二苯基氯硅烷 | 1631-83-0
中文名称:
二苯基氯硅烷
英文名称:
Chlorodiphenylsilane
CAS No.:
1631-83-0
分子式:
C1 2 H1 0 ClSi
分子量:
217.7463
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:二苯基氯硅烷结构式
名称和标识符
MDL
MFCD00045144
InChIKey
YCITZMJNBYYMJO-UHFFFAOYSA-N
Inchi
1S/C12H10ClSi/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
SMILES
Cl[Si](C1C([H])=C([H])C([H])=C([H])C=1[H])C1C([H])=C([H])C([H])=C([H])C=1[H] |^1:1|
BRN
2937164
别名信息
- 中文别名 -
二苯基氯硅烷
氯化二苯基硅烷
二苯基一氯一氢硅烷
氯二苯基硅烷
氯二苯基硅烷, TECH
二苯基氯硅烷, 90+%
二苯基一氯一氢硅烷 25G
- 英文别名 -
Diphenylchlorosilane
Chlorodiphenylsilane
DIPHENYLCHLOROSILANE, tech-95
chloro(diphenyl)silicon
Diphenylsilyl chloride
chlorodiphenyl-silan
Silane, chlorodiphenyl-
Benzene, 1,1'-(chlorosilylene)bis-
Chlorodiphenylsilane, 90+%
CHLORODIPHENYLSILANE, TECH., 90%
Chlorodiphenylsilane technical grade, 90%
Chloro(diphenyl)silane
C12H11ClSi
8289AA
FCH1321874
S07725
DIPHENYLCHLOROSILANE
CHLORODIPHENYLSILANE
FT-0604877
SCHEMBL297217
MFCD00045144
DTXSID90883703
A851797
J-010016
1631-83-0
Chlorodiphenylsilane.
?DIPHENYLCHLOROSILANE
AKOS016010259
EINECS 216-634-8
DIPHENYLCHLOROSILANE, tech
物化性质
实验特性
LogP
1.76340
PSA
0.00000
折射率
n20/D 1.578(lit.)
水溶性
Reacts with water.
沸点
143 °C/10 mmHg(lit.)
蒸气压
0.0±0.5 mmHg at 25°C
闪点
华氏:221 °F 摄氏:105 °C
溶解度
Insuluble (6.1E-4 g/L) (25 ºC),
颜色与性状
无色或灰黄色液体。
溶解性
反应。
敏感性
Moisture Sensitive
密度
1.118 g/mL at 25 °C(lit.)
计算特性
精确分子量
218.03200
氢键供体数量
0
氢键受体数量
0
可旋转化学键数量
2
同位素质量
217.02403
重原子数量
14
复杂度
142
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)
无
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
0
海关数据
海关编码
2931900090
海关数据
中国海关编码:
2931900090
概述:
2931900090. 其他有机-无机化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:AB(入境货物通关单,出境货物通关单). 最惠国关税:6.5%. 普通关税:30.0%
Summary:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%
相关文献
1.
Stereocontrol in organic synthesis using silicon-containing compounds. A formal synthesis of prostaglandins controlling the stereochemistry at C-15 using a silyl-to-hydroxy conversion following a stereochemically convergent synthesis of an allylsilane
Ian Fleming,Stephen B. D. Winter J. Chem. Soc. Perkin Trans. 1 1998 2687
2.
Synthesis and characterization of poly(tetraphenylimidazole)s and their application in the detection of fluoride ions
Basava Punna Rao Aradhyula,Ramu V. Ranga Naidu Chinta,Kunchala Dhanunjayarao,Krishnan Venkatasubbaiah RSC Adv. 2020 10 13149
3.
Complete tetraglycosylation of a calix[4]arene by a chemo-enzymatic approach
Silvia Bernardi,Dong Yi,Ning He,Alessandro Casnati,Wolf-Dieter Fessner,Francesco Sansone Org. Biomol. Chem. 2017 15 10064
4.
Nitrogen–boron coordination versus OH?N hydrogen bonding in pyridoxaboroles – aza analogues of benzoxaboroles
I. Steciuk,K. Durka,K. Gontarczyk,M. D?browski,S. Luliński,K. Wo?niak Dalton Trans. 2015 44 16534
5.
Synthesis, structure, and ethene polymerisation catalysis of 1- or 2-silyl substituted bis[indenyl]zirconium(iv) dichlorides
Andreas C. M?ller,Richard H. Heyn,Richard Blom,Ole Swang,Carl Henrik G?rbitz,Jürgen Kopf Dalton Trans. 2004 1578
6.
Polymer compositions on kinetic resolution of secondary alcohols using polymer-supported silyl chlorides
Tian Zhang,Shelby D. Dickerson,Tianyu Zhu,Chuanbing Tang,Sheryl L. Wiskur Polym. Chem. 2020 11 5011
7.
A spherosilicate oligomer with eight stable silanol groups as a building block of hybrid materials
Kazufumi Kawahara,Hiroki Tachibana,Yoshiaki Hagiwara,Kazuyuki Kuroda New J. Chem. 2012 36 1210
8.
Synthesis and characterisation of novel o-xylene-based P,E ligands
Kathryn M. Allan,John L. Spencer Org. Biomol. Chem. 2014 12 956
9.
Phosphorescent Ir(iii) complexes with both cyclometalate chromophores and phosphine-silanolate ancillary: concurrent conversion of organosilane to silanolate
Fushi Zhang,Liduo Wang,Shih-Han Chang,Kuan-Lin Huang,Yun Chi,Wen-Yi Hung,Chih-Ming Chen,Gene-Hsiang Lee,Pi-Tai Chou Dalton Trans. 2013 42 7111
10.
A direct route to a novel tetraphenyldisilabicyclo[2.2.2.]octa-2,5-diene: a tetraphenyldisilene precursor
Clifford L. Smith,Janet Pounds J. Chem. Soc. Chem. Commun. 1975 910
参考资料
Reaxys RN
Beilstein
2937164
960化工网为您提供二苯基氯硅烷专业化合物百科信息,包括中文名,英文名,分子式,分子量,以及该化合物的CasNo.:1631-83-0,和相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等