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DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)

CAS No.
85272-31-7
Chemical Name:
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)
Synonyms
DI-TERT-BUTYLBIS(TRIFLUOROMETHANESULFONYLOXY)SILANE;Di-tert-butylsilanediyl bis(trifluoroMethanesulfonate);DTBS DITRIFLATE;Di-T-Butylsilylbis;DI-T-BUTYLSILYL DITRIFLATE;DI-TERT-BUTYLSILYL DITRIFLATE;BIS(TRIFLUOROMETHANESULFONATE);85272-31-7 DI-TERT-BUTYLSILYL DITRIFLATE;Di-tert-butylsilylbis(trifluoromethanesul;Di-t-butylsilybis(trifluoromethanesulfonate
CBNumber:
CB3337556
Molecular Formula:
C10H18F6O6S2Si
Molecular Weight:
440.45
MDL Number:
MFCD00010581
MOL File:
85272-31-7.mol
MSDS File:
SDS
Last updated:2024-02-13 10:22:34

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) Properties

Boiling point 73-75 °C/0.35 mmHg (lit.)
Density 1.352 g/mL at 25 °C (lit.)
refractive index n20/D 1.398(lit.)
Flash point 195 °F
storage temp. Inert atmosphere,Room Temperature
solubility sol most common organic solvents.
form Oil
color Clear Pale Yellow
Specific Gravity 1.358
Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents
BRN 3569211
Stability Moisture Sensitive
InChIKey HUHKPYLEVGCJTG-UHFFFAOYSA-N
CAS DataBase Reference 85272-31-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P280-P301+P330+P331-P303+P361+P353-P304+P340+P310-P305+P351+P338-P363
Hazard Codes  C
Risk Statements  34
Safety Statements  26-36/37/39-45
RIDADR  UN 3265 8/PG 2
WGK Germany  3
10-21
Hazard Note  Corrosive
TSCA  No
HazardClass  8
PackingGroup  III
HS Code  29319090
NFPA 704
2
3 0

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) price More Price(24)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 262021 Di-tert-butylsilyl bis(trifluoromethanesulfonate) 97% 85272-31-7 5g $134 2024-03-01 Buy
Sigma-Aldrich 262021 Di-tert-butylsilyl bis(trifluoromethanesulfonate) 97% 85272-31-7 25g $445 2024-03-01 Buy
TCI Chemical D3135 Di-tert-butylsilyl Bis(trifluoromethanesulfonate) >97.0%(T) 85272-31-7 1g $47 2024-03-01 Buy
TCI Chemical D3135 Di-tert-butylsilyl Bis(trifluoromethanesulfonate) >97.0%(T) 85272-31-7 5g $141 2024-03-01 Buy
Sigma-Aldrich 262021 Di-tert-butylsilyl bis(trifluoromethanesulfonate) 97% 85272-31-7 250g $1616 2024-03-01 Buy
Product number Packaging Price Buy
262021 5g $134 Buy
262021 25g $445 Buy
D3135 1g $47 Buy
D3135 5g $141 Buy
262021 250g $1616 Buy

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) Chemical Properties,Uses,Production

Chemical Properties

Colorless to yellow liquid

Physical properties

bp 73–75°C/0.35 mmHg; d 1.208 g cm?3.

Uses

Protecting group reagent for 1,3-diols used recently in a synthesis of N-homoceramides. Also used for selective α-galactosylation in the synthesis of α-galactosyl ceramides.

Uses

Di-t-butylsilyl bis(trifluoromethanesulfonate) is a reagent for the selective protection of polyhydroxy compounds. This reagent reacts with 1,2-, 1,3-, and 1,4-diols under mild conditions to give the corresponding dialkylsilylene derivatives in high yield (0–50°C, 79–96%). Deprotection is conveniently achieved by using aqueous hydrofluoric acid in acetonitrile (eq 1).
Unlike di-t-butyldichlorosilane, this reagent reacts with hindered alcohols. Even pinacol reacts to give the silylene derivative (100°C, 24 h, 70%). Di-t-butylsilylene derivatives of 1,2-diols are more reactive than those of 1,3- and 1,4-diols and undergo rapid hydrolysis (5 min) in THF/H2O at pH 10, while the 1,3- and 1,4- derivatives are unaffected at pH 4–10 (22°C) for several hours. This protecting group is stable under the conditions of PDC oxidation of alcohols (CH2Cl2, 25?C, 27 h) and tosylation of alcohols (pyridine, 25°C, 27 h).
The reagent has seen limited use for the protection of alcohols but has been used to protect nucleosides (eq 2).The procedure consists of sequential addition of the ditriflate and triethylamine to the nucleoside in DMF. The choice of solvent is critical.Di-t-butylsilyl bis(trifluoromethanesulfonate)

Preparation

by the treatment of di-t-butylchlorosilane with trifluoromethanesulfonic acid, followed by distillation (71% yield).

1493-13-6
56310-18-0
85272-31-7
Synthesis of DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) from Trifluoromethanesulfonic acid and DI-TERT-BUTYLCHLOROSILANE

DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) Preparation Products And Raw materials

Global( 190)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Shanghai Daken Advanced Materials Co.,Ltd
+86-371-66670886 info@dakenam.com China 15371 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21695 55
Nanjing ChemLin Chemical Industry Co., Ltd.
025-83697070 product@chemlin.com.cn CHINA 3012 60
Fluoropharm Co., Ltd.
+86-0571-85586753; +8613336034509 sales@fluoropharm.com China 1290 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Jinan Carbotang Biotech Co.,Ltd.
+8615866703830 figo.gao@foxmail.com China 6992 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5909 58
Changzhou Carman Chemical Co., Ltd.
15061933924 CHINA 514 58

View Lastest Price from DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Bis(tert-butyl)silyl bis(trifluoromethanesulphonate) pictures 2024-02-13 Bis(tert-butyl)silyl bis(trifluoromethanesulphonate)
85272-31-7
US $700.00 / g 1g 98 500 Kg R&D Scientific Inc.
Bis(trifluoromethanesulfonic acid)di-tert-butylsilanediyl ester pictures 2022-09-24 Bis(trifluoromethanesulfonic acid)di-tert-butylsilanediyl ester
85272-31-7
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) pictures 2019-07-06 DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE)
85272-31-7
US $1.00 / KG 1G 98% 100KG Career Henan Chemical Co
TRIFLUOROMETHANESULFONIC ACID DI-TERT-BUTYLSILYLENE ESTER DI-T-BUTYLSILYLBIS(TRIFLUOROMETHANESULFONATE) DI(T-BUTYL)SILYL BIS(TRIFLUOROMETHANESULPHONATE) DI-T-BUTYLSILYL DITRIFLATE DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULFONATE) DI-TERT-BUTYLSILYL BIS(TRIFLUOROMETHANESULPHONATE) DI-TERT-BUTYLSILYL DITRIFLATE DTBS DITRIFLATE Di-t-butylsilybis(trifluoromethanesulfonate Bis(trifluoromethanesulfonic acid)[di(1,1-dimethylethyl)silanediyl] ester Bis(trifluoromethanesulfonic acid)di-tert-butylsilanediyl ester Di-tert-butylbis(trifluoromethylsulfonyloxy)silane Methanesulfonic acid, trifluoro-, bis(1,1-dimethylethyl)silylene ester BIS(TRIFLUOROMETHANESULFONATE) Di-tert-butylsilyl ditriflate, DTBS ditriflate, Trifluoromethanesulfonic acid di-tert-butylsilylene ester Di-tert-butylsilybis(trifluoromethanesulfonate Di-tert-butylbis(trifluoromethanesulfonyloxy)silane Di-tert-butylsilyl Ditriflate Methanesulfonic acid, 1,1,1-trifluoro-, bis(1,1-diMethylethyl)[[(trifluoroMethyl)sulfonyl]oxy]silyl ester Bis(tert-butyl)silyl bis(trifluoromethanesulphonate) Bis(tert-butyl)silyl ditriflate, DTBS ditriflate, DTBSDT Di-T-Butylsilylbis Di-tert-butylsilylBis(trifluoromethanesulfonate)> Di-tert-butylsilyl bis(trifluoromethanesulfonate), 97%, for synthesis 85272-31-7 DI-TERT-BUTYLSILYL DITRIFLATE DI-TERT-BUTYLBIS(TRIFLUOROMETHANESULFONYLOXY)SILANE Di-tert-butylsilanediyl bis(trifluoroMethanesulfonate) Bis(1,1-dimethylethyl)[[(trifluoromethyl)sulfonyl]oxy]silyl 1,1,1-trifluoromethanesulfonate Di-tert-butylsilylbis(trifluoromethanesul Bis(tert-butyl)[[(trifluoromethyl)sulfonyl]oxy]silyl triflate 85272-31-7 C10H18F6O6S2Si CF3SO32SiCCH332 C10H18O6F6S2Si Organic Triflates Protecting and Derivatizing Reagents Protection and Derivatization Organic Building Blocks Building Blocks Silicon Compounds (for Synthesis) Si (Classes of Silicon Compounds) Si-O Compounds Silyl Esters Silicon-Based Sulfur Compounds Synthetic Reagents Si (Classes of Silicon Compounds) Silicon Compounds (for Synthesis) Silyl Esters Si-O Compounds Synthetic Organic Chemistry