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inquiryItems Standard Result Appearance Colorless liquid Pass Assay ≥99.0% 99.
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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inquiryProduct Description Product Name Trifluoroacetic anhydride CAS No. 407-25-0 Appearance Coloress transparent liquid Assay ≥99.5% Capacity 500mt/year Packing
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
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inquiryISO Certification Technology: Technology innovation is our eternal pursuit,or we will be left behind.Our technology experts,all from famous universities and institutes,has rich experience and high achievements in chemical research.This makes sure
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The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Our company is engaged in customizing the benzene ring and pyridine derivative organic intermediates, and the quantity is flexible according to customer's needs. It mainly provides high-quality intermediates for domestic and foreign pharmaceuti
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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inquiryOur company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so
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inquiryProduct name Trifluoroacetic anhydride Synonyms 2,2,2-Trifluoroacetic anhydride CAS No. 407-25-0 EINECS No. 206-982-9 Molecular Formula
1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Powder Storage:Store in sealed conta
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Lorcaserin(856681-05-5)is an orally administered agent and a selective 5-HT2C receptor agonist for the treatment of obesity. It had been approved for marketing in US by FDA on 27 June in 2012. In clinical studies, lorcaserin h
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiry407-25-0 99%Appearance:white powder Storage:keep cold Package:according to customers' requirements Application:Pharmaceutical intermediates 407-25-0 Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF or CNF ect...)or accord
Superior quality Appearance:Clear, colorless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application: Used as analytical reagents, solvents, cataly
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inquiryProduct name: Trifluoroacetic Anhydride CAS No.: 407-25-0 Molecule Formula:C4F6O3 Molecule Weight:210.03 Purity: 99.0% Package: 200kg/drum Description:Colorless clear liquid Manufacture Standards:Enterprise Standard
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryHANGZHOU THINK CHEMICAL CO., LTD. (THINKCHEM) is an integrative corporation of trade, research and contract manufacture. With about ten years of business experiences on the marketing & distribution, thinkchem specializes in exp
Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting Trifluoroacetic Anhydride ;TFAA 99%CAS:407-25-0, Please contact us by email freely. We are leading exporter in China. If you really
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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an
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SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in custom synthe
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryN-(n-butyl)-2,4-dinitrotrifluoroacetanilide
A
2,4-dinitro-N-butylaniline
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
With tris buffers; cetyltrimethylammonim bromide at 25℃; Rate constant; hydrolysis, other quaterner amines; | A 99.7% B n/a |
Conditions | Yield |
---|---|
With fuming sulphuric acid at 130℃; Large scale; | 99% |
With fuming sulphuric acid at 78 - 130℃; Large scale; | 99% |
With sulfuric acid; sulfur trioxide at 130℃; | 99% |
trifluoromethyldiiodophosphine
silver trifluoroacetate
A
Trifluormethylphosphonigsaeure-bis(trifluoressigsaeure)anhydrid
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
within 10 h; | A n/a B 98% |
10 min; isolation from volatile part of product; | A n/a B 72% |
trifluorormethanesulfonic acid
trifluoroacetic acid
A
trifluoroacetic anhydride
B
trifluoroacetyl triflate
Conditions | Yield |
---|---|
With phosphorus pentoxide at -20 - 240℃; for 3.5h; | A n/a B 75% |
Cl2SNTeF5
silver trifluoroacetate
A
F5TeNSO
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
In neat (no solvent) Cl2S=NTeF5 and CF3COOAg stirred at room temp. and warmed to 45°Cand stirred for 1 h; O=S=NTeF5 and (CF3CO)2O condensed into -196°C trap under vac., separation achieved by trap-to-trap distillation through -45 (O=S=NTeF5) and -78°C cooled traps; elem. anal.; | A 68% B n/a |
2,2,2-trifluoroethyl trifluoroacetate
A
Carbonyl fluoride
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
With chlorine at 22.84℃; under 760 Torr; Irradiation; Synthetic gas; | A 35% B 45% |
mercury(II) trifluoroacetate
chloro(chlorosulfanyl)methanone
trifluoroacetic anhydride
Conditions | Yield |
---|---|
at 50 - 55℃; for 3h; | 30% |
O,O-Diethyl O-Trifluoroacetyl Phosphate
A
Tetraethyl pyrophosphate
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Erhitzen im Vakuum; |
tris(trifluoro acetyloxy)borane
A
tetrakis-trifluoroacetoxy-diboroxane
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
at 100℃; under 0.0001 Torr; | |
at 100℃; under 0.0001 Torr; |
Conditions | Yield |
---|---|
With phosphorus at 180℃; | |
With sulfur at 300℃; |
calcium bistrifluoroacetate
A
trifluoroacetyl fluoride
B
trifluoroacetic anhydride
trifluoroacetic acid
A
trifluoroacetyl fluoride
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Erhitzen des Lithium-Salzes; |
Bis(trifluormethyl)phosphinigsaeure-trifluoressigsaeureanhydrid
A
Tetrakis(trifluormethyl)disphosphoxan
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
at 40℃; Equilibrium constant; | |
within 24 h; | |
equil.; |
trifluoromethyl isocyanide
trifluoroacetic acid
A
N-(trifluoromethyl)formamide
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Ambient temperature; Yield given. Yields of byproduct given; |
trifluoroacetic acid
trifluoroacetyl triflate
A
trifluorormethanesulfonic acid
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Equilibrium constant; |
N-Allyl-9-anthracenemethanimine
A
2-(Trifluoroacetyl)-1,2,3,3a,4,5-hexahydro-5,9b-o-benzenobenzisoindol-1-ol
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
In dichloromethane for 24h; Ambient temperature; Title compound not separated from byproducts; |
3,6-dehydrohomoadamantane
chromyl trifluoroacetate
A
trifluoroacetic anhydride
Conditions | Yield |
---|---|
In tetrachloromethane at 0℃; for 0.5h; | A 17 % Spectr. B 34 % Spectr. C 42 % Spectr. |
Caesium; 2,3,3,3-tetrafluoro-2-methoxy-propionate
A
Carbonyl fluoride
B
trifluoroacetyl fluoride
C
methyl 1,2,2-trifluorovinyl ether
D
2-fluoro-2-methoxy trifluoropropanoic acid methyl ester
E
α-methoxytetrafluoropropionyl fluoride
F
trifluoroacetic anhydride
Conditions | Yield |
---|---|
at 250℃; under 0.01 Torr; for 1.5h; Product distribution; Mechanism; |
iodine
silver trifluoroacetate
benzene
A
iodobenzene
B
trifluoroacetic anhydride
iodo-bis-trifluoromethyl-phosphine
silver trifluoroacetate
A
Bis(trifluormethyl)phosphinigsaeure-trifluoressigsaeureanhydrid
B
Tetrakis(trifluormethyl)disphosphoxan
C
trifluoroacetic anhydride
Conditions | Yield |
---|---|
byproducts: AgI; below 20°C; further react. in equil.; distn.; main product as medium fraction at 0°C / 55 Torr; |
Trifluormethylphosphonigsaeure-bis(trifluoressigsaeure)anhydrid
A
Tetrakis(trifluormethyl)disphosphoxan
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
18.5 degree.C; equil.; value for equil. const. given at 40°C; |
Trifluormethylphosphonigsaeure-bis(trifluoressigsaeure)anhydrid
trifluoroacetic anhydride
Conditions | Yield |
---|---|
With (CH3)3N formation from unidentified intermediate product; |
A
yttrium(III) fluoride
B
carbon dioxide
C
carbon monoxide
D
trifluoroacetic anhydride
Conditions | Yield |
---|---|
With O2 or Ar In neat (no solvent) decompn. at 300 ° C in Ar and at 230-270 ° C in O2; YF3 formed; |
Conditions | Yield |
---|---|
In neat (no solvent) pyrolysis at 240°C within 24 hours;; |
ethyl trifluoroacetate,
hydrazine
A
1,2-bis(trifluoroacetyl)hydrazine
B
trifluoroacetic acid
C
trifluoroacetic anhydride
Conditions | Yield |
---|---|
In ethanol dropping of soln. of CF3COOC2H5 in abs. alc. to N2H4 soln. in anhydrous C2H5OH by cooling, stirring at 20°C (12 h); evapn. of C2H5OH, stirring at 20°C (12 h); |
S-trifluoromethylcarbonothioic trifluoroacetic anhydride
S,S'-Bis(trifluormethyl)dithiocarbonat
B
trifluoroacetic anhydride
Conditions | Yield |
---|---|
Irradiation (UV/VIS); photolysis; | |
Irradiation (UV/VIS); photolysis; |
Trifluoromethyliodine(III) bis-trifluoroacetate
A
iodotrifluoromethane
B
trifluoromethyliodine dioxide
C
trifluoroacetic anhydride
Conditions | Yield |
---|---|
above -6°C; |
Conditions | Yield |
---|---|
100% | |
With benzene | |
With 1H-imidazole |
4-chloro-aniline
trifluoroacetic anhydride
N-(4-chlorophenyl)-2,2,2-trifluoroacetamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h; | 100% |
With triethylamine In dichloromethane at 0 - 20℃; for 2h; | 88% |
In diethyl ether for 1h; Ambient temperature; | 84% |
4-methoxy-aniline
trifluoroacetic anhydride
2,2,2-trifluoro-N-(4-methoxy-phenyl)-acetamide
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 20℃; | 100% |
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h; | 100% |
at 20℃; for 1h; | 98.3% |
isopropylamine
trifluoroacetic anhydride
2,2,2-trifluoro-N-(1-methylethyl)acetamide
Conditions | Yield |
---|---|
With pyridine; dmap In tetrahydrofuran at 20℃; for 15h; | 100% |
With diethyl ether | |
In diethyl ether | |
at 0℃; than Rt, 3 h; | |
In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; Glovebox; |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 8h; | 100% |
at 100℃; Cooling with ice; | 93% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 0.166667h; | 100% |
With erbium(III) chloride for 2h; Heating; | 99% |
In diethyl ether at 0℃; for 2h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With water-d2 at -78℃; | 100% |
With water-d2 | |
With water-d2 1.) 0 deg C, 2.) reflux, 30 min; |
m-Anisidine
trifluoroacetic anhydride
N-(3-methoxyphenyl)-2,2,2-trifluoroacetamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h; | 100% |
In diethyl ether | |
With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere; | |
With triethylamine | |
at 20℃; for 3h; Inert atmosphere; |
2-methoxy-phenylamine
trifluoroacetic anhydride
N-(2-methoxyphenyl)-2,2,2-trifluoro-acetamide
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 0.75h; | 100% |
With pyridine In dichloromethane at 0 - 20℃; for 72h; Inert atmosphere; | 99% |
In diethyl ether | |
Stage #1: 2-methoxy-phenylamine With pyridine In dichloromethane at 0℃; for 0.5h; Stage #2: trifluoroacetic anhydride In dichloromethane at 0 - 30℃; for 1.25h; | |
With pyridine In dichloromethane at 0 - 20℃; for 1.25h; |
anthranilic acid
trifluoroacetic anhydride
2-trifluoromethyl-4H-3,1-benzoxazin-4-one
Conditions | Yield |
---|---|
In neat (no solvent) at 130℃; for 6h; Sealed tube; Inert atmosphere; | 100% |
In chloroform for 1h; Reflux; | 56% |
In ethyl acetate |
2,3-Dimethylaniline
trifluoroacetic anhydride
N-(2,3-dimethylphenyl)-2,2,2-trifluoroacetamide
Conditions | Yield |
---|---|
In dichloromethane for 1h; Further stages; | 100% |
With triethylamine In dichloromethane for 1h; Ambient temperature; | 87% |
In diethyl ether | |
In dichloromethane at 0 - 20℃; for 12h; |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 4h; | 100% |
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane at 0℃; for 0.333333h; | 100% |
L-cystine dimethyl ester dihydrochloride
trifluoroacetic anhydride
N,N'-bis(trifluoroacetyl)-L-cystine dimethyl ester
Conditions | Yield |
---|---|
With trifluoroacetic acid at -5 - 20℃; | 100% |
In trifluoroacetic acid Ambient temperature; | 98% |
90% | |
In trifluoroacetic acid |
1-indoline
trifluoroacetic anhydride
2,2,2-trifluoro-1-(indolin-1-yl)ethan-1-one
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 100% |
In dichloromethane at 0℃; for 1h; Inert atmosphere; | 100% |
In benzene at 0 - 5℃; | 96% |
1,2,3,4-tetrahydroisoquinoline
trifluoroacetic anhydride
1-(3,4-dihydroquinolin-1(2H)-yl)-2,2,2-trifluoroethanone
Conditions | Yield |
---|---|
With triethylamine In diethyl ether at 0 - 20℃; for 5h; | 100% |
With triethylamine In diethyl ether at 20℃; for 5h; | 100% |
With triethylamine In diethyl ether at 0 - 20℃; | 98% |
4,6-di-O-acetyl-3-O-methyl-D-glucal
trifluoroacetic anhydride
Trifluoro-acetic acid (4R,5S,6R)-5-acetoxy-6-acetoxymethyl-4-methoxy-3-nitro-tetrahydro-pyran-2-yl ester
Conditions | Yield |
---|---|
With ammonium nitrate for 1h; | 100% |
Conditions | Yield |
---|---|
In benzene 1) 0 degC, 3 h, 2) 20 degC, 1 h; | 100% |
1-(3-aminophenyl)ethanone
trifluoroacetic anhydride
3-trifluoroacetamidoacetophenone
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0℃; for 0.5h; | 100% |
In N,N-dimethyl-formamide for 48h; Ambient temperature; | 80% |
With trifluoroacetic acid Heating; |
3-trifluoromethylaniline
trifluoroacetic anhydride
2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetamide
Conditions | Yield |
---|---|
With triethylamine In 2-methyltetrahydrofuran | 100% |
Stage #1: 3-trifluoromethylaniline; trifluoroacetic anhydride With pyridine In dichloromethane at 0 - 20℃; Stage #2: With sodium hydrogencarbonate In dichloromethane | 98% |
In N,N-dimethyl-formamide for 48h; Ambient temperature; | 70% |
With triethylamine In tetrahydrofuran at 0 - 20℃; | 51.1% |
In dichloromethane |
Conditions | Yield |
---|---|
for 0.5h; | 100% |
2-(5,8-Dimethoxy-quinolin-4-yl)-phenylamine
N-ethyl-N,N-diisopropylamine
trifluoroacetic anhydride
N-[2-(5,8-Dimethoxy-quinolin-4-yl)-phenyl]-2,2,2-trifluoro-acetamide
Conditions | Yield |
---|---|
at 0℃; for 0.5h; | 100% |
3-nitro-aniline
trifluoroacetic anhydride
N-trifluoroacetic-3-nitroaniline
Conditions | Yield |
---|---|
In pyridine; dichloromethane | 100% |
With pyridine In dichloromethane at 20℃; for 3h; | 95% |
In acetonitrile for 2h; Ambient temperature; |
4-Methyl-2H-1,4-thiazin-3-one
trifluoroacetic anhydride
6-Trifluoroacetyl-4-methyl-2H-1,4-thiazin-3-one
Conditions | Yield |
---|---|
With pyridine In chloroform for 1080h; Ambient temperature; | 100% |
2-methyl-8-nitroindolizine
trifluoroacetic anhydride
2,2,2-Trifluoro-1-(2-methyl-8-nitro-indolizin-3-yl)-ethanone
Conditions | Yield |
---|---|
100% |
1,2-O-isopropylidene-3-amino-3,5-dideoxy-α-D-ribofuranoside
trifluoroacetic anhydride
3,5-dideoxy-3-(trifluoroacetamido)-1,2-O-isopropylidene-α-D-ribofuranose
Conditions | Yield |
---|---|
In diethyl ether 1.) 0 deg C, 0.5 h, 2.) RT, 30 min; | 100% |
N,N-dimethyl-1-naphthalenamine
trifluoroacetic anhydride
N,N-Dimethyl-2,4-bis(trifluoroacetyl)-1-naphthylamine
Conditions | Yield |
---|---|
With pyridine In chloroform for 18h; Ambient temperature; | 100% |
With pyridine In chloroform for 19h; Ambient temperature; 2.5 eq. (CF3CO)2O; |
2,3,4,6-tetra-O-benzyl-D-glucopyranose
trifluoroacetic anhydride
2,3,4,6-tetra-O-benzyl-1-O-(trifluoroacetyl)-α-D-glucopyranose
Conditions | Yield |
---|---|
With sodium 2,2,2-trifluoroacetate for 0.5h; Heating; | 100% |
3,4,6-tri-O-acetyl-D-glucal
trifluoroacetic anhydride
Trifluoro-acetic acid (4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-nitro-tetrahydro-pyran-2-yl ester
Conditions | Yield |
---|---|
With ammonium nitrate for 1h; | 100% |
Conditions | Yield |
---|---|
erbium(III) triflate In acetonitrile at 20℃; for 2.5h; | 100% |
With erbium(III) chloride for 1.5h; Heating; | 99% |
With triethylamine In benzene at 25 - 30℃; for 1h; |
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