467030
1-Cyclohexene-1-carboxaldehyde
97%
동의어(들):
Δ1-Tetrahydrobenzaldehyde, 1-Cyclohexenecarboxaldehyde, 1-Cyclohexenylaldehyde, 1-Formyl-1-cyclohexene, 1-Formylcyclohexene
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
C6H9CHO
CAS Number:
Molecular Weight:
110.15
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
97%
bp
61 °C/10 mmHg (lit.)
density
0.966 g/mL at 25 °C (lit.)
SMILES string
O=CC1=CCCCC1
InChI
1S/C7H10O/c8-6-7-4-2-1-3-5-7/h4,6H,1-3,5H2
InChI key
OANSOJSBHVENEI-UHFFFAOYSA-N
일반 설명
1-Cyclohexene-1-carboxaldehyde is an α,β-unsaturated aldehyde. It participates in the synthesis of benzopyrans.
애플리케이션
1-Cyclohexene-1-carboxaldehyde may be used in the synthesis of azomethine imines.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
149.0 °F - closed cup
Flash Point (°C)
65 °C - closed cup
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
Feng Shi et al.
Tetrahedron letters, 50(28), 4067-4070 (2010-02-18)
A [3+2] 1,3-dipolar cycloaddition reaction of arynes with stable azomethine imines has been developed. The reaction rapidly assembles tricyclic pyrazoloindazolone derivatives in moderate yields under mild reaction conditions.
Efficient and general method for the synthesis of benzopyrans by ethylenediamine diacetate-catalyzed reactions of resorcinols with α, β-unsaturated aldehydes. One step synthesis of biologically active (?)-confluentin and (?)-daurichromenic acid.
Lee YR, et al.
Tetrahedron Letters, 46(44), 7539-7543 (2005)
Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6p-electrocyclization in water and application to natural products.
Jung EJ, et al.
Green Chemistry, 12(11), 2003-2011 (2010)
Yi Wang et al.
Plant, cell & environment, 44(2), 559-573 (2020-11-21)
In plants, cellular lipid peroxidation is enhanced under low nitrogen (LN) stress; this increases the lipid-derived reactive carbonyl species (RCS) levels. The cellular toxicity of RCS can be reduced by various RCS-scavenging enzymes. However, the roles of these enzymes in
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