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Benzoic acid, 4,4'-[1,2-phenylenebis(methyleneoxy)]bis-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64879-83-0 Structure
  • Basic information

    1. Product Name: Benzoic acid, 4,4'-[1,2-phenylenebis(methyleneoxy)]bis-, dimethyl ester
    2. Synonyms:
    3. CAS NO:64879-83-0
    4. Molecular Formula: C24H22O6
    5. Molecular Weight: 406.435
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64879-83-0.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: Benzoic acid, 4,4'-[1,2-phenylenebis(methyleneoxy)]bis-, dimethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 4,4'-[1,2-phenylenebis(methyleneoxy)]bis-, dimethyl ester(64879-83-0)
    11. EPA Substance Registry System: Benzoic acid, 4,4'-[1,2-phenylenebis(methyleneoxy)]bis-, dimethyl ester(64879-83-0)
  • 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: 64879-83-0(Hazardous Substances Data)

64879-83-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64879-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64879-83:
(7*6)+(6*4)+(5*8)+(4*7)+(3*9)+(2*8)+(1*3)=180
180 % 10 = 0
So 64879-83-0 is a valid CAS Registry Number.

64879-83-0SDS

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 dimethyl 4,4'-((1,2-phenylenebis(methylene))bis(oxy))dibenzoate

1.2 Other means of identification

Product number -
Other names -

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:64879-83-0 SDS

64879-83-0Relevant articles and documents

Synthesis of novel carbazole based macrocyclic amides as potential antimicrobial agents

Rajakumar, Perumal,Sekar, Karuppannan,Shanmugaiah, Vellasamy,Mathivanan, Narayanasamy

scheme or table, p. 3040 - 3045 (2009/10/02)

A series of carbazole based macrocyclic diamides with thia and oxy linkages have been synthesized and the inhibitory activity of the cyclophane amides against human pathogenic bacteria and plant pathogenic fungi are documented. (S)-1,10-Bi-2-naphthol [(S)

Synthesis and complexation studies of intra annularly linked bicyclic cyclophanes

Rajakumar, Perumal,Kanagalatha, Rajagopal

, p. 9735 - 9741 (2007/10/03)

The cyclophanes derived from 2,6-bis(chloromethyl)benzoquinone and suitable dithiols were reduced with sodium dithionate and then further coupled with various dibromides to give intra annularly linked bicyclic cyclophanes, which forms charge transfer comp

Synthesis of cyclophanes with intra-annular functionality and cage structure

Kannan, Arunachalam,Rajakumar, Perumal,Kabaleeswaran,Rajan

, p. 5090 - 5102 (2007/10/03)

Cyclophanes of the type 1 and 2, with large cavity sizes, have been synthesized from the corresponding dichloride 8 or 8a and o-xylene-α,α′-dithiol (9), p-xylene-α,α′-dithiol (10), or m-terphenyldithiol (11). Similarly, cyclophanes of the type 3 with intr

Synthesis and molecular transformations of functionalised cyclophanes with large cavity

Kannan,Rajakumar

, p. 3053 - 3065 (2007/10/03)

Cyclophanes of the type 1 and 3 are obtained by the coupling of suitable dithiol with corresponding dibromide under high dilution technique in the presence of KOH in benzene or toluene-ethanol. Few molecular transformations have been effected on the cyclo

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