Raphanusamic acid
Raphanusamic acid structure
|
Common Name | Raphanusamic acid | ||
|---|---|---|---|---|
| CAS Number | 98169-56-3 | Molecular Weight | 163.21800 | |
| Density | 1.65g/cm3 | Boiling Point | 359.4ºC at 760mmHg | |
| Molecular Formula | C4H5NO2S2 | Melting Point | 179-181ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 171.1ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
A glucosinolate metabolism pathway in living plant cells mediates broad-spectrum antifungal defense.
Science 323(5910) , 101-6, (2009) Selection pressure exerted by insects and microorganisms shapes the diversity of plant secondary metabolites. We identified a metabolic pathway for glucosinolates, known insect deterrents, that differs from the pathway activated by chewing insects. This pathw... |
|
|
Identification of a new urinary metabolite of carbon disulfide using an improved method for the determination of 2-thioxothiazolidine-4-carboxylic acid.
Chem. Res. Toxicol. 14(9) , 1277-83, (2001) A new method is reported for the analysis of 2-thioxothiazolidine-4-carboxylic acid (TTCA) in urine that is amenable to automation and provides greatly simplified chromatograms. The method comprises the addition of tetrahydro-2-thioxo-2H-1,3-thiazine-4-carbox... |
|
|
Chloropicrin dechlorination in relation to toxic action.
J. Biochem. Mol. Toxicol. 14(1) , 26-32, (2000) Chloropicrin (CCl3NO2) is a widely used soil fumigant with an unknown mechanism of acute toxicity. We investigated the possible involvement of dechlorination in CCl3NO2 toxicity by considering its metabolism, inhibition of pyruvate and succinate dehydrogenase... |
|
|
(4R)-(-)-2-thioxothiazolidine-4-carboxylic acid (raphanusamic acid).
Acta Crystallogr. C 54 ( Pt 11) , 1634-7, (1998) The title acid, C4H5NO2S2, crystallized in the noncentrosymmetric space group P2(1)2(1)2(1) with one molecule as the asymmetric unit. Two hydrogen bonds occur, namely, N--H...O, with a donor-acceptor distance of 2.850 (2) A, and O-H...S (resonance induced), w... |