Epoxy curing agent Knowledge 2,3,4-Trimethoxybenzoic acid

2,3,4-Trimethoxybenzoic acid

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2,3,4-trimethoxybenzoic acid structural formula

Structural formula

Business number 05U8
Molecular formula C10H12O5
Molecular weight 212.2
label

2,3,4-Trimethoxybenzoic acid,

Benzoic acid 2,3,4-trimethoxy-,

2,3,4-Trimethoxybenzoic,

aromatic compounds

Numbering system

CAS number:573-11-5

MDL number:MFCD00002433

EINECS number:209-350-0

RTECS number:None

BRN number:2696073

PubChem number:24851397

Physical property data

1. Physical property data


1. Character: white or off-white crystal


2. Melting point (): 99-102

Toxicological data

None yet

Ecological data

3. Ecological data:


1, other harmful effects: This substance may be harmful to the environment, special attention should be paid to water bodies.

Molecular structure data


5. Molecular property data:


1. Molar refractive index: 53.21


2. Molar volume (m3/mol):173.9


3. isotonic specific volume (90.2K):439.4


4. Surface Tension (dyne/cm):40.6


5. Polarizability10-24cm3):21.09

Compute chemical data

4. Calculated chemical data:


1. Hydrophobic parameters Calculate reference value (XlogP):1.7


2. Hydrogen Bonding Number of donors: 1


3. Hydrogen Bonding Number of receptors: 5


4. Rotatable Number of chemical bonds: 4


5. Topological molecules Polar surface area (TPSA):65


6. Heavy atoms Quantity: 15


7. Surface charge :0


8. Complexity :218


9. Isotope atomic number:0


10. Determine the number of atomic stereocenters:0


11. Uncertain number of atomic stereocenters:0


12. Determine the number of stereocenters of chemical bonds:0


13. Uncertain number of chemical bond stereocenters:0


14. Number of covalent bond units: 1

Properties and stability

Stability and reactivity:


Materials to avoid: Oxides.


Products to be decomposed: carbon monoxide and carbon dioxide.

Storage method

Storage:


Seal the secret container and store it in a sealed main container in a cool place Dry position.

Synthesis method

None yet

Purpose

Purpose:


Used as an intermediate in organic synthesis.

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