Conditions | Yield |
---|---|
addition of Ag2SO4 to liquid HCN;; | 100% |
In neat (no solvent) byproducts: H2SO4; shaking in a closed tube for several hours;; | |
In neat (no solvent) byproducts: H2SO4; shaking in a closed tube for several hours;; |
Conditions | Yield |
---|---|
addition of AgNCO to liquid HCN at 25°C;; | 42% |
ammonium cyanide
silver(I) cyanide
Conditions | Yield |
---|---|
With sodium carbonate; silver nitrate | |
With potassium carbonate; silver nitrate | |
With silver nitrate |
silver(I) cyanide
Conditions | Yield |
---|---|
at 0℃; Sehr zersetzlich; |
silver(I) cyanide
Conditions | Yield |
---|---|
at 25℃; |
A
methyl isocyanate
B
silver(I) cyanide
C
acetonitrile
D
trimethylamine
Conditions | Yield |
---|---|
bei der Destillation; |
Conditions | Yield |
---|---|
at 15℃; higher-boiling form of 3-chloro-2-hydroxy-2-methyl-butyronitrile; | |
at 15℃; lower-boiling form of 3-chloro-2-hydroxy-2-methyl-butyronitrile; |
diethyl ether
cyanogen iodide
A
silver cyanate
B
silver(I) cyanide
1-cyanoformamide
water
A
silver(I) cyanide
B
methylammonium carbonate
Conditions | Yield |
---|---|
With water |
difluorochloromethaneselenenyl chloride
silver(I) cyanide
difluorochloromethyl selenocyanate
Conditions | Yield |
---|---|
in a sealed tube, warming from -78 to 20°C; | 100% |
Dichlor(pentamethyl-2,4-cyclopentadien-1-yl)phosphan
silver(I) cyanide
Dicyan(pentamethyl-2,4-cyclopentadien-1-yl)phosphan
Conditions | Yield |
---|---|
In benzene for 20h; Heating; | 95% |
Conditions | Yield |
---|---|
In acetonitrile; benzene at 90℃; for 2.5h; | 93% |
silver(I) cyanide
bis(perfluoro-n-propyl)-ditelluride
Conditions | Yield |
---|---|
at 22℃; Substitution; | 92% |
Conditions | Yield |
---|---|
In acetonitrile; benzene at 95℃; for 2.75h; | 92% |
In acetonitrile; benzene at 90℃; for 5h; |
silver(I) cyanide
bis(perfluoro-n-butyl)-ditelluride
Conditions | Yield |
---|---|
at 22℃; Substitution; | 89% |
silver(I) cyanide
5-chlorodibenzosuberane
10,11-dihydro-5H-dibenzo[a,d]cycloheptene-5-carbonitrile
Conditions | Yield |
---|---|
In acetonitrile; benzene at 20℃; for 2h; Heating / reflux; | 87% |
In benzene | |
In acetonitrile at 80℃; for 1.5h; |
fluorodichloromethaneselenenyl chloride
silver(I) cyanide
fluorodichloromethyl selenocyanate
Conditions | Yield |
---|---|
shaking, 20°C, 15 min.; | 84.7% |
6-methoxyquinoline N-oxide
silver(I) cyanide
2-cyano-6-methoxyquinoline
Conditions | Yield |
---|---|
With benzoyl chloride In chloroform at 20℃; for 18h; Heating / reflux; | 82% |
silver(I) cyanide
bis(perfluoroisopropyl)-ditelluride
Conditions | Yield |
---|---|
at 22℃; Substitution; | 81% |
silver(I) cyanide
1-cyanophosphirane
Conditions | Yield |
---|---|
In various solvent(s) | 80% |
Conditions | Yield |
---|---|
In neat (no solvent) at 350℃; | 75% |
at 330 - 380℃; Destillation im Vakuum; | |
In melt melting in vacuum at 325°C;; |
Conditions | Yield |
---|---|
In chloroform for 6h; | 75% |
silver(I) cyanide
1,3-diisopropoxy-1,3-dimethyl-1,3-disilacyclobutane
Conditions | Yield |
---|---|
In toluene Heating; | 74% |
silver(I) cyanide
1-Br-2-(t)Bu-1,2-dihydro[1,3,2]diazaborolo[1,5-a]pyridine
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 0.5h; | 73% |
silver(I) cyanide
Tris(trimethylsilyl)methantellurenyl-iodid
Tris(trimethylsilyl)methantellurenyl-cyanid
Conditions | Yield |
---|---|
In benzene for 3h; Ambient temperature; | 72% |
silver(I) cyanide
4-bromo-9,10-dihydro-4H-benzo<4,5>cyclohepta<1,2-b>thiophene
4-cyano-9,10-dihydro-4H-benzo<4,5>cyclohepta<1,2-b>thiophene
Conditions | Yield |
---|---|
In benzene for 12h; Heating; | 70% |
silver(I) cyanide
7-bromo-2,3:5,6-dibenzo-7-azabicyclo<2.2.1>hepta-2,5-diene
2,3:5,6-dibenzo-7-cyano-7-azabicyclo[2.2.1]hepta-2,5-diene
Conditions | Yield |
---|---|
In acetonitrile at 60℃; for 12h; | 70% |
N,N,N,N,N,N-hexamethylphosphoric triamide
7,7-bis(trifluoromethylsulfonyloxy)norbornane
silver(I) cyanide
Conditions | Yield |
---|---|
at 100℃; for 15h; | 69% |
Conditions | Yield |
---|---|
68% |
Conditions | Yield |
---|---|
at 20℃; for 24h; | 65% |
In dichloromethane |
silver(I) cyanide
3-chloro-3,4-dihydro-2,4-diphenyl-2H-1,2,4,3-triazaborole
3-cyano-3,4-dihydro-2,4-diphenyl-2H-1,2,4,3-triazaborole
Conditions | Yield |
---|---|
In acetonitrile at 20℃; Substitution; | 63% |
silver(I) cyanide
phosphorus trichloride
phosphorus tricyanide
Conditions | Yield |
---|---|
In neat (no solvent) heating powdered AgCN in tube to 160°C and passing N2, charged with gaseous PCl3, over it;; | 60% |
In neat (no solvent) heating powdered AgCN in tube to 160°C and passing N2, charged with gaseous PCl3, over it;; | 60% |
In diethyl ether heating in a sealed tube; react. decelerated by addn. of ethyl ether;; |
dimethyl tellurium diiodide
silver(I) cyanide
dimethyltellurium dicyanide
Conditions | Yield |
---|---|
In chloroform for 2h; Ambient temperature; | 59.5% |
silver(I) cyanide
dicyclohexyltellurium diiodide
Conditions | Yield |
---|---|
In acetone for 10h; Ambient temperature; | 58% |
silver(I) cyanide
1-bromo-2,3,4-tri-O-acetyl-α-D-glucuronic acid methyl ester
methyl 3,4-di-O-acetyl-1,2-O-<1-(exo-cyano)ethylidene>-α-D-glucopyranuronate
Conditions | Yield |
---|---|
In xylene Heating; | 58% |
silver(I) cyanide
(S)-Me3CN(a)CHCHN(b)[CH(Ph)Me]BBr(N(a)-B)
A
(S)-Me3CN(a)CHCHN(b)[CH(Ph)Me]B-NC(N(a)-B)
Conditions | Yield |
---|---|
In hexane; acetonitrile for 1h; | A n/a B 57% |
silver(I) cyanide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 20℃; for 22h; | 52% |
5-chloro-10,10-dioxo-11-propyl-5,11-dihydrodibenzo<1,2>thiazepine
silver(I) cyanide
Conditions | Yield |
---|---|
In acetonitrile for 2h; Heating; | 46% |
Silver and its compounds, as well as cyanide and its compounds, are on the Community Right-To-Know List. Reported in EPA TSCA Inventory.
DOT Classification: 6.1; Label: Poison
OSHA PEL: TWA 5 mg(CN)/m3
ACGIH TLV: CL 5 mg(CN)/m3 (skin)
DFG MAK: 5 mg/m3
NIOSH REL: (Cyanide) CL 5 mg(CN)/m3/10M
The IUPAC name of Silver cyanide is silver cyanide. With the CAS registry number 506-64-9, it is also named as Kyanid stribrny. The product's categories are Inorganics; Metal and Ceramic Science; Salts; Silver Salts, and the other registry numbers are 12351-98-3; 29829-51-4. Besides, it is white to off-white powder, which should be stored in sealed package in a cool, dry and well ventilated warehouse away from fire and heat source. It forms structurally complex materials upon reaction with other anions. In addition, this chemical is insoluble in water and incompatible with strong acids, ammonia, hydrogen peroxide. It forms an explosive mixture with fluorine, which may decompose in light.
The other characteristics of this product can be summarized as: (1)EINECS: 208-048-6; (2)H-Bond Donor: 0; (3)H-Bond Acceptor: 2; (4)Rotatable Bond Count: 0; (5)Exact Mass: 132.908167; (6)MonoIsotopic Mass: 132.908167; (7)Topological Polar Surface Area: 23.8; (8)Heavy Atom Count: 3; (9)Complexity: 10; (10)Density: 3.95 g/cm3; (11)Melting point: 300 °C.
Preparation of Silver cyanide: you can add the solution of Silver nitrate to the solution of Potassium cyanide or Sodium cyanide to precipitate. And you will obtain this chemical. The reaction equations are as follows:
or
Uses of Silver cyanide: this chemical is used as lining of autoclave which is used in medicine, silver plating and protective coating. It is also used for electrofacing of electrical contact and engine bearings of airplane. Additionally, it is used as plating reagent and additive of precious metal, analytical reagent. Furthermore, it can be used to produce Oxalonitrile.
This reaction will occur at temperature of 350 °C. The yield is 75 %.
When you are using this chemical, please be cautious about it as the following: it is very toxic by inhalation, in contact with skin and if swallowed. It contacts with acid liberates very toxic gas. Please keep container tightly closed. It is danger of cumulative effects and risk of serious damage to the eyes. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. After contact with skin, wash immediately with plenty of soap-suds. What's more, it is toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. This material and its container must be disposed of as hazardous waste. Please do not empty into drains. And you should avoid release to the environment. Refer to special instructions / safety data sheets. Moreover, in case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.).
People can use the following data to convert to the molecule structure.
(1)SMILES: [C-]#N.[Ag+]
(2)InChI: InChI=1/CN.Ag/c1-2;/q-1;+1
(3)InChIKey: LFAGQMCIGQNPJG-UHFFFAOYAM
(4)Std. InChI: InChI=1S/CN.Ag/c1-2;/q-1;+1
(5)Std. InChIKey: LFAGQMCIGQNPJG-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
rat | LD50 | oral | 123mg/kg (123mg/kg) | "Sbornik Vysledku Toxixologickeho Vysetreni Latek A Pripravku," Marhold, J.V., Institut Pro Vychovu Vedoucicn Pracovniku Chemickeho Prumyclu Praha, Czechoslovakia, 1972Vol. -, Pg. 13, 1972. |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View