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4565-32-6 (2,3-二氢-1-苯并噻吩,2,3-dihydro-1-benzothiophene)

结构式：

2,3-二氢-1-苯并噻吩结构式图片|4565-32-6结构式图片

2,3-二氢-1-苯并噻吩MOL文件

CAS号：

4565-32-6

中文名称：

2,3-二氢-1-苯并噻吩

英文名称：

2,3-dihydro-1-benzothiophene

分子式：

C₈H₈S

分子量：

136.214120864868

相关分类：

溶剂及有机化学品 > 有机化合物 > Organosulfur compounds > Thioethers > Aryl thioethers

2,3-二氢-1-苯并噻吩(4565-32-6)名称与标识符

名称

英文别名：

2,3-dihydro-1-benzothiophene;2,3-Dihydrobenzothiophene;Benzo(b)thiophene, 2,3-dihydro-;benzo[b]thiophene, 2,3-dihydro-;2,3-Dihydrobenzo[b]thiophene;InChI=1/C8H8S/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H;AKOS025295343;2,3-dihydro-benzo[b]thiophene;DB-216649;2,3-Dihydro-1-benzothiophene #;SCHEMBL10884423;SCHEMBL8997;Dihydrobenzothiophene;MFCD18451841;Benzothiophane;1,3-Dihydrobenzothiophene;1-Thiaindan;AMY19129;DTXSID30963412;4565-32-6;2,3-dihydrobenzo(b)thiophen;

标识符

InChIKey：

YJUFGFXVASPYFQ-UHFFFAOYSA-N

Inchi：

1S/C8H8S/c1-2-4-8-7(3-1)5-6-9-8/h1-4H,5-6H2

SMILES：

S1C2C=CC=CC=2CC1

2,3-二氢-1-苯并噻吩(4565-32-6)物化性质

实验特性

PSA : 0

计算特性

精确分子量 : 136.03474
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 0
同位素质量 : 136.03467143g/mol
重原子数量 : 9
复杂度 : 101
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） : 2.5
拓扑分子极性表面积 : 25.3Å²

2,3-二氢-1-苯并噻吩(4565-32-6)推荐厂家更多厂家(2)

公司名称	手机号/电话	联系人	QQ	微信	询单
湖北鸿鑫瑞宇精细化工有限公司	17771822910 027-65385071	陈欣	2056564811		询单
JACS-郑州杰克斯化工产品有限公司	15981966935 0371-86259281	杰克斯JACS	893596907		询单

2,3-二氢-1-苯并噻吩(4565-32-6)相关文献

1. Toluene dioxygenase-catalyzed cis-dihydroxylation of benzo[b]thiophenes and benzo[b]furans: synthesis of benzo[b]thiophene 2,3-oxide
Derek R. Boyd,Narain D. Sharma,Ian N. Brannigan,Timothy A. Evans,Simon A. Haughey,Brian T. McMurray,John F. Malone,Peter B. A. McIntyre,Paul J. Stevenson,Christopher C. R. Allen Org. Biomol. Chem. 2012 10 7292
2. Stereoselective reductase-catalysed deoxygenation of sulfoxides in aerobic and anaerobic bacteria
Derek R. Boyd,Narain D. Sharma,Alistair W. T. King,Steven D. Shepherd,Christopher C. R. Allen,Robert A. Holt,Heather R. Luckarift,Howard Dalton Org. Biomol. Chem. 2004 2 554
3. Copper-catalyzed double C–S bond formation for the synthesis of 2-acyldihydrobenzo[b]thiophenes and 2-acylbenzo[b]thiophenes
Subramani Sangeetha,Govindasamy Sekar Chem. Commun. 2020 56 10906
4. Synthesis of novel 2,3-dihydro-8H-thieno[2,3-d]azepines and 1,2,3,4-tetrahydro-1H-3-benzazepines via photolyses of 6-azido-2,3-dihydrobenzo[b]thiophene and 6-azido-1,2,3,4-tetrahydronaphthalene
Christopher M. Daly,Brian Iddon,Hans Suschitzky,Ulrich Jordis,Fritz Sauter J. Chem. Soc. Perkin Trans. 1 1988 1933
5. Exploring relationships between chemical structure and molecular conductance: from α,ω-functionalised oligoynes to molecular circuits
Elena Gorenskaia,Jarred Potter,Marcus Korb,Colin Lambert,Paul J. Low Nanoscale 2023 15 10573
6. Enzyme-catalysed oxidation of 1,2-disulfides to yield chiral thiosulfinate, sulfoxide and cis-dihydrodiol metabolites
Derek R. Boyd,Narain D. Sharma,Steven D. Shepherd,Stig G. Allenmark,Christopher C. R. Allen RSC Adv. 2014 4 27607
7. Efficient synthesis of chiral 2,3-dihydro-benzo[b]thiophene 1,1-dioxides via Rh-catalyzed hydrogenation
Gongyi Liu,Heng Zhang,Yi Huang,Zhengyu Han,Gang Liu,Yuanhua Liu,Xiu-Qin Dong,Xumu Zhang Chem. Sci. 2019 10 2507
8. Bacterial dioxygenase- and monooxygenase-catalysed sulfoxidation of benzo[b]thiophenes
Derek R. Boyd,Narain D. Sharma,Brian McMurray,Simon A. Haughey,Christopher C. R. Allen,John T. G. Hamilton,W. Colin McRoberts,Rory A. More O'Ferrall,Jasmina Nikodinovic-Runic,Lydie A. Coulombel,Kevin E. O'Connor Org. Biomol. Chem. 2012 10 782
9. The syntheses, structures and spectroelectrochemical properties of 6-oxo-verdazyl derivatives bearing surface anchoring groups
Varshini J. Kumar,Jian-Zhong Wu,Martyna Judd,Elodie Rousset,Marcus Korb,Stephen A. Moggach,Nicholas Cox,Paul J. Low J. Mater. Chem. C 2022 10 1896
10. Copper-catalyzed synthesis of 2-acylbenzo[b]thiophenes from 3-(2-iodophenyl)-1-arylpropan-1-ones and potassium sulfide under aerobic conditions
Zhilei Zheng,Liang Chen,Cheng Qian,Xiaoming Zhu,Yuzhong Yang,Jianbing Liu,Yuan Yang,Yun Liang Org. Biomol. Chem. 2018 16 8020

目录

相关化合物

177365-43-4(7-tert-butyl-3,3-dimethyl-2H-1-benzothiophene) 14450-23-8(5-methyl-2,3-dihydro-1-benzothiophene) 6383-15-9(3-甲基-2,3-二氢-1-苯并噻吩) 813-67-2(2,2-Dimethylbutanoic acid methyl ester) 81426-14-4(8-乙酰氧基松脂醇) 80646-52-2(3’-叠氮基-5-[（E）-2-溴乙烯基]-2’，3’-二脱氧尿苷) 80651-74-7(（2beta，3beta，5beta，14xi，17alpha）-2,3,5,14,20-五羟基-22,25-环氧胆甾-7-烯-6-酮) 80690-65-9(3-氯-4-乙炔基苯胺)

问答

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