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Merck
CN

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
Beilstein:
111928
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
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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