CAS 95-43-2|D-(-)-threose
Introduction：Basic information about CAS 95-43-2|D-(-)-threose, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | D-(-)-threose | ||
|---|---|---|---|
| CAS Number | 95-43-2 | Molecular Weight | 120.10400 |
| Density | 1.41g/cm3 | Boiling Point | 311.1ºC at 760mmHg |
| Molecular Formula | C4H8O4 | Melting Point | 130℃ |
| MSDS | USA | Flash Point | 156.2ºC |
Names
| Name | D-threose |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.41g/cm3 |
|---|---|
| Boiling Point | 311.1ºC at 760mmHg |
| Melting Point | 130℃ |
| Molecular Formula | C4H8O4 |
| Molecular Weight | 120.10400 |
| Flash Point | 156.2ºC |
| Exact Mass | 120.04200 |
| PSA | 69.92000 |
| Index of Refraction | 1.619 |
| InChIKey | YTBSYETUWUMLBZ-QWWZWVQMSA-N |
| SMILES | O=CC(O)C(O)CO |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2912491000 |
Customs
| HS Code | 2912491000 |
|---|---|
| Summary | 2912491000. other aldehyde-alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Articles25
More Articles| The silicate-mediated formose reaction: bottom-up synthesis of sugar silicates. Science 327(5968) , 984-6, (2010) Understanding the mechanism of sugar formation and stabilization is important for constraining theories on the abiotic origin of complex biomolecules. Although previous studies have produced sugars fr... | |
| Formation of furan and methylfuran from ascorbic acid in model systems and food. Food Addit. Contam. 24 Suppl 1 , 122-35, (2007) Previous model studies have suggested ascorbic acid as one of the major sources of furan, a possibly hazardous compound found in thermally processed foods (e.g. canned products, jars). The study showe... | |
| Nonenzymatic oligomerization of RNA by TNA templates. Org. Lett. 8(25) , 5809-11, (2006) Cytosine TNA promotes nonenzymatic, template-directed oligomerization of complementary activated rGMP, leading to selective and efficient formation of RNA products. This process models "genetic takeov... |
Synonyms
| (S-(R*,S*))-2,3,4-trihydroxy-butanal |
| N-(tert-Butoxycarbonyl)-D-2-phenylglycine |
| BENZENESULFONAMIDE, 4-CHLORO-N-(1-CYCLOHEXYL-1H-IMIDAZOL-2-YL)- |
| N-Boc-D-phenylglycine |
| (1R,2R)-2-Amino-1-(4-methylmercapto-phenyl)-propan-1,3-diol |
| MFCD00043042 |
| (S(R*,R*))-2-amino-1-[p-(methylthio)phenyl]propane-1,3-diol |
| (-)-(1R,2R)-2-Amino-1-<4-(methylthio)phenyl>-1,3-propanediol |
| (1R,2R)-2-amino-1-(4-methylsulfanyl-phenyl)-propane-1,3-diol |
| Boc-D-Phg-OH |
| D-(-)-threose |
| (2S,3R)-2,3,4-Trihydroxybutanal |
| Dg-threo-2,3,4-Trihydroxy-butyraldehyd |
| N-Boc-L-phenylglycine |
| Boc-(R)-phenylglycine |
| EINECS 202-418-0 |
| Boc-D-Phenylglycine |
| (R)-Boc-phenylglycine |
| D-N-Boc-phenylglycine |
| (R*,R*)-(+)-thiomicamine |
| (R)-2-[(tert-butoxy)carbonylamino]-2-phenylacetic acid |
| D-(-)-threo-2-amino-1-(4-(methylthio)phenyl)-1,3-propanediol |
| (R(R*,R*))-2-amino-1-[p-(methylthio)phenyl]propane-1,3-diol |
| (2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acid |
