CAS 20781-20-8|2,4-Dimethoxybenzylamine
| Common Name | 2,4-Dimethoxybenzylamine | ||
|---|---|---|---|
| CAS Number | 20781-20-8 | Molecular Weight | 167.205 |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 272.4±25.0 °C at 760 mmHg |
| Molecular Formula | C9H13NO2 | Melting Point | / |
| MSDS | ChineseUSA | Flash Point | 128.4±30.4 °C |
| Symbol | GHS05 | Signal Word | Danger |
Names
| Name | (2,4-dimethoxyphenyl)methanamine |
|---|---|
| Synonym | More Synonyms |
Chemical & Physical Properties
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 272.4±25.0 °C at 760 mmHg |
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.205 |
| Flash Point | 128.4±30.4 °C |
| Exact Mass | 167.094635 |
| PSA | 44.48000 |
| LogP | 0.97 |
| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
| Index of Refraction | 1.523 |
| InChIKey | QOWBXWFYRXSBAS-UHFFFAOYSA-N |
| SMILES | COc1ccc(CN)c(OC)c1 |
Safety Information
| Symbol | GHS05 |
|---|---|
| Signal Word | Danger |
| Hazard Statements | H314 |
| Precautionary Statements | P280-P305 + P351 + P338-P310 |
| Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
| Hazard Codes | C:Corrosive; |
| Risk Phrases | R34 |
| Safety Phrases | S26-S27-S36/37/39-S45 |
| RIDADR | UN 2735 8/PG 3 |
| WGK Germany | 3 |
| RTECS | DP4430000 |
| Packaging Group | III |
| Hazard Class | 8 |
| HS Code | 2922299090 |
Customs
| HS Code | 2922299090 |
|---|---|
| Summary | 2922299090. other amino-naphthols and other amino-phenols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |
Articles7
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| Application of the Ugi reaction for the one-pot synthesis of uracil polyoxin C analogues. J. Org. Chem. 74(13) , 4870-3, (2009) A simple, two-step synthesis of amide derivatives of uracil polyoxin C (UPOC) methyl ester using the Ugi reaction is described. The four components employed in the Ugi reaction are 2',3'-isopropylidin... | |
| Synthesis of N-hydroxythiourea. J. Med. Chem. 19(2) , 336-7, (1976) The synthesis of the title compound (1) was accomplished by the conversion of 2,4-dimethoxybenzylamine (2) into an isothiocyanate (3) using thiocarbonyl diimidazole. Treatment of 3 with hydroxylamine ... |
Synonyms
| 2,4-BIPYRIDINE-6-CARBOXYLIC ACID |
| Benzenemethanamine, 2,5-dimethoxy- |
| (2,4-Dimethoxyphenyl)methanamine |
| 2,4-dimethoxy-benzylamine |
| Benzenemethanamine, 2,4-dimethoxy- |
| 1-(2,5-Dimethoxyphenyl)methanamine |
| 1-(2,4-Dimethoxyphenyl)methanamine |
| MFCD00052811 |
| 2,4-dimethoxybenzylamine |
| 2,4-DIMETHOXYBENZYL AMINE |
