추천 제품
Quality Level
분석
96%
양식
liquid
포함
sodium bicarbonate as stabilizer
refractive index
n20/D 1.479 (lit.)
bp
68-70 °C/8 mmHg (lit.)
density
1.542 g/mL at 25 °C (lit.)
작용기
bromo
ether
저장 온도
2-8°C
SMILES string
BrCCC1OCCO1
InChI
1S/C5H9BrO2/c6-2-1-5-7-3-4-8-5/h5H,1-4H2
InChI key
GGZQLTVZPOGLCC-UHFFFAOYSA-N
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관련 카테고리
일반 설명
Copper-catalyzed borylation of 2-(2-bromoethyl)-1,3-dioxolane with bis(pinacolato)diboron followed by treatment with potassium bifluoride affords the key organotrifluoroborate reagent.
2-(2-Bromoethyl)-1,3-dioxolane is a cyclic ether derivative with a dioxolane ring, used as a building block in organic synthesis and polymer industry.
2-(2-Bromoethyl)-1,3-dioxolane is a cyclic ether derivative with a dioxolane ring, used as a building block in organic synthesis and polymer industry.
애플리케이션
2-(2-Bromoethyl)-1,3-dioxolane was used:
- as starting reagent for the synthesis of (5Z,9Z)-5,9-hexadecadienoic acid, (5Z,9Z)-5,9-nonadecadienoic acid and (5Z,9Z)-5,9-eicosadienoic acid
- in synthesis of 1-deoxy-castanospermine and 1-deoxy-8a-epi-castanospermine
- in asymmetric total synthesis of both enantiomers of marine mollusk metabolite pulo′upone via Evans′ asymmetric Diels-Alder reaction
- as alkylating agent for amines, dithianes and carboximides
- with eynamides and sodium azide in a "one-pot" synthesis of triazoles
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point (°F)
149.0 °F - closed cup
Flash Point (°C)
65 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Tetrahedron Letters, 34, 6411-6411 (1993)
Journal of the Chemical Society. Perkin Transactions 1, 681-681 (1993)
Chemistry and physics of lipids, 100(1-2), 33-40 (2000-01-20)
The delta 5,9 fatty acids (5Z,9Z)-5,9-hexadecadienoic acid, (5Z,9Z)-5,9-nonadecadienoic acid, and (5Z,9Z)-5,9-eicosadienoic acid were synthesized for the first time in four steps (9-12% overall yield) starting from commercially available 2-(2-bromoethyl)-1,3-dioxolane. The synthetic approach provided enough material to corroborate the structure and
Tetrahedron Letters, 34, 7705-7705 (1993)
Advanced Synthesis & Catalysis, 348, 2437-2437 (2006)
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