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L-Tryptophan,N-[[(6-deoxy-a-L-mannopyranosyl)oxy]hydroxyphosphinyl]-L-leucyl-,sodium salt (9CI) (119942-99-3)

Identification
Name:L-Tryptophan,N-[[(6-deoxy-a-L-mannopyranosyl)oxy]hydroxyphosphinyl]-L-leucyl-,sodium salt (9CI)
Synonyms:L-Tryptophan,N-[N-[[(6-deoxy-a-L-mannopyranosyl)oxy]hydroxyphosphinyl]-L-leucyl]-,sodium salt;NSC 694280;
CAS:119942-99-3
EINECS: 252-996-3
Molecular Formula: C23H32N3Na2O10P
Molecular Weight: 566.493691
InChI: InChI=1S/C23H34N3O10P.Na/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15;/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34);
Molecular Structure: (C23H32N3Na2O10P) L-Tryptophan,N-[N-[[(6-deoxy-a-L-mannopyranosyl)oxy]hydroxyphosphinyl]-L-leucyl]-,sodium salt;NSC 69...
Properties
Flash Point: °C
Boiling Point: °Cat760mmHg
Density:g/cm3
Specification:

The Phosphoramidon disodium salt with cas registry number of 119942-99-3, belongs to the following product categories: (1)Chiral Reagents; (2)Inhibitors; (3)Intermediates & Fine Chemicals; (4)Pharmaceuticals; (5)Phosphorylating and Phosphitylating Agents. And its systematic name is disodium (2S)-3-(1H-indol-3-yl)-2-({(2S)-4-methyl-2-[({[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}phosphinato)amino]pentanoyl}amino)propanoate (non-preferred name).

Physical properties about this chemical are: (1)#H bond acceptors: 13; (2)#H bond donors: 8; (3)#Freely Rotating Bonds: 13; (4)Polar Surface Area: 164.7 Å2. Its storage temperature is −20°C. Its main usage is an endothelin-converting enzyme inhibitor, attenuates lipopolysaccharide-induced acute lung injury.

When you are using this chemical, please be cautious about it as the following:
Do not breathe dust and avoid contact with skin and eyes.

You can still convert the following datas into molecular structure: 
(1)SMILES:[Na+].[Na+].O=P([O-])(O[C@@H]1O[C@H]([C@H](O)[C@@H](O)[C@H]1O)C)N[C@H](C(=O)N[C@H](C([O-])=O)Cc3c2ccccc2nc3)CC(C)C;
(2)InChI:InChI=1/C23H34N3O10P.2Na/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15;;/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34);;/q;2*+1/p-2/t12-,16-,17-,18-,19+,20+,23-;;/m0../s1;
(3)InChIKey:OQKHVXFOYFBMDJ-XUGQDIOPBT;
(4)Std. InChI:InChI=1S/C23H34N3O10P.2Na/c1-11(2)8-16(26-37(33,34)36-23-20(29)19(28)18(27)12(3)35-23)21(30)25-17(22(31)32)9-13-10-24-15-7-5-4-6-14(13)15;;/h4-7,10-12,16-20,23-24,27-29H,8-9H2,1-3H3,(H,25,30)(H,31,32)(H2,26,33,34);;/q;2*+1/p-2/t12-,16-,17-,18-,19+,20+,23-;;/m0../s1;
(5)Std. InChIKey:OQKHVXFOYFBMDJ-ODIUWQMJSA-L

Flash Point: °C
Storage Temperature: −20°C
Usage:An endothelin-converting enzyme inhibitor, attenuates lipopolysaccharide-induced acute lung injury.
Safety Data
 

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