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(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE

Product Name
(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE
CAS No.
134856-58-9
Chemical Name
(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE
Synonyms
DK522;DKFELEX0125;TIMTEC-BB SBB009043;(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE;TRIMETHYLSILYL ETHYNYL-4-IODOBENZENE;1-iodo-4-(trimethylsilylethynyl)benzene;2-(4-iodophenyl)ethynyl-trimethylsilane;(4-Iodophenylethynyl)trimethylsilane 97%;1-Iodo-4-[2-(triMethylsilyl)ethynyl]-benzene;Benzene, 1-iodo-4-[2-(trimethylsilyl)ethynyl]-
CBNumber
CB7765252
Molecular Formula
C11H13ISi
Formula Weight
300.21
MOL File
134856-58-9.mol
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(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE Property

Melting point:
66-70 °C (lit.)
Boiling point:
265.4±32.0 °C(Predicted)
Density 
1.42±0.1 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
Powder
color 
White to yellow
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Safety

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2931900090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H319Causes serious eye irritation

H413May cause long lasting harmful effects to aquatic life

Precautionary statements

P273Avoid release to the environment.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
640751
Product name
(4-Iodophenylethynyl)trimethylsilane
Purity
97%
Packaging
1g
Price
$100.8
Updated
2025/07/31
Sigma-Aldrich
Product number
640751
Product name
(4-Iodophenylethynyl)trimethylsilane
Purity
97%
Packaging
5g
Price
$327.5
Updated
2025/07/31
Synthonix
Product number
K54599
Product name
((4-Iodophenyl)ethynyl)trimethylsilane
Purity
95+%
Packaging
5g
Price
$330
Updated
2021/12/16
Matrix Scientific
Product number
094182
Product name
((4-Iodophenyl)ethynyl)trimethylsilane
Purity
95+%
Packaging
5g
Price
$303
Updated
2021/12/16
Activate Scientific
Product number
AS88394
Product name
1-Iodo-4-[2-(trimethylsilyl)ethynyl]-benzene
Purity
95%
Packaging
5G
Price
$458
Updated
2021/12/16
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(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE Chemical Properties,Usage,Production

Synthesis

75867-39-9

134856-58-9

We optimized the synthesis steps. Deionized water (200 mL) and 4-[(trimethylsilyl)ethynyl]aniline (8.4 g, 44 mmol) were added to a 500 mL round-bottomed flask and stirred for 15 min at room temperature. Subsequently, concentrated hydrochloric acid (20.5 mL, 12 M) was slowly added to the reaction system and stirring was continued for 10 minutes. The reaction system was cooled to 0 °C and an aqueous solution of sodium nitrite (NaNO2, 3.96 g, 57 mmol) was added slowly and dropwise. The reaction system was kept stirred in an ice bath for 30 min. After that, the ice bath was removed and replaced by a room temperature water bath and stirring was continued for 30 min. After completion of the reaction, the aqueous phase was extracted with dichloromethane (3 x 100 mL). The organic phases were combined and transferred to another 1 L round-bottomed flask and placed in an ice bath and stirred for 10 min. An aqueous solution of potassium iodide (KI, 11.4 g, 69 mmol) was slowly added dropwise at 0 °C. The reaction mixture was allowed to warm up naturally to room temperature and stirring was continued for 6 hours. At the end of the reaction, the aqueous layer was extracted with ether. The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure to give the crude product. The crude product was purified by alumina column chromatography using petroleum ether as eluent to afford the target compound (4-iodophenylethynyl)trimethylsilane (11.3 g, 85% yield) as a white solid.IR (KBr, cm-1) ν: 2918, 2725, 2161, 1600, 1463, 1365, 1125, 1169, 951, 842, 750 , 723, 556, 471; 1H NMR (300 MHz, CDCl3, ppm) δ: 0.24 (s, 9H), 7.18 (d, J = 9.0 Hz, 2H), 7.63 (d, J = 9.0 Hz, 2H); 13C NMR (75 MHz, CDCl3, ppm) δ: -0.6, 93.9, 95.4, 103.5, 122.2, 132.9, 136.9.

References

[1] Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 2014, vol. 133, p. 229 - 240
[2] Journal of the American Chemical Society, 2001, vol. 123, # 34, p. 8177 - 8188
[3] Journal of Organic Chemistry, 2003, vol. 68, # 6, p. 2167 - 2174
[4] Tetrahedron, 1996, vol. 52, # 15, p. 5495 - 5504
[5] Tetrahedron, 2002, vol. 58, # 52, p. 10387 - 10405

(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE Preparation Products And Raw materials

Raw materials

Preparation Products

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(4-IODOPHENYLETHYNYL)TRIMETHYLSILANE Suppliers

Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Fax
021-64823266
Email
chenyj@titansci.com
Country
China
ProdList
14101
Advantage
59
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42934
Advantage
64
Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Amatek Scientific Co. Ltd.
Tel
0512-56316828 4008675858
Fax
+86-512-56316826
Email
sales@amateksci.com
Country
China
ProdList
9874
Advantage
55
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
39966
Advantage
60
Shanghai Gileader Advanced Material Technology Co.,Ltd
Tel
18516111942
Email
823898732@qq.com
Country
China
ProdList
1328
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56
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51395
Advantage
80
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60

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