- Product Details
Keywords
- NSC 607750
- Thiodiacetonitrile
- Thiobisacetonitrile
Quick Details
- ProName: Acetonitrile,2,2'-thiobis-
- CasNo: 5848-75-9
- Application: The Acetonitrile,2,2'-thiobis- is an o...
- ProductionCapacity: Metric Ton/Day
- Purity: 99
- Transportation: The Acetonitrile,2,2'-thiobis- is an o...
- LimitNum: 0 Metric Ton
Superiority
The Acetonitrile,2,2'-thiobis- is an organic compound with the formula C4H4N2S. The systematic name of this chemical is 2,2'-sulfanediyldiacetonitrile. With the CAS registry number 5848-75-9, it is also named as 2-[(cyanomethyl)thio]acetonitrile.
Physical properties about Acetonitrile,2,2'-thiobis- are: (1)ACD/LogP: -0.09; (2)#H bond acceptors: 2; (3)#Freely Rotating Bonds: 2; (4)Polar Surface Area: 72.88 Å2; (5)Index of Refraction: 1.507; (6)Molar Refractivity: 28.4 cm3; (7)Molar Volume: 95.2 cm3; (8)Polarizability: 11.26×10-24cm3; (9)Surface Tension: 54.1 dyne/cm; (10)Density: 1.176 g/cm3; (11)Flash Point: 123.2 °C; (12)Enthalpy of Vaporization: 51.89 kJ/mol; (13)Boiling Point: 280.2 °C at 760 mmHg; (14)Vapour Pressure: 0.00384 mmHg at 25°C.
Preparation of Acetonitrile,2,2'-thiobis-: this chemical can be prepared by chloroacetonitrile. This reaction will need reagents diethyl ether, NH3, H2S.
Uses of Acetonitrile,2,2'-thiobis-: it can be used to produce 1H,1'H-5,5'-sulfanediyldimethyl-bis-tetrazole by heating. It will need reagents NaN3, NH4Cl, LiF and solvent dimethylformamide with reaction time of 40 hours. The yield is about 71.5%.
You can still convert the following datas into molecular structure:
(1)SMILES: N#CCSCC#N
(2)InChI: InChI=1/C4H4N2S/c5-1-3-7-4-2-6/h3-4H2
(3)InChIKey: YFUCPLPDBPZLGK-UHFFFAOYAW
(4)Std. InChI: InChI=1S/C4H4N2S/c5-1-3-7-4-2-6/h3-4H2
(5)Std. InChIKey: YFUCPLPDBPZLGK-UHFFFAOYSA-N
Details
The Acetonitrile,2,2'-thiobis- is an organic compound with the formula C4H4N2S. The systematic name of this chemical is 2,2'-sulfanediyldiacetonitrile. With the CAS registry number 5848-75-9, it is also named as 2-[(cyanomethyl)thio]acetonitrile.
Physical properties about Acetonitrile,2,2'-thiobis- are: (1)ACD/LogP: -0.09; (2)#H bond acceptors: 2; (3)#Freely Rotating Bonds: 2; (4)Polar Surface Area: 72.88 Å2; (5)Index of Refraction: 1.507; (6)Molar Refractivity: 28.4 cm3; (7)Molar Volume: 95.2 cm3; (8)Polarizability: 11.26×10-24cm3; (9)Surface Tension: 54.1 dyne/cm; (10)Density: 1.176 g/cm3; (11)Flash Point: 123.2 °C; (12)Enthalpy of Vaporization: 51.89 kJ/mol; (13)Boiling Point: 280.2 °C at 760 mmHg; (14)Vapour Pressure: 0.00384 mmHg at 25°C.
Preparation of Acetonitrile,2,2'-thiobis-: this chemical can be prepared by chloroacetonitrile. This reaction will need reagents diethyl ether, NH3, H2S.
Uses of Acetonitrile,2,2'-thiobis-: it can be used to produce 1H,1'H-5,5'-sulfanediyldimethyl-bis-tetrazole by heating. It will need reagents NaN3, NH4Cl, LiF and solvent dimethylformamide with reaction time of 40 hours. The yield is about 71.5%.
You can still convert the following datas into molecular structure:
(1)SMILES: N#CCSCC#N
(2)InChI: InChI=1/C4H4N2S/c5-1-3-7-4-2-6/h3-4H2
(3)InChIKey: YFUCPLPDBPZLGK-UHFFFAOYAW
(4)Std. InChI: InChI=1S/C4H4N2S/c5-1-3-7-4-2-6/h3-4H2
(5)Std. InChIKey: YFUCPLPDBPZLGK-UHFFFAOYSA-N