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2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)

Base Information Edit
  • Chemical Name:2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)
  • CAS No.:130049-78-4
  • Molecular Formula:C10H9ClO2
  • Molecular Weight:196.633
  • Hs Code.:
  • Mol file:130049-78-4.mol
2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)

Synonyms:2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)

Suppliers and Price of 2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (2S)-3,4-Dihydro-2H-1-benzopyran-2-carbonylChloride
  • 1mg
  • $ 500.00
Total 3 raw suppliers
Chemical Property of 2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI) Edit
Chemical Property:
  • PSA:26.30000 
  • LogP:2.14560 
Purity/Quality:

98%min *data from raw suppliers

(2S)-3,4-Dihydro-2H-1-benzopyran-2-carbonylChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses (2S)-3,4-Dihydro-2H-1-benzopyran-2-carbonyl Chloride is an intermediate used in the synthesis of (S)-9-Hydroxy Risperidone-d4 (H953362), which is the S-enantiomer metabolite of Risperidone (R525000), a combined serotonin (5-HT2) and dopamine (D2) receptor antagonist.
Technology Process of 2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI)

There total 2 articles about 2H-1-Benzopyran-2-carbonylchloride,3,4-dihydro-,(2S)-(9CI) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With thionyl chloride; In 1,2-dichloro-ethane; at 0 ℃; for 1h; Reflux;
Guidance literature:
With thionyl chloride; N,N-dimethyl-formamide; In 1,2-dichloro-ethane; at 0 - 20 ℃; Reflux;
Refernces Edit
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