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Merck
CN

183962

Sigma-Aldrich

2,3-二氢苯并呋喃

99%

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别名:
氯杀鼠灵
经验公式(希尔记法):
C8H8O
CAS号:
分子量:
120.15
Beilstein:
111928
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

liquid

折射率

n20/D 1.549 (lit.)

bp

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

WGK

WGK 3

闪点(°F)

152.6 °F

闪点(°C)

67 °C

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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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
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
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.
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

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