추천 제품
vapor pressure
269 mmHg ( 37.7 °C)
Quality Level
분석
98%
형태
liquid
포함
100 ppm BHT as stabilizer
refractive index
n20/D 1.438 (lit.)
bp
68-69 °C (lit.)
mp
−76 °C (lit.)
density
0.726 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
CC(=C)C(C)=C
InChI
1S/C6H10/c1-5(2)6(3)4/h1,3H2,2,4H3
InChI key
SDJHPPZKZZWAKF-UHFFFAOYSA-N
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일반 설명
2,3-Dimethyl-1,3-butadiene (DMBD) is a conjugated diene. It undergoes Diels Alder cycloaddition reaction with 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions. It undergoes thermal [4+2] cycloaddition reaction with 3-acetyl-, 3-carbamoyl and 3-ethoxycarbonylcoumarins under solvent free conditions. DMBD participates in polymerization reactions in the presence of iron dichloride complexes based catalysts.
애플리케이션
2,3-Dimethyl-1,3-butadiene was used to investigate the reactions of 1,3-dienes with the Si(001) surface using scanning tunneling microscopy and fourier transform infrared spectroscopy.
It may be used in the following processes:
It may be used in the following processes:
- Preparation of 1,3,6-triene derivatives of corresponding 1-aryl-substituted 1,3-dienes by 1,4-hydrobutadienylation in the presence of cobalt catalyst.
- Synthesis of 6-aryl(hetaryl)-3,4-dimethyl-1-nitro-1-cyano-3-cyclohexenes by reacting with gem-cyanonitroethenes.
- As a halogen trap during the study of the photolysis reaction of dibromo adduct of 2,5-diphenyltellurophene.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
30.2 °F - closed cup
Flash Point (°C)
-1 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Cycloaddition chemistry of 1, 3-dienes on the silicon (001) surface: Competition between [4+ 2] and [2+ 2] reactions.
The Journal of Physical Chemistry B, 102(35), 6873-6879 (1998)
Efficient halogen photoelimination from dibromo, dichloro and difluoro tellurophenes.
Dalton Transactions, 44(5), 2092-2096 (2015)
Aryl (hetaryl)-containing gem-cyanonitroethenes: Synthesis, structure, and reactions with 2,3-dimethyl-1,3-butadiene.
Russ. J. Gen. Chem., 85(8), 1845-1854 (2015)
Organic & biomolecular chemistry, 8(24), 5602-5613 (2010-10-12)
The Diels-Alder cycloadditions of cyclopentadiene and 2,3-dimethyl-1,3-butadiene to a range of 2-thio-3-chloroacrylamides under thermal, catalytic and microwave conditions is described. The influence of reaction conditions on the outcome of the cycloadditions, in particular the stereoselectivity and reaction efficiency, is discussed.
Polymerization of 1, 3-dienes with iron complexes based catalysts: Influence of the ligand on catalyst activity and stereospecificity.
J. Mol. Catal. A: Chem., 204, 287-293 (2003)
문서
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. It is also referred to as a cycloaddition.
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