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ChemicalBook >> CAS DataBase List >>2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE

CAS No.
88284-48-4
Chemical Name:
2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE
Synonyms
2-(Trimethylsilyl)phenyl Triflate;DK943;DKSI110;DKFELEX0252;(TriMethylsilyl)phenyl Triflate;TriMethylsilyl)phenyl trifluoroMethanesulfona;2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFOTE;2-(trimethylsilyl)phenyl trifluoromethane-sulfona;2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE;2-(TriMethylsilyl)phenyl trifluoroMethanesulfonate 97%
CBNumber:
CB5399688
Molecular Formula:
C10H13F3O3SSi
Molecular Weight:
298.35
MDL Number:
MFCD00799598
MOL File:
88284-48-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 03:29:55
Product description Number Pack Size Price
2-(Trimethylsilyl)phenyl trifluoromethanesulfonate 97% 470430 1g $71.5
2-(Trimethylsilyl)phenyl trifluoromethanesulfonate 97% 470430 5g $223
2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate >95.0%(GC) T2089 1g $53
2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate >95.0%(GC) T2089 5g $160
2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate Asreported 291582 2g $337
More product size

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE Properties

Boiling point 70 °C/2 mmHg (lit.)
Density 1.229 g/mL at 25 °C (lit.)
refractive index n20/D 1.456(lit.)
Flash point 205 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form clear liquid
color Colorless to Light yellow
Specific Gravity 1.229
Hydrolytic Sensitivity 7: reacts slowly with moisture/water
InChI InChI=1S/C10H13F3O3SSi/c1-18(2,3)9-7-5-4-6-8(9)16-17(14,15)10(11,12)13/h4-7H,1-3H3
InChIKey XBHPFCIWRHJDCP-UHFFFAOYSA-N
SMILES C(F)(F)(F)S(OC1=CC=CC=C1[Si](C)(C)C)(=O)=O
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P280-P305+P351+P338-P310
PPE Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Codes  C
Risk Statements  34
Safety Statements  26-27-36/37/39-45
RIDADR  UN 3265 8/PG 2
WGK Germany  3
HazardClass  8
PackingGroup 
HS Code  29319090
Storage Class 8A - Combustible corrosive hazardous materials
Limited Quantities 1.0 L (0.3 gallons) (liquid) or 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
0 0

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE price More Price(87)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 470430 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate 97% 88284-48-4 1g $71.5 2024-03-01 Buy
Sigma-Aldrich 470430 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate 97% 88284-48-4 5g $223 2024-03-01 Buy
TCI Chemical T2089 2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate >95.0%(GC) 88284-48-4 1g $53 2026-04-30 Buy
TCI Chemical T2089 2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate >95.0%(GC) 88284-48-4 5g $160 2026-04-30 Buy
Usbiological 291582 2-(Trimethylsilyl)phenyl Trifluoromethanesulfonate Asreported 88284-48-4 2g $337 2026-06-03 Buy
Product number Packaging Price Buy
470430 1g $71.5 Buy
470430 5g $223 Buy
T2089 1g $53 Buy
T2089 5g $160 Buy
291582 2g $337 Buy

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE Chemical Properties,Uses,Production

Chemical Properties

The chemical properties of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate are mainly derived from the trifluoromethanesulfonyl and trimethylsilyl groups in its structure. As a strongly acidic leaving group, trifluoromethanesulfonyl is easily dissociated in reactions to form stable fluoride ions and trifluoromethanesulfonyl cations. This property makes it exhibit excellent catalytic performance in catalyzing esterification, etherification, condensation and other reactions. Meanwhile, the trimethylsilyl group, as a stable substituent, not only enhances the stability of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate, but also provides the possibility of its wide application in organic synthesis.

Physical properties

bp 70 °C/2 mmHg; d 1.229 g mL1

Uses

2-(Trimethylsilyl)phenyl trifluoromethanesulfonate may be used to generate benzyne under mild conditions of simple fluoride treatment at room temperature.

Uses

2-(Trimethylsilyl)phenyl Triflate is a useful reagent applied in reactions of Polycyclic Arenes, Heteroatom Arylation,Heteroarenes and Benzannulated Heterocycles, Carbon Arylations, etc.	2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE

General Description

2-(Trimethylsilyl)phenyl trifluoromethanesulfonate is an important ortho-benzyne precursor in aryne chemistry.

Synthesis

Trifluoromethanesulfonic anhydride

358-23-6

o-(Trimethylsilyl)phenol

15288-53-6

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE

88284-48-4

(1) In a 10 L glass reactor, after argon displacement, 6 L of dichloromethane and 1 kg of 2-(trimethylsilyl)phenol (compound III) were added and mixed thoroughly. (2) The reaction system was cooled to -10 to -15 °C using a dry ice-ethanol bath, and 550 g of pyridine was added slowly and dropwise, and the reaction was exothermic and accompanied by the generation of white fumes. (3) Maintain the internal temperature below -10°C and slowly add 1.8 kg of trifluoromethanesulfonic anhydride dropwise. (4) After the dropwise addition, the reaction was carried out at -5 to 0°C for 5 to 6 hours. (5) After confirming the complete consumption of Compound III by GC monitoring, the reaction system was cooled to below 0°C, and the reaction was quenched by slow dropwise addition of 1.5L of 1N hydrochloric acid solution, taking care to control the exotherm. (6) After quenching and stirring, static layering, the organic phase was washed with 2L of saturated sodium bicarbonate solution and 2L of saturated sodium chloride solution, 100g of anhydrous magnesium sulfate drying, filtration and concentration under reduced pressure, to obtain 1.5kg of brown transparent liquid 2-(trimethylmethylsilyl)phenyl trifluoromethanesulfonate (Compound IV). (7) 1.5kg of crude compound IV was transferred to a 2L distillation flask and distilled under reduced pressure. Under 1.0 kPa vacuum, the bath temperature was 91~105°C, boiling point 49~76°C, the pre-fraction F1 (65 g) was collected; the bath temperature was 108~110°C, boiling point 76~79°C, the main fraction F2 (1.32 kg, GC purity 98.7%) was collected; the distillation was stopped and the residue F3 (85 g).

References

[1] Synthesis, 2010, # 6, p. 911 - 913
[2] Organic and Biomolecular Chemistry, 2016, vol. 14, # 25, p. 6079 - 6087
[3] Patent: CN107325120, 2017, A. Location in patent: Paragraph 0039; 0040; 0041; 0042; 0043; 0044; 0045-0052

358-23-6
15288-53-6
88284-48-4
Synthesis of 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE from Trifluoromethanesulfonic anhydride and o-(Trimethylsilyl)phenol
Global( 197)Suppliers
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View Lastest Price from 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-trimethylsilylphenyl triflate pictures 2026-04-17 2-trimethylsilylphenyl triflate
88284-48-4
$2.20-8.80 1kg 99%min 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
(TriMethylsilyl)phenyl Triflate pictures 2026-02-02 (TriMethylsilyl)phenyl Triflate
88284-48-4
$1.00 1g 99% 50ton Shaanxi Dideu Medichem Co. Ltd
2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE pictures 2025-04-04 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE
88284-48-4
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.

2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE Spectrum

Trifluoromethanesulfonic Acid 2-(Trimethylsilyl)phenyl Ester 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE 2-(trimethylsilyl)phenyl trifluoromethane-sulfona 2-(Trimethylsilyl)phenyl Triflate Trifluoromethanesulfonic Acid 2-(Trimethylsilyl)phenyl Ester (TriMethylsilyl)phenyl Triflate TriMethylsilyl)phenyl trifluoroMethanesulfona 2-(TriMethylsilyl)phenyl trifluoroMethanesulfonate 97% 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFOTE Methanesulfonic acid, 1,1,1-trifluoro-, 2-(trimethylsilyl)phenyl ester 88284-48-4 2-(TRIMETHYLSILYL)PHENYL TRIFLUOROMETHANESULFONATE DK943 DKFELEX0252 DKSI110 2-(Trimethylsilyl)phenyl Triflate 88284-48-4 CF3SO3C6H4SiCH33 C10H13F3O3SSi Building Blocks Organic Building Blocks Sulfur Compounds Organic Triflates Si (Classes of Silicon Compounds) Si-(C)4 Compounds Silicon Compounds (for Synthesis) Synthetic Organic Chemistry Organic Triflates Organic Building Blocks Sulfur Compounds
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