Home Cart 0 Sign in  

[ CAS No. 55341-62-3 ]

{[proInfo.proName]} ,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

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+
Chemical Structure| 55341-62-3
Chemical Structure| 55341-62-3
Structure of 55341-62-3 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Bulk Inquiry Add To Cart

Quality Control of [ 55341-62-3 ]

Related Doc. of [ 55341-62-3 ]

Alternatived Products of [ 55341-62-3 ]

Product Details of [ 55341-62-3 ]

CAS No. :55341-62-3 MDL No. :MFCD20485912
Formula : C14H7ClO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :242.66 Pubchem ID :-
Synonyms :

Safety of [ 55341-62-3 ]

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:
GHS Pictogram:

Application In Synthesis of [ 55341-62-3 ]

* 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.

  • Downstream synthetic route of [ 55341-62-3 ]

[ 55341-62-3 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 55341-62-3 ]
  • [ 6344-62-3 ]
YieldReaction ConditionsOperation 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
  • 2
  • [ 55341-62-3 ]
  • [ 1514-16-5 ]
  • 3
  • [ 2836-03-5 ]
  • [ 55341-62-3 ]
  • N-(2-dimethylaminophenyl)-9-oxo-9H-fluorene-1-carboxamide [ No CAS ]
  • 4
  • [ 570-23-0 ]
  • [ 55341-62-3 ]
  • [ 1133971-01-3 ]
YieldReaction ConditionsOperation 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%).
  • 5
  • [ 610-74-2 ]
  • [ 55341-62-3 ]
  • [ 1133970-96-3 ]
  • [ 1133971-25-1 ]
YieldReaction ConditionsOperation 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%).
  • 6
  • [ 108679-71-6 ]
  • [ 55341-62-3 ]
  • [ 1133971-24-0 ]
YieldReaction ConditionsOperation 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%).
Same Skeleton Products
Historical Records