183962
2,3-二氢苯并呋喃
99%
别名:
氯杀鼠灵
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关于此项目
经验公式（希尔记法）:
C8H8O
化学文摘社编号:
分子量:
120.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-817-3
Beilstein/REAXYS Number:
111928
MDL number:
Assay:
99%
Form:
liquid
refractive index
n20/D 1.549 (lit.)
bp
188-189 °C (lit.)
solubility
alcohol: soluble, carbon disulfide: soluble, chloroform: soluble, diethyl ether: soluble
density
1.065 g/mL at 25 °C (lit.)
InChI key
HBEDSQVIWPRPAY-UHFFFAOYSA-N
InChI
1S/C8H8O/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H2
SMILES string
C1Cc2ccccc2O1
assay
99%
form
liquid
Quality Level
Gene Information
human ... CYP1A2(1544)
General description
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。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
152.6 °F - closed cup
flash_point_c
67 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
J Malmström et al.
Journal of the American Chemical Society, 123(15), 3434-3440 (2001-07-27)
A novel synthesis of 2,3-dihydrobenzo[b]thiophene-5-ol based on intramolecular homolytic substitution on sulfur was reported. The "antioxidant profile" of the series of 2,3-dihydrobenzo[b]furan-5-ol (2a) its 1-thio (2b), 1-seleno (2c) and 1-telluro (2d) analogues was determined by studies of redox properties, the
Xiangtai Meng et al.
Organic letters, 11(1), 137-140 (2008-12-05)
A new bifunctional phosphine catalyst, (2'-hydroxy-biphenyl-2-yl)-diethylphosphane (LBBA-1), was developed for the highly stereoselective synthesis of cis-2,3-dihydrobenzofurans via an aza-Morita-Baylis-Hillman/umpolung addition domino reaction of salicyl N-thiophosphinyl imines with electron-deficient allenes. Dual activation of both nucleophile and electrophile by the bifunctional catalyst
Structures and stereochemical assignments of some novel chiral synthons derived from the biotransformation of 2, 3-dihydrobenzofuran and benzofuran by Pseudomonas putida.
Boyd DR, et al.
Tetrahedron Asymmetry, 4(6), 1307-1324 (1993)
Guo-Hua Chu et al.
Bioorganic & medicinal chemistry letters, 15(23), 5114-5119 (2005-10-06)
Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor.
Catalytic hydrodeoxygenation of benzofuran and o-ethylphenol.
Lee C-L and Ollis DF.
J. Catal., 87(2), 325-331 (1984)
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