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Name |
Phosphoramidous acid, N, N-bis(1-methylethyl)-, bis(2-cyanoethyl) ester |
EINECS | 802-449-5 |
CAS No. | 102690-88-0 | Density | 1.039 g/mL at 25 °C |
PSA | 82.87000 | LogP | 3.19266 |
Solubility | N/A | Melting Point |
N/A |
Formula | C12H22N3O2P | Boiling Point | 335.3 °C at 760 mmHg |
Molecular Weight | 271.299 | Flash Point | 156.6 °C |
Transport Information | N/A | Appearance | N/A |
Safety | 26-36-37-39-45 | Risk Codes |
Xi:Irritant; |
Molecular Structure | Hazard Symbols | Xi | |
Synonyms |
Phosphoramidousacid, bis(1-methylethyl)-, bis(2-cyanoethyl) ester (9CI);Bis(2-cyanoethoxy)(diisopropylamino)phosphine;Bis(2-cyanoethoxy)-N, N-diisopropylaminophosphine; |
Article Data | 14 |
The Phosphoramidous acid, N, N-bis(1-methylethyl)-, bis(2-cyanoethyl) ester, with the CAS registry number 102690-88-0, is also known as Bis(2-cyanoethoxy)-N, N-diisopropylaminophosphine. It belongs to the product categories of Phospholipids - 13C & 2H; Phosphorylating and Phosphitylating Agents. This chemical's molecular formula is C12H22N3O2P and molecular weight is 271.3. What's more, its systematic name is Bis(2-cyanoethyl) bis(1-methylethyl)amidophosphite. In addition, this chemical may cause inflammation to the skin or other mucous membranes.
Physical properties about Phosphoramidous acid, N, N-bis(1-methylethyl)-, bis(2-cyanoethyl) ester are: (1)ACD/LogP: 2.55; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 2.55; (4)ACD/LogD (pH 7.4): 2.55; (5)ACD/BCF (pH 5.5): 50.97; (6)ACD/BCF (pH 7.4): 51.17; (7)ACD/KOC (pH 5.5): 579.68; (8)ACD/KOC (pH 7.4): 582.03; (9)#H bond acceptors: 5; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 9; (12)Polar Surface Area: 82.87 Å2; (13)Flash Point: 156.6 °C; (14)Enthalpy of Vaporization: 57.84 kJ/mol; (15)Boiling Point: 335.3 °C at 760 mmHg; (16)Vapour Pressure: 0.000121 mmHg at 25 °C.
Preparation of Phosphoramidous acid, N, N-bis(1-methylethyl)-, bis(2-cyanoethyl) ester: this chemical is prepared by reaction of 3-Hydroxy-propionitrile with 2-Cyanoethyl-bis(N, N-diisopropyl)amino phosphite at ambient temperature. The reaction needs reagent Tetrazole and solvent CH2Cl2. Besides, the reaction time is 1 hour.
Uses of Phosphoramidous acid, N, N-bis(1-methylethyl)-, bis(2-cyanoethyl) ester: it is used to produce other chemicals. For example, it is used to produce Bis(2-cyanoethyl) 2, 4-di-O-acetyl-3, 6-dideoxy-3-C-methylene-β-D-ribo-hexopyranosyl phosphate at ambient temperature. This reaction needs reagent 1H-Tetrazole. Meanwhile, it needs solvents CH2Cl2 and Acetonitrile. The reaction time is 20 minutes and the yield is about 86 %.
You can still convert the following datas into molecular structure:
(1) SMILES: N#CCCOP(OCCC#N)N(C(C)C)C(C)C
(2) InChI: InChI=1/C12H22N3O2P/c1-11(2)15(12(3)4)18(16-9-5-7-13)17-10-6-8-14/h11-12H,5-6,9-10H2,1-4H3
(3) InChIKey: LDHWBEHZLFDXCU-UHFFFAOYAH