmHg
    3. Flash Point: 155.2°C
    4. Appearance: /
    5. Density: 1.068g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid(4608-02-0)
    11. EPA Substance Registry System: 3-[(2-carboxyethyl-dimethyl-silyl)oxy-dimethyl-silyl]propanoic acid(4608-02-0)
  • 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: 4608-02-0(Hazardous Substances Data)

4608-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4608-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4608-02:
(6*4)+(5*6)+(4*0)+(3*8)+(2*0)+(1*2)=80
80 % 10 = 0
So 4608-02-0 is a valid CAS Registry Number.

4608-02-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[2-carboxyethyl(dimethyl)silyl]oxy-dimethylsilyl]propanoic acid

1.2 Other means of identification

Product number -
Other names 3,3'-(1,1,3,3-tetramethyldisiloxane-1,3-diyl)dipropanoic acid

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:4608-02-0 SDS

4608-02-0Downstream Products

4608-02-0Relevant articles and documents

METHOD FOR THE PRODUCTION OF ORGANOSILICON COMPOUNDS COMPRISING CARBOXY RADICALS

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Page/Page column 29-30, (2008/06/13)

The invention relates to a method for the production of organosilicon compounds (2) comprising carbonyl radicals by oxidation of organosilicion compounds (1) comprising carbinol radicals with the aid of a mediator (3) selected from a group of aliphatic, cycloaliphatic, heterocyclic and aromatic NO-, NOH- and (I)-containing compounds and an oxidizing agent (4) under the proviso that the reaction is carried out with constant control of the pH value at a pH = 3 and the carbonyl radicals in the organosilicon compounds (1) thus used are oxidized to form predominantly carboxy radicals.

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