Best price ,Best quality,ship on time Appearance:colorless liquid Storage:should not be stored for a long time Package:70kgs drum Application:synthetic chemistry reagent for cleaving ethers,esters,carbamates,ketals,and lactones. Port:qingdao,shang
GOLDEN PHARMA CO.,LIMITED.is a professional pharmaceutical company,our team have more than 20years expereince in pharmaceutical production and sales. we are a professional technical enterprise specializing in the R & D, production,QA regulation
Specificaiton: In-house; Certification: ISO 9001; US FDA and EDQM Approved Plant Appearance:Colorless to light red transparent liquid Storage:Preserve in ambient temperature Application:Efficient reagent for ether, ester, carbamate, ketal, and la
Dayangchem's 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. DayangChem can provide different quantities
Cas:16029-98-4
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Min.Order:70 Kilogram
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inquiryhigh quality Appearance:Liquid Storage:Sealed, dry, microtherm , avoid light and smell Package:According to the demand of customer Application:Pharmaceutical intermediates Transportation:by air or by sea Port:shanghai
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
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Min.Order:5 Kiloliter
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Type:Manufacturers
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Iodotrimethylsilane Synonym: Trimethylsilyl iodide; TMS iodide; Trimethyliodosilane; Tri methyl silyl iodide CAS No.:16029-98-4 Molecular formula:(CH3)3SiI Molecular Weight:200.1 Properties: water clear to pinkish-red l
We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
Cas:16029-98-4
Min.Order:1 Gram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
Negotiable
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inquiryProduct Name: Iodotrimethylsilane CAS: 16029-98-4 MF: C3H9ISi MW: 200.09 EINECS: 240-171-0 Mol File: 16029-98-4.mol Iodotrimethylsilane Structure Iodotrimethylsilane Chemical Properties Melting point <0°C Boiling point
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Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryOur company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
Cas:16029-98-4
Min.Order:1 Kilogram
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inquiryIodotrimethylsilane CAS:16029-98-4 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic inter
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Min.Order:1 Gram
Negotiable
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Cas:16029-98-4
Min.Order:1 Kilogram
Negotiable
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inquiry16029-98-4 Iodotrimethylsilane Molecular formula:(CH3)3SiI Molecular Weight:200.1 Properties:water clear to pinkish-red liquid Technical Specifications: Density(20℃)g/cm3 1.406 Content of Iodotrimethylsilane ≥99.0% Appearance:water c
Product Detail Minimum Order Qty. 10 Gram
Cas:16029-98-4
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryAppearance:off-white to white solid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for Synthesis API and Research Transportation:As customer request Port:Qingda
Cas:16029-98-4
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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
Cas:16029-98-4
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
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
Our Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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Min.Order:10 Gram
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Type:Lab/Research institutions
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We are one of a few suppliers that can offer custom synthesis service of this product We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are committed to prov
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Type:Lab/Research institutions
inquiryHexamethyldisiloxane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With phosphorus; iodine at 80℃; for 10h; Temperature; Inert atmosphere; | 99% |
With iodine; aluminium at 55 - 130℃; for 2h; Concentration; Temperature; Inert atmosphere; | 93.9% |
With iodine; aluminium | 66% |
chloro-trimethyl-silane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide; lithium iodide at 60℃; for 10h; Temperature; Reagent/catalyst; Inert atmosphere; | 98.56% |
With lithium iodide for 4h; Ambient temperature; | 88% |
With magnesium iodide In xylene Heating; |
phenyl trimethylsilyl selenide
A
trimethylsilyl iodide
B
diphenyl diselenide
Conditions | Yield |
---|---|
With iodine | A 98% B 96% |
1,1,1,2,2,2-hexamethyldisilane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With iodine at 65 - 130℃; for 2h; | 96.1% |
With iodine In dichloromethane Thermodynamic data; Kinetics; ΔS(excit.), ΔG(excit.), ΔE(excit.); | |
With iodine |
pentamethylcyclopentadienyltrimethylsilane
titanium(IV) iodide
B
trimethylsilyl iodide
Conditions | Yield |
---|---|
In toluene Dropwise addn. of TiI4 in toluene to soln. of C(CH3)5Si(CH3)3 in toluene, stirring (2 h, color change from red to dark-red), reflux (1 h); Evapn. of solvent and byproduct (vacuum), washing of crystals (pentane), dried (vacuum), elem. anal.; | A 95.2% B n/a |
bis(trimethylsilyl)selenide
trimethylsilyl iodide
Conditions | Yield |
---|---|
With iodine In m-xylene | 94% |
trimethylphenylsilane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With I2; AlI3 | 93% |
With I2 | 56% |
With aluminium(III) iodide; iodine | |
With iodine |
potassium ethyl xanthogenate
methyl iodide
A
trimethylsilyl iodide
B
O-ethyl S-methyl dithiocarbonate
Conditions | Yield |
---|---|
In acetone | A n/a B 90% |
tetrakis(trimethylsiloxy)phosphonium iodide
A
trimethylsilyl iodide
B
Tris(trimethylsilyl) phosphate
Conditions | Yield |
---|---|
In benzene Heating; during 5 h the solvent was distilled off, the temp. rose to 110 deg C; | A n/a B 85% |
N,N-diethyl-1,1,1-trimethylsilanamine
trimethylsilyl iodide
Conditions | Yield |
---|---|
With iodine In neat (no solvent) for 15h; Ambient temperature; | 85% |
octamethylcyclotetrasiloxane
A
trimethylsilyl iodide
B
Hexamethyldisiloxane
C
methyl iodide
Conditions | Yield |
---|---|
With aluminium(III) iodide at 140 - 170℃; for 5h; | A n/a B 83.5% C n/a |
1,1,3,3-Tetramethyldisiloxane
Hexamethyldisiloxane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With iodine for 0.166667h; Heating; | 80% |
Conditions | Yield |
---|---|
76% |
acetyl iodide
tris(trimethylsilyl)amine
A
trimethylsilyl iodide
B
N,N-bis(trimethylsilyl)acetamide
Conditions | Yield |
---|---|
at 60 - 70℃; for 6h; | A 65% B 53% |
octamethylcyclotetrasiloxane
A
tetramethylsilane
B
trimethylsilyl iodide
C
Hexamethyldisiloxane
D
tetradecamethylhexasiloxane
Conditions | Yield |
---|---|
With gallium(III) iodide at 140 - 170℃; for 5h; Yields of byproduct given; | A 61% B n/a C n/a D n/a |
With gallium(III) iodide at 140 - 170℃; for 5h; Title compound not separated from byproducts; | A 61% B n/a C n/a D n/a |
With gallium(III) iodide at 140 - 170℃; for 5h; Yield given; Title compound not separated from byproducts; | A 61% B n/a C n/a D n/a |
octamethylcyclotetrasiloxane
A
tetramethylsilane
B
trimethylsilyl iodide
C
Hexamethyldisiloxane
D
dodecamethyl-cyclohexasiloxane
Conditions | Yield |
---|---|
With gallium(III) iodide at 140 - 170℃; for 5h; Yield given; Title compound not separated from byproducts; | A 61% B n/a C n/a D n/a |
octamethylcyclotetrasiloxane
A
tetramethylsilane
B
trimethylsilyl iodide
C
Hexamethyldisiloxane
D
hexadecamethylheptasiloxane
Conditions | Yield |
---|---|
With gallium(III) iodide at 140 - 170℃; for 5h; Yield given; Title compound not separated from byproducts; | A 61% B n/a C n/a D n/a |
acetyl iodide
N,N-bis(trimethylsilyl)ethanamine
A
trimethylsilyl iodide
B
N-trimethylsilyle du N-ethylacetamide
Conditions | Yield |
---|---|
at 60 - 70℃; for 8h; | A 23% B 61% |
phenyltrimethylsilyl ether
A
tetramethylsilane
B
trimethylsilyl iodide
C
Hexamethyldisiloxane
D
methyl iodide
Conditions | Yield |
---|---|
With gallium(III) iodide at 175 - 180℃; for 3h; | A 60% B n/a C n/a D n/a |
With gallium(III) iodide at 175 - 180℃; for 3h; Title compound not separated from byproducts; | A 60% B n/a C n/a D n/a |
tris(trimethylsilyl)amine
benzoyl iodide
A
trimethylsilyl iodide
B
N,N-bis(trimethylsilyl)benzamide
Conditions | Yield |
---|---|
at 120 - 130℃; for 8h; | A 59% B 32% |
1-Iodonaphthalene
ethenyltrimethylsilane
A
1-vinylnaphthalene
B
propene
C
ethene
D
trimethylsilyl iodide
E
Hexamethyldisiloxane
F
buta-1,3-diene
Conditions | Yield |
---|---|
bis(η3-allyl-μ-chloropalladium(II)) In water; N,N-dimethyl-formamide at 100℃; for 5h; Product distribution; other aromatic halides: α-bromonaphthalene, α-halopyridines, iodobenzene, p-substituted iodobenzenes; 9-iodo-m-carborane; other catalysts: (Ph3P)4Pd, LiPdCl3, (PhCN)2PdCl2, (MeCN)2PdCl2, Pd/C; Et3N presence; other solvent: hexametapol; | A 55% B n/a C n/a D n/a E n/a F n/a |
Conditions | Yield |
---|---|
Heating; | A 53% B 13% |
Conditions | Yield |
---|---|
at 116℃; for 12h; | 48% |
N,N-bis(trimethylsilyl)ethanamine
benzoyl iodide
A
trimethylsilyl iodide
B
N-ethyl-N-trimethylsilylbenzamide
Conditions | Yield |
---|---|
at 80 - 104℃; for 13h; | A 36% B 25% C 9.86 g |
S-trimethylsilyl O-ethyldithiocarbonate
methyl iodide
A
trimethylsilyl iodide
B
O-ethyl S-methyl dithiocarbonate
Conditions | Yield |
---|---|
In chloroform-d1 for 24h; | A n/a B 30% |
1-chloro-1,1,3,3,3-pentamethyldisiloxane
A
trimethylsilyl iodide
B
octamethylcyclotetrasiloxane
C
1-chloroheptamethyltrisiloxane
D
1-chloro-1,1,3,3,5,5,7,7,7-nonamethyltetrasiloxane
Conditions | Yield |
---|---|
With sodium iodide In acetonitrile for 18h; Mechanism; Ambient temperature; other siloxanes; other reagent, var. temp.; | A 14% B 10% C n/a D n/a |
Conditions | Yield |
---|---|
at 80℃; | |
at 80℃; |
hexamethyldisilathiane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With 1-Iodoheptane at 160℃; | |
With dibutyl-iodo-borane In carbon disulfide |
n-butylthiotrimethylsilane
trimethylsilyl iodide
Conditions | Yield |
---|---|
With diiodomethane |
Conditions | Yield |
---|---|
at 80℃; | 100% |
4-methyl-1,3-dioxane
trimethylsilyl iodide
A
Hexamethyldisiloxane
B
3-Iodo-1-iodomethoxy-butane
C
1-Iodo-3-iodomethoxy-butane
Conditions | Yield |
---|---|
at 70℃; for 3.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; | A 100% B n/a C n/a |
Conditions | Yield |
---|---|
at 100℃; | 100% |
cis,trans-2,5-dimethoxytetrahydrofuran
trimethylsilyl iodide
1,4-Diiodo-1,4-dimethoxy-butane
Conditions | Yield |
---|---|
100% |
cis- and trans-2,6-Dimethoxytetrahydropyran
trimethylsilyl iodide
1,5-Diiodo-1,5-dimethoxy-pentane
Conditions | Yield |
---|---|
100% |
trimethylsilyl iodide
trimethylsiloxydiethylphosphinate
bis(trimethylsilyloxy)diethylphosphonium iodide
Conditions | Yield |
---|---|
In benzene | 100% |
trimethylsilyl iodide
trimethylsiloxydipropylphosphinate
bis(trimethylsilyloxy)dipropylphosphonium iodide
Conditions | Yield |
---|---|
In benzene | 100% |
trimethylsilyl iodide
(methoxyethynyl)bis(pentafluorophenyl)phosphine
(trimethylsilyl)ketene
Conditions | Yield |
---|---|
In nitromethane at 20℃; for 2h; | 100% |
trimethylsilyl iodide
Ethoxyethynyl-bis-pentafluorophenyl-phosphane
(trimethylsilyl)ketene
Conditions | Yield |
---|---|
In nitromethane at 20℃; for 2h; | 100% |
trimethylsilyl iodide
ethyl P-(diethoxymethyl)phosphonite
Conditions | Yield |
---|---|
In dichloromethane for 1.5h; | 100% |
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