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25561-30-2

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25561-30-2 Usage

Uses

Different sources of media describe the Uses of 25561-30-2 differently. You can refer to the following data:
1. Used for synthesis of pharmaceutical intermediates.
2. Used as a reactant in the preparation of pyrimidinone ribosides and analogs that show anti-tumor properties.
3. N,O-bis(trimethylsilyl)-trifluoroacetamide (BSTFA) is similar to BSA in specificity of modification and there are several studies which have used both reagents.One study found BSTFA superior to BSA in product stability and yield of derivative. Another study compared several trimethylsilyl donors for end-capping of silica and observed that BSTFA was more reactive than BSA but less reactive than TMCim. Both BSA and BSTFA were used to prepare trimethylsilyl derivatives of pyrimidines and purines.Current work has used BSTFA for metabolomics analysis of urine,for the measurement of khatamines (psychoactive amines of khat (Catha edulis Forsk), and for the measurement of acrylamide in cocoa.
4. N,O-Bis(trimethylsilyl)trifluoroacetamide is used for analytical purposes or as a chemical reagent for synthesis of more complex molecules. It is silylation reagent useful in GC and GC-MS for the derivatization of a wide range of functional groups under mild conditions. It is also used as DAT inhibitor and a SLC6A2 inhibitor. It is routinely used to derivatize carboxylic acids, phenols, steroids, amines, alcohols, and alkaloids and amides.

Chemical Properties

Clear to yellowish clear liquid

Definition

ChEBI: A silyl ether that is the N,O-bis(trimethylsilyl) derivative of trifluoroacetamide. N,O-bis(trimethylsilyl)trifluoroacetamide is a derivatisation agent used in gas chromatography/m ss spectrometry applications.

General Description

N,O-Bis(trimethylsilyl)trifluoroacetamide with trimethylchlorosilane has found application to be used in gas chromatography (GC) and mass-spectrometry (MS). It can also be used in HPLC- electrochemical detection assay of 8-oxo-deoxyguanosine and?8-oxo-guanine.

Check Digit Verification of cas no

The CAS Registry Mumber 25561-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,5,6 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25561-30:
(7*2)+(6*5)+(5*5)+(4*6)+(3*1)+(2*3)+(1*0)=102
102 % 10 = 2
So 25561-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H18F3NOSi2/c1-14(2,3)8(9,15(4,5)6)7(13)12(10)11/h1-6H3

25561-30-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B0830)  N,O-Bis(trimethylsilyl)trifluoroacetamide  >95.0%(GC)

  • 25561-30-2

  • 5mL

  • 295.00CNY

  • Detail
  • TCI America

  • (B0830)  N,O-Bis(trimethylsilyl)trifluoroacetamide  >95.0%(GC)

  • 25561-30-2

  • 25mL

  • 790.00CNY

  • Detail
  • TCI America

  • (B0830)  N,O-Bis(trimethylsilyl)trifluoroacetamide  >95.0%(GC)

  • 25561-30-2

  • 100mL

  • 2,750.00CNY

  • Detail
  • TCI America

  • (A5603)  BSTFA [=N,O-Bis(trimethylsilyl)trifluoroacetamide] [for Gas Chromatography]  >95.0%(GC)

  • 25561-30-2

  • 5mL

  • 590.00CNY

  • Detail
  • Alfa Aesar

  • (42429)  N,O-Bis(trimethylsilyl)trifluoroacetamide, 99+%, packaged under Argon in resealable ChemSeal? bottles   

  • 25561-30-2

  • 5g

  • 288.0CNY

  • Detail
  • Alfa Aesar

  • (42429)  N,O-Bis(trimethylsilyl)trifluoroacetamide, 99+%, packaged under Argon in resealable ChemSeal? bottles   

  • 25561-30-2

  • 25g

  • 1209.0CNY

  • Detail
  • Alfa Aesar

  • (42429)  N,O-Bis(trimethylsilyl)trifluoroacetamide, 99+%, packaged under Argon in resealable ChemSeal? bottles   

  • 25561-30-2

  • 100g

  • 2320.0CNY

  • Detail
  • Alfa Aesar

  • (40174)  N,O-Bis(trimethylsilyl)trifluoroacetamide, with 10% TMCS   

  • 25561-30-2

  • 5g

  • 295.0CNY

  • Detail
  • Alfa Aesar

  • (40174)  N,O-Bis(trimethylsilyl)trifluoroacetamide, with 10% TMCS   

  • 25561-30-2

  • 25g

  • 1159.0CNY

  • Detail
  • Alfa Aesar

  • (40174)  N,O-Bis(trimethylsilyl)trifluoroacetamide, with 10% TMCS   

  • 25561-30-2

  • 100g

  • 3541.0CNY

  • Detail
  • Alfa Aesar

  • (43939)  N,O-Bis(trimethylsilyl)trifluoroacetamide, with 1% TMCS   

  • 25561-30-2

  • 5g

  • 402.0CNY

  • Detail
  • Alfa Aesar

  • (43939)  N,O-Bis(trimethylsilyl)trifluoroacetamide, with 1% TMCS   

  • 25561-30-2

  • *5x1g

  • 583.0CNY

  • Detail

25561-30-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N,O-bis(trimethylsilyl)trifluoroacetamide

1.2 Other means of identification

Product number -
Other names N,O-bis-TMS-trifluoroacetamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25561-30-2 SDS

25561-30-2Synthetic route

trifluoracetyl chloride
354-32-5

trifluoracetyl chloride

sodium hexamethyldisilazane
1070-89-9

sodium hexamethyldisilazane

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

2,2,2-trifluoroacetamide
354-38-1

2,2,2-trifluoroacetamide

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

Conditions
ConditionsYield
With triethylamine
With triethylamine
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

(+/-)-7β,8α-bis(trimethylsilyloxy)-9α,10α-epoxy-7,8,9,10-tetrahydrobenzopyrene
64660-75-9, 134175-49-8

(+/-)-7β,8α-bis(trimethylsilyloxy)-9α,10α-epoxy-7,8,9,10-tetrahydrobenzopyrene

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 3h; Ambient temperature;100%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

2-(o-chlorophenyl)-2-<(methoxycarbonyl)amino>-6-hydroxycyclohexanone
103904-70-7

2-(o-chlorophenyl)-2-<(methoxycarbonyl)amino>-6-hydroxycyclohexanone

[(1S,3S)-1-(2-Chloro-phenyl)-2-oxo-3-trimethylsilanyloxy-cyclohexyl]-carbamic acid methyl ester
103904-71-8

[(1S,3S)-1-(2-Chloro-phenyl)-2-oxo-3-trimethylsilanyloxy-cyclohexyl]-carbamic acid methyl ester

Conditions
ConditionsYield
With pyridine In dichloromethane for 1h; Heating;100%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

phenyl (2R*,5Z,9S*,10S*,16R*)-9-hydroxy-9-methyl-10,2,10-(epoxymetheno)-1-benzazacyclododeca-5-ene-3,7-diyne-1-carboxylate

phenyl (2R*,5Z,9S*,10S*,16R*)-9-hydroxy-9-methyl-10,2,10-(epoxymetheno)-1-benzazacyclododeca-5-ene-3,7-diyne-1-carboxylate

phenyl (2R*,5Z,9S*,10S*,16R*)-9-methyl-9-trimethylsilyloxy-10,2,10-(epoxymetheno)-1-benz[b]azacyclododeca-5-ene-3,7-diyne-1-carboxylate

phenyl (2R*,5Z,9S*,10S*,16R*)-9-methyl-9-trimethylsilyloxy-10,2,10-(epoxymetheno)-1-benz[b]azacyclododeca-5-ene-3,7-diyne-1-carboxylate

Conditions
ConditionsYield
With pyridine at 25℃; for 44h;100%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
With potassium acetate; bis(η3-allyl-μ-chloropalladium(II)) In tetrahydrofuran99%
With potassium acetate; bis(η3-allyl-μ-chloropalladium(II)) In dichloromethane98.9%
With lithium carbonate; bis(η3-allyl-μ-chloropalladium(II)) In toluene94%
lithium carbonate. tert-Butyl methyl ether

lithium carbonate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))99%
bis(η3-allyl-μ-chloropalladium(II))91%
bis(η3-allyl-μ-chloropalladium(II))88%
bis(η3-allyl-μ-chloropalladium(II))86%
bis(η3-allyl-μ-chloropalladium(II))71%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

(E)-2-(o-Chlorophenyl)-6-hydroxy-2-<(methoxycarbonyl)methylamino>cyclohexanone
91003-20-2

(E)-2-(o-Chlorophenyl)-6-hydroxy-2-<(methoxycarbonyl)methylamino>cyclohexanone

[(1S,3R)-1-(2-Chloro-phenyl)-2-oxo-3-trimethylsilanyloxy-cyclohexyl]-methyl-carbamic acid methyl ester
91003-26-8

[(1S,3R)-1-(2-Chloro-phenyl)-2-oxo-3-trimethylsilanyloxy-cyclohexyl]-methyl-carbamic acid methyl ester

Conditions
ConditionsYield
With pyridine In dichloromethane for 2h; Heating;96.5%
N-Boc-methylthiolincosamide
663613-82-9

N-Boc-methylthiolincosamide

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

C26H59NO7SSi4
844504-73-0

C26H59NO7SSi4

Conditions
ConditionsYield
With triethylamine In DMF (N,N-dimethyl-formamide) at 0 - 20℃;95%
lithium carbonate. tert-Butyl methyl ether

lithium carbonate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

dimethyl 2-(cyclohex-2-en-1-yl)malonate
34939-28-1

dimethyl 2-(cyclohex-2-en-1-yl)malonate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))93%
bis(η3-allyl-μ-chloropalladium(II))56%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

10-TMS-10-deacetylbaccatin III

10-TMS-10-deacetylbaccatin III

Conditions
ConditionsYield
In tetrahydrofuran at 0℃; for 5h;91%
In tetrahydrofuran at 0℃; for 5h;91%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

10-trimethylsilyl-10-desacetylbaccatin III monohydrate

10-trimethylsilyl-10-desacetylbaccatin III monohydrate

Conditions
ConditionsYield
In tetrahydrofuran at 0℃; for 5h; Under N2;91%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

{(2R,3S)-3-((R)-1-Hydroxy-ethyl)-2-[2-(4-nitro-benzyloxycarbonylamino)-ethylsulfanylcarbonylmethyl]-4-oxo-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester
92133-39-6

{(2R,3S)-3-((R)-1-Hydroxy-ethyl)-2-[2-(4-nitro-benzyloxycarbonylamino)-ethylsulfanylcarbonylmethyl]-4-oxo-azetidin-1-yl}-oxo-acetic acid 4-nitro-benzyl ester

[(2R,3S)-2-[2-(4-Nitro-benzyloxycarbonylamino)-ethylsulfanylcarbonylmethyl]-4-oxo-3-((R)-1-trimethylsilanyloxy-ethyl)-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester
90629-05-3

[(2R,3S)-2-[2-(4-Nitro-benzyloxycarbonylamino)-ethylsulfanylcarbonylmethyl]-4-oxo-3-((R)-1-trimethylsilanyloxy-ethyl)-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester

Conditions
ConditionsYield
dmap In tetrahydrofuran90%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

[(2R,3S)-3-((R)-1-Hydroxy-ethyl)-2-((S)-1-{1-[(E)-4-nitro-benzyloxycarbonylimino]-ethyl}-pyrrolidin-3-ylsulfanylcarbonylmethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester
92133-41-0

[(2R,3S)-3-((R)-1-Hydroxy-ethyl)-2-((S)-1-{1-[(E)-4-nitro-benzyloxycarbonylimino]-ethyl}-pyrrolidin-3-ylsulfanylcarbonylmethyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester

[(2R,3S)-2-((S)-1-{1-[(E)-4-Nitro-benzyloxycarbonylimino]-ethyl}-pyrrolidin-3-ylsulfanylcarbonylmethyl)-4-oxo-3-((R)-1-trimethylsilanyloxy-ethyl)-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester
98167-71-6

[(2R,3S)-2-((S)-1-{1-[(E)-4-Nitro-benzyloxycarbonylimino]-ethyl}-pyrrolidin-3-ylsulfanylcarbonylmethyl)-4-oxo-3-((R)-1-trimethylsilanyloxy-ethyl)-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester

Conditions
ConditionsYield
dmap In tetrahydrofuran90%
Glycine anhydride
106-57-0

Glycine anhydride

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

1,4-bis(trimethylsilyl)-2,5-piperazinedione
3553-95-5

1,4-bis(trimethylsilyl)-2,5-piperazinedione

Conditions
ConditionsYield
In acetonitrile Reflux; Inert atmosphere;90%
tetraphenylethane-1,2-diol
464-72-2

tetraphenylethane-1,2-diol

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

1-hydroxy-2-trimethylsiloxy-1,1,2,2-tetraphenylethane

1-hydroxy-2-trimethylsiloxy-1,1,2,2-tetraphenylethane

Conditions
ConditionsYield
With pyridine In acetone at 70℃; for 2h;88.3%
lithium acetate. tert-Butyl methyl ether

lithium acetate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))87%
2-chloro-6-amino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-α,β-D-ribofuranosyl]-purine

2-chloro-6-amino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-α,β-D-ribofuranosyl]-purine

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

A

2-chloro-6-amino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine
908006-51-9

2-chloro-6-amino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine

B

2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine
1266098-30-9

2-chloro-6-trimethylsilylamino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-purine

Conditions
ConditionsYield
Stage #1: 2-chloro-6-amino-9-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-α,β-D-ribofuranosyl]-purine; N,O-Bis(trimethylsilyl)trifluoroacetamide In acetonitrile at 60℃; for 3h; Inert atmosphere;
Stage #2: With trifluorormethanesulfonic acid In acetonitrile at 25 - 60℃; for 17h;
A 8.4%
B 86.6%
trimethylsilyl trifluoromethanesulfonate
27607-77-8

trimethylsilyl trifluoromethanesulfonate

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

2-(benzyloxy)ethoxymethyl chloride
31383-67-2

2-(benzyloxy)ethoxymethyl chloride

4,6,8-triaminoimidazo<4,5-e><1,3>diazepine
162009-79-2

4,6,8-triaminoimidazo<4,5-e><1,3>diazepine

1-benzyloxyethoxymethyl-4,6-diamino-8H-8-iminoimidazo[4,5-e][1,3]diazepine triflate salt

1-benzyloxyethoxymethyl-4,6-diamino-8H-8-iminoimidazo[4,5-e][1,3]diazepine triflate salt

Conditions
ConditionsYield
Stage #1: N,O-Bis(trimethylsilyl)trifluoroacetamide; 4,6,8-triaminoimidazo<4,5-e><1,3>diazepine With pyridine In acetonitrile at 20℃;
Stage #2: trimethylsilyl trifluoromethanesulfonate; 2-(benzyloxy)ethoxymethyl chloride In acetonitrile at -45 - 0℃;
86%
piperidine-2,6-dione
1121-89-7

piperidine-2,6-dione

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

N-trimethylsilylglutarimide

N-trimethylsilylglutarimide

Conditions
ConditionsYield
In acetonitrile for 18h; Inert atmosphere; Schlenk technique;86%
In dichloromethane at 20℃; for 2h;
carminomycin
50935-04-1

carminomycin

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

4'-O-trimethylsilylcarminomycin

4'-O-trimethylsilylcarminomycin

Conditions
ConditionsYield
In acetonitrile at 50℃; for 15h;85%
(+)-Daunomycinone
21794-55-8

(+)-Daunomycinone

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

7-O-trimethylsilyldaunomycinone

7-O-trimethylsilyldaunomycinone

Conditions
ConditionsYield
In dichloromethane for 18h; Ambient temperature;85%
sodium carbonate. tert-Butyl methyl ether

sodium carbonate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))84%
(S)-oxalicumone C

(S)-oxalicumone C

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

(S)-2-(2-methoxycarbonylethyl)-3-((1-methoxycarbonyl)-1-((trimethylsilyl)oxy)methyl)-7-methyl-5-((trimethylsilyl)oxy)chromone

(S)-2-(2-methoxycarbonylethyl)-3-((1-methoxycarbonyl)-1-((trimethylsilyl)oxy)methyl)-7-methyl-5-((trimethylsilyl)oxy)chromone

Conditions
ConditionsYield
In benzene-d6 at 65℃; for 96h;83%
2'-O-(t-butyldimethylsilyl)-3'N-debenzoyl-2-m-N3-benzoyl-10-deacetyltaxol

2'-O-(t-butyldimethylsilyl)-3'N-debenzoyl-2-m-N3-benzoyl-10-deacetyltaxol

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

2'-O-(t-butyldimethylsilyl)-3'N-debenzoyl-3'N-isovaleryl-2-debenzoyl-2-m-N3-benzoyl-10-deacetyl-10-O-(trimethylsilyl)taxol

2'-O-(t-butyldimethylsilyl)-3'N-debenzoyl-3'N-isovaleryl-2-debenzoyl-2-m-N3-benzoyl-10-deacetyl-10-O-(trimethylsilyl)taxol

Conditions
ConditionsYield
With lithium hexamethyldisilazane In tetrahydrofuran at -20℃; for 0.166667h; Inert atmosphere;82.6%
potassium carbonate. tert-Butyl methyl ether

potassium carbonate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))81%
2-amino-4-hydroxy-4-methylpentanoic acid
104302-37-6

2-amino-4-hydroxy-4-methylpentanoic acid

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

C15H37NO3Si3
128753-51-5

C15H37NO3Si3

Conditions
ConditionsYield
at 70 - 80℃; for 0.333333h;80%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

2-amino-4-ethyl-4-hydroxyhexanoic acid
123445-56-7

2-amino-4-ethyl-4-hydroxyhexanoic acid

C17H41NO3Si3
128779-82-8

C17H41NO3Si3

Conditions
ConditionsYield
at 70 - 80℃; for 0.333333h;80%
potassium acetate. tert-Butyl methyl ether

potassium acetate. tert-Butyl methyl ether

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene
87751-69-7

rac-(E)-1,3-diphenyl-3-acetoxy-prop-1-ene

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate
177468-91-6

(E)-dimethyl (1,3-diphenylprop-2-en-1-yl)propanedioate

Conditions
ConditionsYield
bis(η3-allyl-μ-chloropalladium(II))80%
bis(η3-allyl-μ-chloropalladium(II))27%
3'-N-trifluoroacetyldaunorubicin
26388-52-3

3'-N-trifluoroacetyldaunorubicin

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

3'-N-trifluoroacetyl-4'-O-trimethylsilyldaunorubicin

3'-N-trifluoroacetyl-4'-O-trimethylsilyldaunorubicin

Conditions
ConditionsYield
In acetonitrile for 24h;76%
guaiol
489-86-1

guaiol

N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

{2-[(3S,5R,8S)-3,8-dimethyl-1,2,3,4,5,6,7,8-octahydroazulen-5-yl]-propan-2-yl-oxy}(trimethyl)silane

{2-[(3S,5R,8S)-3,8-dimethyl-1,2,3,4,5,6,7,8-octahydroazulen-5-yl]-propan-2-yl-oxy}(trimethyl)silane

Conditions
ConditionsYield
With 1,1,1,2,2,2-hexamethyldisilane; magnesium bromide ethyl etherate at 20℃; Inert atmosphere;73%
N,O-Bis(trimethylsilyl)trifluoroacetamide
25561-30-2

N,O-Bis(trimethylsilyl)trifluoroacetamide

(4R,5R,8R,9S,10R,13S,14S,17S)-17-Hydroxy-13-methyl-tetradecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-one
3941-50-2

(4R,5R,8R,9S,10R,13S,14S,17S)-17-Hydroxy-13-methyl-tetradecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-one

3,17β-bis(trimethylsilyloxy)-4,5β-epoxyestr-2-ene
85382-37-2

3,17β-bis(trimethylsilyloxy)-4,5β-epoxyestr-2-ene

Conditions
ConditionsYield
for 48h; Heating;70%

25561-30-2Relevant articles and documents

Carbacephalosporin compound, their preparation and use

-

, (2008/06/13)

Carbacephalosporin compounds of formula (I), STR1 salts thereof, processes for their synthesis and uses thereof, wherein: R1 is hydrogen, methoxy or formamido; R2 is an acyl group; CO2 R3 is a carboxy group or a carboxylate anion, or R3 is a carboxy protecting group or a pharmaceutically acceptable salt-forming group or in vivo hydrolysable ester group; R4, R5, R6 and R7 represent hydrogen or a substituent; R4 and R7 may be replaced by a chemical bond between the two carbon atoms shown; R5 and R6 may be linked together into a cyclic system. The compounds (I) have antibacterial properties.

Bis-trimethylsilyl cefamandole and process therefor

-

, (2008/06/13)

Bis-trimethylsilyl cefamandole is useful for regenerating cefamandole of excellent purity.

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