ChemicalBook > CAS DataBase List > 2,5-DIMETHOXYTEREPHTHALALDEHYDE

2,5-DIMETHOXYTEREPHTHALALDEHYDE

Product Name
2,5-DIMETHOXYTEREPHTHALALDEHYDE
CAS No.
7310-97-6
Chemical Name
2,5-DIMETHOXYTEREPHTHALALDEHYDE
Synonyms
LABOTEST-BB LT00137779;3,6-Dimethoxyterephthalaldehyde;2,5-DIMETHOXYTEREPHTHALALDEHYDE;2,5-DIMETHOXY-1,4-DICARBOXALDEHYDE;2,5-Dimethoxybenzene-1,4-dicarbaldehyde;2,5-DIMETHOXYBENZENE-1,4-DICARBOXALDEHYDE;2,5-Dimethoxy-1,4-benzenedicarboxaldehyde;2,5-Dimethoxy-1,4-benzenedicarboxaldehyde ;1,4-Benzenedicarboxaldehyde, 2,5-dimethoxy-;2,5-Dimethoxybenzene-1,4-dicarboxaldehyde 97%
CBNumber
CB5414709
Molecular Formula
C10H10O4
Formula Weight
194.18
MOL File
7310-97-6.mol
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2,5-DIMETHOXYTEREPHTHALALDEHYDE Property

Melting point:
209-213 °C
Boiling point:
371℃
Density 
1.207
Flash point:
168℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
Light yellow to yellow
InChI
InChI=1S/C10H10O4/c1-13-9-3-8(6-12)10(14-2)4-7(9)5-11/h3-6H,1-2H3
InChIKey
YSIIHTHHMPYKFP-UHFFFAOYSA-N
SMILES
C1(C=O)=CC(OC)=C(C=O)C=C1OC
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
2912490090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
715026
Product name
2,5-Dimethoxybenzene-1,4-dicarboxaldehyde
Purity
97%
Packaging
1g
Price
$138
Updated
2025/07/31
TCI Chemical
Product number
D6056
Product name
2,5-Dimethoxyterephthalaldehyde
Purity
min. 98.0 %
Packaging
1G
Price
$79
Updated
2025/07/31
TCI Chemical
Product number
D6056
Product name
2,5-Dimethoxyterephthalaldehyde
Purity
min. 98.0 %
Packaging
5G
Price
$237
Updated
2025/07/31
TRC
Product number
B429625
Product name
2,5-dimethoxyterephthalaldehyde
Packaging
20mg
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FD66165
Product name
2,5-Dimethoxyterephthalaldehyde
Packaging
250mg
Price
$95
Updated
2021/12/16
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2,5-DIMETHOXYTEREPHTHALALDEHYDE Chemical Properties,Usage,Production

Uses

1. Synthesis of bis(N-salicylidene-aniline)s BSANs 2. COF applications

Synthesis

3752-97-4

7310-97-6

1. To a solution of 1,4-dimethoxybenzene (10.0 g, 72.3 mmol) in 1,4-dioxane (30 mL), 38% aqueous formaldehyde (5 mL) and paraformaldehyde (3.0 g, 99.0 mmol) were added sequentially. The reaction mixture was heated to 90°C and concentrated hydrochloric acid (5 mL each) was added in two portions over 30 minutes. The reaction mixture was continued to be heated for 1 hour and then 30 mL of concentrated hydrochloric acid was added. Cooled to room temperature, a white precipitate was precipitated, collected by filtration and dried under vacuum. The crude product was recrystallized from acetone to give 1,4-bis(chloromethyl)-2,5-dimethoxybenzene (4.5 g, 26% yield) as a white solid. 2. 1,4-bis(chloromethyl)-2,5-dimethoxybenzene (15.0 g, 63.8 mmol) and hexamethylenetetetramine (18.0 g, 127.6 mmol) were dissolved in chloroform (50 mL) and refluxed and stirred for 24 hours. After the reaction was completed, it was cooled to room temperature and the light yellow precipitate was collected by filtration. The precipitate was dissolved in water (30 mL), acidified by the addition of acetic acid (10 mL) and stirred at 90 °C for 24 hours. After cooling to room temperature, it was extracted with dichloromethane (200 mL). The organic phase was washed three times with water (200 mL) and dried over anhydrous sodium sulfate. After evaporating the solvent, the residue was recrystallized from ethanol to give 2,5-dimethoxybenzene-1,4-dicarboxaldehyde (5.5 g, 45% yield) as a bright yellow solid. 1H NMR (300 MHz, CDCl3) δ 10.50 (s, 2H), 7.26 (s, 2H), 3.95 (s, 6H). 13C NMR (101 MHz, CDCl3) δ 189.19, 155.73, 129.15, 110.92, 77.33, 77.01, 76.70, 56.23. FTMS for C10H10O4: calcd. m/z 195.1 [M + 1]+; found 194.1.

References

[1] Bulletin of the Korean Chemical Society, 2010, vol. 31, # 10, p. 2755 - 2756
[2] Science China Chemistry, 2018, vol. 61, # 7, p. 857 - 862
[3] Journal of the American Chemical Society, 2018, vol. 140, # 3, p. 984 - 992
[4] Journal of Molecular Structure, 2016, vol. 1106, p. 121 - 129
[5] Journal of the American Chemical Society, 1950, vol. 72, p. 2992

2,5-DIMETHOXYTEREPHTHALALDEHYDE Preparation Products And Raw materials

Raw materials

Preparation Products

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2,5-DIMETHOXYTEREPHTHALALDEHYDE Suppliers

Alfa Chemistry
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View Lastest Price from 2,5-DIMETHOXYTEREPHTHALALDEHYDE manufacturers

ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
Product
2,5-Dimethoxybenzene-1,4-dicarboxaldehyde 7310-97-6
Price
US $3.00-9.00/KG
Min. Order
0.1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2025-06-25
WUHAN FORTUNA CHEMICAL CO., LTD
Product
2,5-Dimethoxyterephthalaldehyde 7310-97-6
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-02-22
Capot Chemical Co.,Ltd.
Product
2,5-Dimethoxyterephthalaldehyde 7310-97-6
Price
US $0.00-0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
kgs
Release date
2023-01-03

7310-97-6, 2,5-DIMETHOXYTEREPHTHALALDEHYDERelated Search:


  • 2,5-DIMETHOXYTEREPHTHALALDEHYDE
  • 2,5-DIMETHOXY-1,4-DICARBOXALDEHYDE
  • 2,5-Dimethoxybenzene-1,4-dicarbaldehyde
  • 2,5-DIMETHOXYBENZENE-1,4-DICARBOXALDEHYDE
  • LABOTEST-BB LT00137779
  • 2,5-Dimethoxy-1,4-benzenedicarboxaldehyde
  • 2,5-Dimethoxy-1,4-benzenedicarboxaldehyde
  • 2,5-Dimethoxybenzene-1,4-dicarboxaldehyde 97%
  • 1,4-Benzenedicarboxaldehyde, 2,5-dimethoxy-
  • 3,6-Dimethoxyterephthalaldehyde
  • 7310-97-6
  • 7310-97-0
  • Aromatic Aldehydes & Derivatives (substituted)