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Chemical Structure| 34967-61-8 Chemical Structure| 34967-61-8

Structure of 34967-61-8

Chemical Structure| 34967-61-8

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Product Details of [ 34967-61-8 ]

CAS No. :34967-61-8
Formula : C6H4Cl2O2S
M.W : 211.07
SMILES Code : O=C(O)CC1=C(Cl)SC(Cl)=C1

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Application In Synthesis of [ 34967-61-8 ]

* 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 [ 34967-61-8 ]

[ 34967-61-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6964-21-2 ]
  • [ 34967-61-8 ]
YieldReaction ConditionsOperation in experiment
72% With N-chloro-succinimide; In acetic acid; at 20℃; for 12h; A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol) in acetic acid (10 mL) was treated with N-chlorosuccinimide (3. 1 g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2, 5-dichlorothien-3-vl) acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ( [M-H]-).
72% With N-chloro-succinimide; In acetic acid; at 20℃; for 12h; A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol} in acetic acid (10 mL) was treated with N-chlorosuccinimide (3. 1g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2. 5-dichlorothien-3-yl) acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ( [M-H]-).
72% With N-chloro-succinimide; In acetic acid; at 20℃; for 12h; Step 1: A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol) in acetic acid (10 mL) was treated with N-chlorosuccinimide (3. 1g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2, 5-dichlorothien-3-yl) acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ( [M-H]-).
72% With N-chloro-succinimide; In acetic acid; at 20℃; for 12h; Example 141: 1-(2, 5-dichlorothien-3-vl)-2-piperazine-1-ylethyllcyclohexanol dihvdrochloride [0391] Step 1: A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol) in acetic acid (10 mL) was treated with N-chlorosuccinimide (3. 1g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2. 5-dichlorothien-3-yl) acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ( [M-H]-).
72% With N-chloro-succinimide; In acetic acid; at 20℃; for 12h; A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol) in acetic acid (10 mL) was treated with N-chlorosuccinimide (3. 1g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2. 5-dichlorothien-3-yl) acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ( [M-H]-).

  • 2
  • [ 6964-21-2 ]
  • [ 128-09-6 ]
  • [ 34967-61-8 ]
YieldReaction ConditionsOperation in experiment
72% In acetic acid; at 20℃; for 12h; A solution of 3-thiophene acetic acid (1.42 g, 10.0 mmol) in acetic acid (10 mL) was treated with N-chlorosuccinimide (3.1 g, 23 mmol, 2.3 equivalents), and the solution was stirred for 12 h at room temperature then concentrated in vacuo. The residue was diluted with water and stirred for 1 h whereupon the resulting solid was collected by filtration. The solid was dried in a vacuum oven at room temperature for 10 hours providing 1.51 g (72%) of (2,5-dichlorothien-3-yl)acetic acid as a brown solid, which was used as such in the next step. MS (ESI) m/z 209/211/213 ([M-H]-).
 

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