13161-32-5 (4-羟基异苯并呋喃-1(3h)-酮,4-hydroxy-1(3H)-Isobenzofuranone)

快速询单

结构式：

4-羟基异苯并呋喃-1(3h)-酮MOL文件

CAS号：

13161-32-5

中文名称：

4-羟基异苯并呋喃-1(3h)-酮

英文名称：

4-hydroxy-1(3H)-Isobenzofuranone

分子式：

C₈H₆O₃

分子量：

150.131442546844

4-羟基异苯并呋喃-1(3h)-酮(13161-32-5)名称与标识符

名称

中文别名：

4-羟基异苯并呋喃-1(3h)-酮;

英文别名：

4-hydroxy-1(3H)-Isobenzofuranone;4-hydroxy-3H-2-benzofuran-1-one;4-Hydroxyisobenzofuran-1(3H)-one;4-hydroxy-2-benzofuran-1(3H)-one;4-hydroxy-3H-isobenzofuran-1-one;4-hydroxyphtalide;4-Hydroxy-phthalid;4-hydroxyphthalide;4-hydroxy-phthalide;AK-80804;ANW-68052;CTK8C2228;EN000416;KB-242370;SureCN78594;DTXSID60506053;4-Hydroxy-1(3H)-isobenzofuranone, 9CI;4-hydroxy-3H-2-benzouran-1-one;SY274862;1(3H)-Isobenzofuranone, 4-hydroxy-;CHEBI:178339;13161-32-5;CS-0324557;4-hydroxy-1,3-dihydro-2-benzofuran-1-one;WS-01368;SCHEMBL78594;AKOS005166872;MFCD15143974;ZSCIMKFWMUXNBS-UHFFFAOYSA-N;DB-332340;

标识符

MDL：

MFCD15143974

InChIKey：

ZSCIMKFWMUXNBS-UHFFFAOYSA-N

Inchi：

1S/C8H6O3/c9-7-3-1-2-5-6(7)4-11-8(5)10/h1-3,9H,4H2

SMILES：

O1C(C2C=CC=C(C=2C1)O)=O

4-羟基异苯并呋喃-1(3h)-酮(13161-32-5)物化性质

计算特性

精确分子量 : 150.031694049g/mol
氢键供体数量 : 1
氢键受体数量 : 3
可旋转化学键数量 : 0
同位素质量 : 150.031694049g/mol
重原子数量 : 11
复杂度 : 178
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : 1
拓扑分子极性表面积 : 46.5Å²

4-羟基异苯并呋喃-1(3h)-酮(13161-32-5)推荐厂家更多厂家(5)

公司名称	手机号/电话	联系人	QQ	询单
上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364	询单
北京百灵威科技有限公司	18210857532	翟先生	3650742139	询单
江苏艾康生物医药研发有限公司	18795912720 025-66061636	杨情情	3004779232	询单
上海麦克林生化科技股份有限公司	15221275939 021-50706066	沈经理	269348414	询单
上海源叶生物科技有限公司	15026964105 15026964105	汤思磊	2881489226	询单

4-羟基异苯并呋喃-1(3h)-酮(13161-32-5)相关文献

1. Nonpeptide small molecules from the insect Aspongopus chinensis and their neural stem cell proliferation stimulating properties
Lei Di,Yan-Ni Shi,Yong-Ming Yan,Li-Ping Jiang,Bo Hou,Xin-Long Wang,Zhi-Li Zuo,Yong-Bin Chen,Cui-Ping Yang,Yong-Xian Cheng RSC Adv. 2015 5 70985
2. Hybrid multidimensional data acquisition and data processing strategy for comprehensive characterization of known, unknown and isomeric compounds from the compound Dan Zhi Tablet by UPLC-TWIMS-QTOFMS
Taofang Cheng,Ji Ye,Huiliang Li,Hongyuan Dong,Ning Xie,Nan Mi,Zhen Zhang,Jingtao Zou,Huizi Jin,Weidong Zhang RSC Adv. 2019 9 8714
3. CXXIII.—4-Aminophthalide and some derivatives
Leopold Ferdinand Levy,Henry Stephen J. Chem. Soc. 1931 867
4. A new route to 4-hydroxytetralones and 1-naphthols
Nigel J. P. Broom,Peter G. Sammes J. Chem. Soc. Perkin Trans. 1 1981 465
5. Organic chemistry
J. Chem. Soc. Abstr. 1908 94 A593
6. 273. Infra-red spectroscopy and structural chemistry. Part V. Hydroxyphthalides
L. A. Duncanson,John Frederick Grove,J. Zealley J. Chem. Soc. 1953 1331
7. CLXXXVIII.—The calculation of the colour of “cyclic” coloured substances
James Moir J. Chem. Soc. Trans. 1921 119 1654
8. A new route to anthraquinones
David J. Dodsworth,María-Pía Calcagno,E. Ursula Ehrmann,Bhatt Devadas,Peter G. Sammes J. Chem. Soc. Perkin Trans. 1 1981 2120
9. Formula index
J. Chem. Soc. 1931 3445
10. Facile interconversion of the isomeric acid chlorides derived from half methyl esters of 3-methoxyphthalic acid
Dahmendra N. Gupta,Philip Hodge,Peter N. Hurley J. Chem. Soc. Perkin Trans. 1 1989 391