추천 제품
분석
98%
형태
liquid
refractive index
n20/D 1.469 (lit.)
bp
86-87 °C/12 mmHg (lit.)
mp
4-5 °C (lit.)
density
1.185 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
O=C1OCC=C1
InChI
1S/C4H4O2/c5-4-2-1-3-6-4/h1-2H,3H2
InChI key
VIHAEDVKXSOUAT-UHFFFAOYSA-N
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일반 설명
Chiral urea compounds catalyzed hetero-Michael addition reaction of 2(5H)-furanone (γ-crotonolactone) to pyrrolidine. The quorum sensing inhibition activity by 2(5H)-furanone was studied using bioindicator strains.
애플리케이션
2(5H)-Furanone (γ-Crotonolactone) has been used in:
- synthesis of (+)-L-733,060, (+)-CP-99,994 and (2S,3R)-3-hydroxypipecolic acid
- synthesis of 5-substituted 2(5H) furanones (γ-butenolides) via direct aldol reaction with aromatic aldehydes catalyzed by bifunctional aminothiourea and aminosquaramide organocatalysts
- Michael addition reactions for synthesis of lignans
- three-component Michael-Aldol reactions with an aldehyde anda thiolate or carbanion
포장
Bottomless glass bottle. Contents are inside inserted fused cone.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
213.8 °F - closed cup
Flash Point (°C)
101 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Tetrahedron, 49, 9039-9039 (1993)
Tetrahedron, 49, 8073-8073 (1993)
Tetrahedron, 49, 4173-4173 (1993)
ACS synthetic biology, 9(8), 2107-2118 (2020-08-14)
Strigolactones are plant hormones and rhizosphere signaling molecules with key roles in plant development, mycorrhizal fungal symbioses, and plant parasitism. Currently, sensitive, specific, and high-throughput methods of detecting strigolactones are limited. Here, we developed genetically encoded fluorescent strigolactone biosensors based
Chemical & pharmaceutical bulletin, 52(4), 477-480 (2004-04-02)
Chiral urea compounds 10a-g were synthesized as catalysts for conjugate addition of pyrrolidine (2) to gamma-crotonolactone (3). In the presence of a catalytic amount of the chiral ureas, this hetero-Michael reaction was greatly accelerated. Asymmetric induction was observed with the
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