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Henan 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
Product Name: cyanic acid Synonyms: Cyanate;C01417 CAS: 71000-82-3 MF: CHNO MW: 0 EINECS:
Cas:71000-82-3
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:71000-82-3
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryWe are a Union of chemistry in China, consists of chemists,engineers, laboratories,factories in China. We organize surplus capacity of R&D and production as well as custom synthesis for chemical products and chemical business project. We are supp
Our own factory produces direct sales with absolute price advantage Application:Pharmaceutical industry Transportation:By sea Port:Shanghai/tianjin
We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white to yellow crystal powder Storage:Room temperature with sealed well Package:according to the clients requirement Applicatio
1. Timely and efficient service to ensure communication with customers2. Produce products of different specifications and sizes according to your requirements.3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures sta
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
The company have effective management team, professional technical R & D personnel, the service spirit of customer oriented. We have long-term cooperation with famous domestic manufacturer, and excellent customer resources overseas. We are skilled in
cyanide(1-)
cyanate
Conditions | Yield |
---|---|
With 4,40-Di-tert-butyl-2,20-bipyridine; dihydrogen peroxide In N,N-dimethyl-formamide at 20℃; for 2.5h; Catalytic behavior; Kinetics; Reagent/catalyst; | 100% |
With alkali peroxide In not given in alkaline soln.;; | |
With chlorine In water byproducts: Cl(1-); introduction of Cl2 into alkali cyanide soln.; |
Conditions | Yield |
---|---|
With oxygen at 24.9℃; under 0.4 Torr; Product distribution; various neutral molecules with or without acidic hydrogen; |
methyl isocyanate
A
methyl hydroperoxide
B
cyanide(1-)
C
cyanate
Conditions | Yield |
---|---|
With hydroperoxide anion In gaseous matrix at 26.9℃; Rate constant; Product distribution; in a flowing afterglow system (flow rector affixed to a quadrupole mass spectrometer); |
Thiocyanate
cyanate
Conditions | Yield |
---|---|
With {Ni(OH)2(H3IO6)2}(2-) Kinetics; byproducts: SO4(2-), H2O; oxidation in aq. alkaline medium, pH=8-10; |
Thiocyanate
chlorite
water
A
cyanate
B
chloride
C
Sulfate
Conditions | Yield |
---|---|
In perchloric acid Kinetics; 25°C, ionic strength 0.5 M (NaClO4); not isolated; UV/VIS monitoring (360 nm); |
Conditions | Yield |
---|---|
With chloramine-B or bromamine-B In water Kinetics; byproducts: SO4(2-); oxidation of thiocyanate ion by chloramine-B or bromamine-B in alkaline medium (293-323 K) for 24 h; |
Conditions | Yield |
---|---|
In water pH=11-12; | |
In water pH=11-12; |
Conditions | Yield |
---|---|
In water byproducts: (CONH2)2; reduction of Tl(III) oxide with HCN in H2O; NMR; |
Conditions | Yield |
---|---|
In water Kinetics; izomerization; | |
thermal decompn.; identified by IR; |
Conditions | Yield |
---|---|
With sodium hydroxide In water Kinetics; basic hydrolysis of cyanogen iodide at room temp.; monitored by UV-spectroscopy of the I(1-) species; |
sodium cyanide
cyanate
Conditions | Yield |
---|---|
In water Electrolysis; electrolysis with Pt electrode at anodic potenitals at 0.15 V in pH 12 soln.; mechanism discussed;; detn. by IR;; |
sodium cyanide
dihydrogen peroxide
sodium hydroxide
A
cyanate
B
copper hydroxide
Conditions | Yield |
---|---|
In water Kinetics; addn. of H2O2 to soln. of other educts (pH = 10); |
Conditions | Yield |
---|---|
With air In solid heated to 490 ° C in static air atm at heating rate 5 °/min (TG/DSC expt.);; detected by IR;; |
A
cyanate
B
carbonate(2-)
Conditions | Yield |
---|---|
With air In solid heated to 350 ° C in static air atm at heating rate 5 °/min (TG/DSC expt.);; detected by IR;; |
Conditions | Yield |
---|---|
With air In solid heated to 300 ° C in static air atm at heating rate 5 °/min (TG/DSC expt.);; detected by IR;; |
Conditions | Yield |
---|---|
With catalyst Pd/Al2O3 In neat (no solvent) byproducts: H(1+); exposing a Pd/Al2O3 catalyst to 15 Torr of a CO/NH3 mixt. (2:1) at 298 K for 30 min; detd. by IR spectroscopy; | |
formation of surface isocyanate on iron surface (silica-supported iron catalyst) from coadsopted CO/NH3 mixt. at 298-523 K; IR; |
Conditions | Yield |
---|---|
equiv. amts. of educts; | |
equiv. amts. of educts; |
Conditions | Yield |
---|---|
In neat (no solvent, gas phase) byproducts: H2O, OH(1-); in flowing afterglow system at 298 K, at 0,3-0.4 torr and 140-190 cm3/s He.; |
Conditions | Yield |
---|---|
byproducts: formate, carbonate; | |
byproducts: formate, carbonate; |
methyl isocyanate
hydroperoxide anion
A
cyanide(1-)
B
hydroxyl
C
cyanate
Conditions | Yield |
---|---|
In gas Kinetics; byproducts: CH3NCO2(1-), (CH4O3), CH3O2H; gas-phase react. of hydroperoxide with CH3NCO; not isolated; detn. by mass spectroscopy;; |
Conditions | Yield |
---|---|
in high-frequency spark; identified by MS; |
Conditions | Yield |
---|---|
In water at pH = 8.5 - >10;; |
Conditions | Yield |
---|---|
In water in alkaline soln.; | |
In water in alkaline soln.; |
Conditions | Yield |
---|---|
In water Kinetics; byproducts: SO4(2-), H2O, OH(1-); UV, IR; |
cyanate
Conditions | Yield |
---|---|
In tetrahydrofuran to complex in THF was added anion; water was added, product was extracted into CH2Cl2, crystd. upon the addition Et2O; | 90% |
cyanate
Conditions | Yield |
---|---|
In tetrahydrofuran to complex in THF was added anion; water was added, product was extracted into CH2Cl2, crystd. upon the addition Et2O; | 90% |
cyanate
N,N-dimethylethylenediamine
[Cu(N3)(NCO)(N,N-dimethylethylenediamine)]2
Conditions | Yield |
---|---|
In methanol; water aq. soln. of NaN3, NCO(1-) added to soln. of Cu(NO3)2*3H2O and org. ligand in MeOH; mixt. stirred for 30 min at 299 K; filtered; washed (Et2O); dried (vac.); elem. anal.; | 70% |
Conditions | Yield |
---|---|
In tetrahydrofuran NaNCO or KNCO was added to a THF soln. of Nb-compound in 2:1 ratio under anhyd. conditions, mixt. was stirred and refluxed for ca. 12 h at 65-70°C; filtered, ppt. was washed with THF, filtrate and washings were evapd. in vacuo (2 h), residue was recrystd. from EtOH, dried under vac. (0.4 mmHg); elem. anal.; | 48% |
cyanate
Conditions | Yield |
---|---|
In tetrahydrofuran NaOCN or KOCN was added to a THF soln. of Nb-compound in 2:1 ratio under anhyd. conditions, mixt. was stirred and refluxed for ca. 12 h at 65-70°C; filtered, ppt. was washed with THF, filtrate and washings were evapd. in vacuo (2 h), residue was recrystd. from EtOH, dried under vac. (0.4 mmHg); elem. anal.; | 45% |
pyridine
cyanate
manganese (II) acetate tetrahydrate
trimethyleneglycol
Conditions | Yield |
---|---|
In pyridine; acetonitrile Mn acetate, propanediol and OCN(1-) reacted in MeCN-pyridine; | 32% |
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