Basic information Safety Supplier Related

2,3-Dimethoxy-1,3-butadiene

Basic information Safety Supplier Related

2,3-Dimethoxy-1,3-butadiene Basic information

Product Name:
2,3-Dimethoxy-1,3-butadiene
Synonyms:
  • 2,3-Dimethoxy-buta-1,3-Diene
  • 2,3-DIMETHOXY-1,3-BUTADIENCE
  • 2,3-DIMETHOLXY-1,3-BUTADIENE
  • 2,3-Dimethoxy-1,3-butadiene 95%
  • 2,3-Dimethoxy-1,3-bu
  • 2,3-DIMETHOXY-1,3-BUTADIENE
  • 1,3-Butadiene, 2,3-dimethoxy-
  • Aminocaproic acid impurities3
CAS:
3588-31-6
MF:
C6H10O2
MW:
114.14
Product Categories:
  • Enol Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Building Blocks
  • Chemical Synthesis
  • Enol Ethers
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
3588-31-6.mol
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2,3-Dimethoxy-1,3-butadiene Chemical Properties

Melting point:
19 °C (lit.)
Boiling point:
134-136 °C/745 mmHg (lit.)
Density 
0.94 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.459(lit.)
Flash point:
91 °F
storage temp. 
2-8°C
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Safety Information

Risk Statements 
10
Safety Statements 
16-33
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
HazardClass 
3.2
PackingGroup 
III

MSDS

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2,3-Dimethoxy-1,3-butadiene Usage And Synthesis

Uses

2,3-Dimethoxy-1,3-butadiene has been employed as diene to investigate the Diels-Alder chemistry of pristine and defective graphene. It was also used in the synthesis of novel benzopentathiepin varacinium trifluoroacetate.
It may be used in the preparation of 3,4-dimethoxythiophene, an intermediate for the synthesis of 3,4-ethylenedioxythiophene (EDOT). It may also be used to form thio esters by reacting with mercaptans in the presence of cobalt carbonyl catalyst.

General Description

2,3-Dimethoxy-1,3-butadiene (DMEBD) is a 1,3-butadiene derivative. The reaction kinetics of hydrolysis of 2,3-dimethoxy-1,3-butadiene in the presence of acid catalyst has been investigated. The [4+2] cycloadditions of 3-nitrocoumarins with DMEBD has been investigated in aqueous medium, in organic solvent and under solventless conditions. This reaction led to the formation of 4-substituted 3-nitrochromanones. It forms adducts with graphene and Diels-Alder chemistry in this formation has been investigated.

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