methanol
carbon dioxide
carbon monoxide
caesium carbonate
A
Dimethyl oxalate
B
cesium bicarbonate
C
cesium formate
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; carbon monoxide; caesium carbonate With silica gel; pyrographite at 325℃; under 15001.5 - 33753.4 Torr; Stage #2: methanol at 200℃; under 30003 Torr; for 2h; Reagent/catalyst; Temperature; Pressure; | A 95% B n/a C 0.8% |
Conditions | Yield |
---|---|
With cesium hydroxide In water | 80% |
methanol
carbon dioxide
caesium carbonate
A
Dimethyl oxalate
B
cesium formate
Conditions | Yield |
---|---|
Stage #1: carbon dioxide; caesium carbonate With hydrogen at 325℃; under 750.075 Torr; Stage #2: methanol at 150℃; under 26252.6 Torr; | A 58% B 10% |
carbon dioxide
caesium carbonate
A
cesium bicarbonate
B
cesium oxalate
C
cesium formate
Conditions | Yield |
---|---|
In neat (no solvent) High Pressure; 2 h at 380°C; cooling, dissolution in water, addn. of HClO4; HPLC; | A 39.2% B 0% C 0% |
carbon dioxide
carbon monoxide
caesium carbonate
A
cesium bicarbonate
B
cesium oxalate
C
cesium formate
Conditions | Yield |
---|---|
In neat (no solvent) High Pressure; 2 h at 380°C; cooling, dissolution in water, addn. of HClO4; HPLC; | A 0.1% B 22.4% C 2.1% |
carbon monoxide
caesium carbonate
A
cesium bicarbonate
B
cesium oxalate
C
cesium formate
Conditions | Yield |
---|---|
In neat (no solvent) High Pressure; 2 h at 380°C; cooling, dissolution in water, addn. of HClO4; HPLC; | A 0% B 4.4% C 6.9% |
Conditions | Yield |
---|---|
at 141 - 164℃; Product distribution; Thermodynamic data; ΔH of the decomposition; |
Conditions | Yield |
---|---|
In neat (no solvent) purified Cs2CO3 was neutralized with formic acid forming CsHCO2;; | |
In neat (no solvent) Na-containing Cs2CO3 was treated with formic acid forming CsHCO2;; recrystn. from formic acid, remaining acid was removed with Cs2CO3, recrystn. from alcoholic soln. with addn. of ether;; | |
In neat (no solvent) Na-containing Cs2CO3 was treated with formic acid forming CsHCO2;; recrystn. from formic acid, remaining acid was removed with Cs2CO3, recrystn. from alcoholic soln. with addn. of ether;; |
cesium formate
Conditions | Yield |
---|---|
With carbon dioxide reaction proceeds only in presence of traces of H2O; moist CO2 reacts at -75°C, well dried CO2 at +42°C; | |
With CO2 reaction proceeds only in presence of traces of H2O; moist CO2 reacts at -75°C, well dried CO2 at +42°C; |
Conditions | Yield |
---|---|
With water In neat (no solvent) CsH was treated with CO2 at ambient temp. in presence of traces of water forming CsHCO2; in absence of moisture reaction occured only with heating to 54 °C;; | |
With H2O In neat (no solvent) CsH was treated with CO2 at ambient temp. in presence of traces of water forming CsHCO2; in absence of moisture reaction occured only with heating to 54 °C;; |
Conditions | Yield |
---|---|
In solid Irradiation (UV/VIS); Solid state photolysis is investigated by exposing the complex to 250 W Hg-lamp.; detected by Moessbauer spectroscopy; | A n/a B n/a C 0% |
In sulfuric acid Irradiation (UV/VIS); Alkali hexa(formato)ferrate(III) is subjected to photolysis by irradiating it with radiations from a mercury lamp, 1,10-phenanthroline is added, photochemical reduction is studied at 25°C.; |
cesium formate
Conditions | Yield |
---|---|
In not given water was removed from hydrated formiate before examination it thermal decomposition; detd. by XRD and IR; |
cesium formate
Conditions | Yield |
---|---|
byproducts: caesium oxalate; exothermally decompn. at 38-55°C; |
methanol
cesium bicarbonate
A
caesium methyl carbonate
B
cesium formate
Conditions | Yield |
---|---|
With tris(triphenylphosphine)ruthenium(II) chloride; hydrogen at 110℃; under 15201 Torr; for 16h; Catalytic behavior; Inert atmosphere; |
cesium bicarbonate
cesium formate
Conditions | Yield |
---|---|
With {RuCl2(m-triphenylphosphine trisulfonate)2}2; hydrogen; tris-(m-sulfonatophenyl)phosphine In water at 80℃; under 75007.5 Torr; for 20h; Concentration; Autoclave; | |
With carbonyl chlorohydride{bis[2-(bis-tert-butylphosphino)ethyl]amine}ruthenium(II); hydrogen In 2-methyltetrahydrofuran; water at 80℃; under 37503.8 Torr; for 1.05h; | 98 %Spectr. |
carbon dioxide
benzene
C
cesium acetate
D
cesium benzoate
E
cesium formate
F
cesium o-phthalate
G
caesium isophthalate
Conditions | Yield |
---|---|
With caesium carbonate at 360℃; for 8h; Sealed tube; Overall yield = 19 %Spectr.; |
carbon dioxide
caesium carbonate
A
cesium oxalate
B
cesium formate
Conditions | Yield |
---|---|
With hydrogen at 325℃; under 750.075 Torr; |
Conditions | Yield |
---|---|
In methanol for 10h; | 95% |
cesium formate
tetra-n-butylphosphonium formate
Conditions | Yield |
---|---|
In ethanol | 90% |
cesium formate
Conditions | Yield |
---|---|
In acetonitrile Inert atmosphere; | 85% |
Conditions | Yield |
---|---|
In isopropyl alcohol at 20℃; for 48h; | 77% |
Conditions | Yield |
---|---|
In isopropyl alcohol at 20℃; | 76% |
In isopropyl alcohol for 16h; |
Conditions | Yield |
---|---|
Stage #1: 2-phenylethyl acrylate; cesium formate With carbon dioxide; C38H55F3GeO3P2PdS In 1,4-dioxane at 80℃; under 760.051 Torr; for 6h; Inert atmosphere; Green chemistry; Stage #2: trimethylsilylazide In methanol; diethyl ether at 0℃; for 0.5h; Inert atmosphere; Green chemistry; regioselective reaction; | 75% |
cesium formate
(+)-(1S,3S)-(2,2-dimethyl-6-methylene-3-p-toluenesulfonyloxycyclohexyl)methyl p-toluenesulfonate
(1S,3S)-(+)-2,2-dimethyl-6-methylene-3-tosyloxycyclohexanemethyl formate
Conditions | Yield |
---|---|
With perhydrodibenzo-18-crown-6 In methanol; toluene at 110℃; for 35h; | 66.6% |
cesium formate
3-epi-3-trifluoromethanesulfonyl-altholactone
3-formyloxy-altholactone
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 4h; | 60% |
trimethylsilylazide
PVS
cesium formate
methyl α-(phenylsulfonyl)propionate
Conditions | Yield |
---|---|
Stage #1: PVS; cesium formate With carbon dioxide; C38H55F3GeO3P2PdS In 1,4-dioxane at 80℃; under 760.051 Torr; for 6h; Green chemistry; Stage #2: trimethylsilylazide In methanol; diethyl ether at 0℃; for 0.5h; Green chemistry; regioselective reaction; | 59% |
Conditions | Yield |
---|---|
Stage #1: ethyl crotonate; cesium formate With C22H31F3GeO3P2PdS In N,N-dimethyl-formamide at 80℃; for 6h; Inert atmosphere; Green chemistry; Stage #2: benzyl bromide With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 20℃; for 12h; Green chemistry; regioselective reaction; | 50% |
benzyl bromide
cesium formate
methyl methacrylate
1-benzyl 3-ethyl 2,2-dimethylmalonate
Conditions | Yield |
---|---|
Stage #1: cesium formate; methyl methacrylate With C22H31F3GeO3P2PdS In N,N-dimethyl-formamide at 80℃; for 6h; Inert atmosphere; Green chemistry; Stage #2: benzyl bromide With potassium carbonate; sodium iodide In N,N-dimethyl-formamide at 20℃; for 12h; Inert atmosphere; Green chemistry; regioselective reaction; | 40% |
(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl methanesulfonate
cesium formate
A
5α-cholest-3-ene
B
cholest-2-ene
C
3α-cholestanyl formate
Conditions | Yield |
---|---|
With dmap In toluene for 96h; Heating; | A n/a B n/a C 13% |
Conditions | Yield |
---|---|
In neat (no solvent) Kinetics; heating in air up to 600°C under atmospheric pressure and humidity (heating rate 5-10°C/min); thermogravimetric monitoring; |
cesium formate
A
methane
B
carbon dioxide
C
carbon monoxide
D
cesium oxalate
E
caesium carbonate
Conditions | Yield |
---|---|
In solid byproducts: C, CH3OH, HCO2CH3; thermal decomposition of CsHCO2 under N2 at 200-250°C; detd. by XRD and IR; |
cesium formate
tin(II) formate
The IUPAC name of Cesium formate is Cesium formic acid. With the CAS registry number 3495-36-1, it is also named as Formic acid, cesium salt. The product's category is metallorganics and it is hygroscopic. In addition, it is granular solid, which should be stored in closed, dark, ventilated and dry place at ambient temperature. Its molecular formula is CHCsO2 and molecular weight is 177.92.
The other characteristics of this product can be summarized as: (1)EINECS: 222-492-8; (2)H-Bond Donor: 1; (3)H-Bond Acceptor: 2; (4)Rotatable Bond Count: 0; (5)Exact Mass: 178.910926; (6)MonoIsotopic Mass: 178.910926; (7)Topological Polar Surface Area: 37.3; (8)Heavy Atom Count: 4; (9)Formal Charge: 1; (10)Complexity: 10.3; (11)Melting Point: 50 °C; (12)Boiling Point: 100.6 °C at 760 mmHg; (13)Flash Point: 29.9 °C.
Uses of Cesium formate: it can reacts with 3-Epi-3-trifluoromethanesulfonyl-altholactone to get 3-Formyloxy-altholactone.
This reaction needs Dimethylformamide at temperature of 20 °C. The reaction time is 4 hours. The yield is 60 %.
When you are using this chemical, please be cautious about it as the following: Cesium formate is irritating to eyes, respiratory system and skin.When you use it, please wear suitable protective clothing, gloves and eye/face protection to avoid contact with skin and eyes, and do not breathe dust. Moreover, in case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
People can use the following data to convert to the molecule structure.
SMILES:[Cs]OC=O
InChI:InChI=1/CH2O2.Cs/c2-1-3;/h1H,(H,2,3);/q;+1/p-1/rCHCsO2/c2-4-1-3/h1H
InChIKey:ATZQZZAXOPPAAQ-SQJYZGIVAT
Std. InChI:InChI=1S/CH2O2.Cs/c2-1-3;/h1H,(H,2,3);/q;+1/p-1
Std. InChIKey:ATZQZZAXOPPAAQ-UHFFFAOYSA-M
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