There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
Inaccessible (Haz class 6.1), Domestic | USD 80+ |
Inaccessible (Haz class 6.1), International | USD 150+ |
Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |
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CAS No. : | 55341-62-3 | MDL No. : | MFCD20485912 |
Formula : | C14H7ClO2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 242.66 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Danger | Class: | 8 |
Precautionary Statements: | P501-P260-P270-P234-P271-P264-P280-P390-P362+P364-P303+P361+P353-P301+P330+P331-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P406-P405 | UN#: | 3261 |
Hazard Statements: | H302+H312+H332-H314-H290 | Packing Group: | Ⅲ |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: NaN3; acetone | ||
Multi-step reaction with 3 steps 1: aq. NaN3 / acetone 3: aq. HCl / ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | Stage #1: 3-aminosalicylic acid; 9-oxo-9H-fluorene-1-carbonyl chloride With triethylamine In dichloromethane at 0 - 20℃; for 4h; Stage #2: With hydrogenchloride In dichloromethane; water | 5.1.4. General procedure for the amide bond formation via acid chloride General procedure: To a stirred solution of amine (1.1 mmol, 1.1 equiv) and 0.46 mL triethylamine (3.3 mmol, dissolved in 2 mL dry CH2Cl2 at 0 °C, was added dropwise a solution of acid chloride (1 mmol, 1 equiv) in 2 mL dry CH2Cl2. Stirring was continued at 0 °C for 1 h and at room temperature for 3 h. The reaction mixture was diluted with 2-5 mL CH2Cl2, and acidified by 2 N HCl until pH 4. The precipitate was filtered, washed with H2O, CH2Cl2, and dried to give moderate-to-good yields (64-95%). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
1: 15% 2: 8% | Stage #1: 1,4-phenylenediamine-2-carboxylic acid; 9-oxo-9H-fluorene-1-carbonyl chloride With triethylamine In dichloromethane at 0 - 20℃; for 4h; Stage #2: With hydrogenchloride In dichloromethane; water | 5.1.4. General procedure for the amide bond formation via acid chloride General procedure: To a stirred solution of amine (1.1 mmol, 1.1 equiv) and 0.46 mL triethylamine (3.3 mmol, dissolved in 2 mL dry CH2Cl2 at 0 °C, was added dropwise a solution of acid chloride (1 mmol, 1 equiv) in 2 mL dry CH2Cl2. Stirring was continued at 0 °C for 1 h and at room temperature for 3 h. The reaction mixture was diluted with 2-5 mL CH2Cl2, and acidified by 2 N HCl until pH 4. The precipitate was filtered, washed with H2O, CH2Cl2, and dried to give moderate-to-good yields (64-95%). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | General procedure: To a stirred solution of amine (1.1 mmol, 1.1 equiv) and 0.46 mL triethylamine (3.3 mmol, dissolved in 2 mL dry CH2Cl2 at 0 C, was added dropwise a solution of acid chloride (1 mmol, 1 equiv) in 2 mL dry CH2Cl2. Stirring was continued at 0 C for 1 h and at room temperature for 3 h. The reaction mixture was diluted with 2-5 mL CH2Cl2, and acidified by 2 N HCl until pH 4. The precipitate was filtered, washed with H2O, CH2Cl2, and dried to give moderate-to-good yields (64-95%). |