Product Name

  • Name

    Cesium formate

  • EINECS 222-492-8
  • CAS No. 3495-36-1
  • Article Data25
  • CAS DataBase
  • Density 1.017 [CRC10]
  • Solubility very soluble H2O [CRC10]
  • Melting Point 50 °C
  • Formula CHCsO2
  • Boiling Point 100.6oC at 760mmHg
  • Molecular Weight 177.923
  • Flash Point 29.9oC
  • Transport Information
  • Appearance granular solid
  • Safety 22-24/25-36/37/39-26
  • Risk Codes 36/37/38
  • Molecular Structure Molecular Structure of 3495-36-1 (Cesium formate)
  • Hazard Symbols IrritantXi
  • Synonyms Cesiumformate (7CI);Formic acid, cesium salt (8CI,9CI);
  • PSA 40.13000
  • LogP -0.99800

Synthetic route

methanol
67-56-1

methanol

carbon dioxide
124-38-9

carbon dioxide

carbon monoxide
201230-82-2

carbon monoxide

caesium carbonate
534-17-8

caesium carbonate

A

Dimethyl oxalate
553-90-2

Dimethyl oxalate

B

cesium bicarbonate
15519-28-5

cesium bicarbonate

C

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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%
formic acid
64-18-6

formic acid

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
With cesium hydroxide In water80%
methanol
67-56-1

methanol

carbon dioxide
124-38-9

carbon dioxide

caesium carbonate
534-17-8

caesium carbonate

A

Dimethyl oxalate
553-90-2

Dimethyl oxalate

B

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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
124-38-9

carbon dioxide

caesium carbonate
534-17-8

caesium carbonate

A

cesium bicarbonate
15519-28-5

cesium bicarbonate

B

cesium oxalate
1068-63-9

cesium oxalate

C

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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
124-38-9

carbon dioxide

carbon monoxide
201230-82-2

carbon monoxide

caesium carbonate
534-17-8

caesium carbonate

A

cesium bicarbonate
15519-28-5

cesium bicarbonate

B

cesium oxalate
1068-63-9

cesium oxalate

C

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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
201230-82-2

carbon monoxide

caesium carbonate
534-17-8

caesium carbonate

A

cesium bicarbonate
15519-28-5

cesium bicarbonate

B

cesium oxalate
1068-63-9

cesium oxalate

C

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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%
C12H11N2O6(1-)*Cs(1+)

C12H11N2O6(1-)*Cs(1+)

A

carbon dioxide
124-38-9

carbon dioxide

B

cesium formate
3495-36-1

cesium formate

C

Caesium; 2,4-dinitro-naphthalen-1-olate

Caesium; 2,4-dinitro-naphthalen-1-olate

Conditions
ConditionsYield
at 141 - 164℃; Product distribution; Thermodynamic data; ΔH of the decomposition;
formic acid
64-18-6

formic acid

caesium carbonate
534-17-8

caesium carbonate

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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;;
caesium hydride

caesium hydride

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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;
caesium hydride

caesium hydride

carbon dioxide
124-38-9

carbon dioxide

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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;;
caesium hexa(formato)ferrate(III)

caesium hexa(formato)ferrate(III)

A

formyloxy radical
16499-21-1

formyloxy radical

B

iron(II)
7439-89-6

iron(II)

C

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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.;
Cs(1+)*HCO2(1-)*99H2O=CsHCO2*99H2O

Cs(1+)*HCO2(1-)*99H2O=CsHCO2*99H2O

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
In not given water was removed from hydrated formiate before examination it thermal decomposition; detd. by XRD and IR;
caesium formate*1.5hydrogen peroxide

caesium formate*1.5hydrogen peroxide

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
byproducts: caesium oxalate; exothermally decompn. at 38-55°C;
methanol
67-56-1

methanol

cesium bicarbonate
15519-28-5

cesium bicarbonate

A

caesium methyl carbonate
41792-71-6

caesium methyl carbonate

B

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
With tris(triphenylphosphine)ruthenium(II) chloride; hydrogen at 110℃; under 15201 Torr; for 16h; Catalytic behavior; Inert atmosphere;
cesium bicarbonate
15519-28-5

cesium bicarbonate

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
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
124-38-9

carbon dioxide

caesium isobutyrate

caesium isobutyrate

benzene
71-43-2

benzene

A

caesium malonate

caesium malonate

B

caesium methane tricarboxylate

caesium methane tricarboxylate

C

cesium acetate
3396-11-0

cesium acetate

D

cesium benzoate
17265-04-2

cesium benzoate

E

cesium formate
3495-36-1

cesium formate

G

caesium isophthalate
17839-45-1, 22208-45-3

caesium isophthalate

H

dicaesium terephthalate

dicaesium terephthalate

Conditions
ConditionsYield
With caesium carbonate at 360℃; for 8h; Sealed tube; Overall yield = 19 %Spectr.;
carbon dioxide
124-38-9

carbon dioxide

caesium carbonate
534-17-8

caesium carbonate

A

cesium oxalate
1068-63-9

cesium oxalate

B

cesium formate
3495-36-1

cesium formate

Conditions
ConditionsYield
With hydrogen at 325℃; under 750.075 Torr;
10CH4O*4Nb(2+)*14Cl(1-)*2Nb(3+)

10CH4O*4Nb(2+)*14Cl(1-)*2Nb(3+)

cesium formate
3495-36-1

cesium formate

[Cs(methanol)]4[Nb6Cl12(formate)6]

[Cs(methanol)]4[Nb6Cl12(formate)6]

Conditions
ConditionsYield
In methanol for 10h;95%
tetra-n-butylphosphonium tetrafluoroborate

tetra-n-butylphosphonium tetrafluoroborate

cesium formate
3495-36-1

cesium formate

tetra-n-butylphosphonium formate
78251-52-2

tetra-n-butylphosphonium formate

Conditions
ConditionsYield
In ethanol90%
[Ni(bis-1,2-dimethylphosphinobenzene)2][BF4]2

[Ni(bis-1,2-dimethylphosphinobenzene)2][BF4]2

cesium formate
3495-36-1

cesium formate

[Ni(bis-1,2-dimethylphosphinobenzene)2H][BF4]

[Ni(bis-1,2-dimethylphosphinobenzene)2H][BF4]

Conditions
ConditionsYield
In acetonitrile Inert atmosphere;85%
1-methyl-1-propylpyrrolidinium hexafluorophosphate

1-methyl-1-propylpyrrolidinium hexafluorophosphate

cesium formate
3495-36-1

cesium formate

C8H18N(1+)*CHO2(1-)

C8H18N(1+)*CHO2(1-)

Conditions
ConditionsYield
In isopropyl alcohol at 20℃; for 48h;77%
tetraoctylphosphonium tetrafluoroborate

tetraoctylphosphonium tetrafluoroborate

cesium formate
3495-36-1

cesium formate

tetra-n-octylphosphonium formate

tetra-n-octylphosphonium formate

Conditions
ConditionsYield
In isopropyl alcohol at 20℃;76%
In isopropyl alcohol for 16h;
trimethylsilylazide
4648-54-8

trimethylsilylazide

2-phenylethyl acrylate
3530-36-7

2-phenylethyl acrylate

cesium formate
3495-36-1

cesium formate

C13H16O4

C13H16O4

Conditions
ConditionsYield
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
3495-36-1

cesium formate

(+)-(1S,3S)-(2,2-dimethyl-6-methylene-3-p-toluenesulfonyloxycyclohexyl)methyl p-toluenesulfonate
105996-72-3

(+)-(1S,3S)-(2,2-dimethyl-6-methylene-3-p-toluenesulfonyloxycyclohexyl)methyl p-toluenesulfonate

(1S,3S)-(+)-2,2-dimethyl-6-methylene-3-tosyloxycyclohexanemethyl formate
105996-73-4

(1S,3S)-(+)-2,2-dimethyl-6-methylene-3-tosyloxycyclohexanemethyl formate

Conditions
ConditionsYield
With perhydrodibenzo-18-crown-6 In methanol; toluene at 110℃; for 35h;66.6%
cesium formate
3495-36-1

cesium formate

3-epi-3-trifluoromethanesulfonyl-altholactone
162630-71-9

3-epi-3-trifluoromethanesulfonyl-altholactone

3-formyloxy-altholactone
359435-67-9

3-formyloxy-altholactone

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 4h;60%
trimethylsilylazide
4648-54-8

trimethylsilylazide

cesium formate
3495-36-1

cesium formate

methyl α-(phenylsulfonyl)propionate
85979-85-7

methyl α-(phenylsulfonyl)propionate

Conditions
ConditionsYield
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%
ethyl crotonate
10544-63-5

ethyl crotonate

benzyl bromide
100-39-0

benzyl bromide

cesium formate
3495-36-1

cesium formate

benzyl ethyl 2-ethylmalonate

benzyl ethyl 2-ethylmalonate

Conditions
ConditionsYield
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
100-39-0

benzyl bromide

cesium formate
3495-36-1

cesium formate

methyl methacrylate
97-63-2

methyl methacrylate

1-benzyl 3-ethyl 2,2-dimethylmalonate
1347024-62-7

1-benzyl 3-ethyl 2,2-dimethylmalonate

Conditions
ConditionsYield
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
3381-51-9

(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
3495-36-1

cesium formate

A

5α-cholest-3-ene
28338-69-4

5α-cholest-3-ene

C

3α-cholestanyl formate
42921-34-6

3α-cholestanyl formate

Conditions
ConditionsYield
With dmap In toluene for 96h; Heating;A n/a
B n/a
C 13%
cesium formate
3495-36-1

cesium formate

caesium carbonate
534-17-8

caesium carbonate

Conditions
ConditionsYield
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
3495-36-1

cesium formate

A

methane
34557-54-5

methane

B

carbon dioxide
124-38-9

carbon dioxide

C

carbon monoxide
201230-82-2

carbon monoxide

D

cesium oxalate
1068-63-9

cesium oxalate

E

caesium carbonate
534-17-8

caesium carbonate

Conditions
ConditionsYield
In solid byproducts: C, CH3OH, HCO2CH3; thermal decomposition of CsHCO2 under N2 at 200-250°C; detd. by XRD and IR;
cesium formate
3495-36-1

cesium formate

cesium triformato-stannate(II)

cesium triformato-stannate(II)

Cesium formate Specification

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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