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质量水平
方案
99%
表单
liquid
折射率
n20/D 1.549 (lit.)
沸点
188-189 °C (lit.)
溶解性
alcohol: soluble
carbon disulfide: soluble
chloroform: soluble
diethyl ether: soluble
密度
1.065 g/mL at 25 °C (lit.)
SMILES字符串
C1Cc2ccccc2O1
InChI
1S/C8H8O/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H2
InChI key
HBEDSQVIWPRPAY-UHFFFAOYSA-N
基因信息
human ... CYP1A2(1544)
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一般描述
已经研究了使用恶臭假单胞菌 UV4 的完整细胞生物转化 2，3-二氢苯并呋喃。2，3-二氢苯并呋喃是在苯并呋喃的催化加氢脱氧过程中形成的中间体。
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
152.6 °F - closed cup
闪点(°C)
67 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
H S Heine et al.
Chemico-biological interactions, 59(2), 219-230 (1986-09-01)
The effects of dietary administration of equimolar doses (5 mmol/kg body wt per day) of trimethylene oxide, trimethylene sulfide, coumaran, benzofuran, indole, and indole-3-carbinol on the activities of microsomal epoxide hydrolase and several other xenobiotic metabolizing enzymes were measured in
Leticia Jiménez-González et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(34), 8762-8769 (2006-09-06)
2,3-Dihydrobenzofurans can be diastereoselectively prepared by condensation of aromatic aldehydes with 2,3-dihydrobenzoxasilepines under the catalysis of Ag(I) complexes, and in the presence of a source of fluoride ion. The application of this strategy by using chiral catalysts leads to a
S Antus et al.
Chirality, 13(8), 493-506 (2001-07-24)
The correlation between the helicity (absolute conformation) of the O-heterocyclic ring of chiral 2,3-dihydrobenzo[b]furan (1) and chromane (2) derivatives and their (1)L(b) band CD was investigated. The same helicity rule was found for both unsubstituted chromophores: P/M helicity of the
S Ohkawa et al.
Journal of medicinal chemistry, 40(4), 559-573 (1997-02-14)
A series of 2,3-dihydro-5-benzofuranamines (5-aminocoumarans) were developed for the treatment of traumatic and ischemic central nervous system (CNS) injury. Compounds within this class were extremely effective inhibitors of lipid peroxidation in vitro and antagonized excitatory behavior coupled with peroxidative injury
Prashant P Deshpande et al.
Journal of industrial microbiology & biotechnology, 35(8), 901-906 (2008-05-23)
Microbial hydroxylation of o-bromophenylacetic acid provided 2-bromo-5-hydroxyphenylacetic acid. This enabled a route to the key intermediate 4-bromo-2,3-dihydrobenzofuran for synthesizing a melatonin receptor agonist and sodium hydrogen exchange compounds. Pd-mediated coupling reactions of 4-bromo-2,3-dihydrobenzofuran provided easy access to the 4-substituted-2,3-dihydrobenzofurans.
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