Welcome to LookChem.com Sign In|Join Free
  • or
(1S,4R,5S)-4-Phenyl-6,8-dioxa-3-thia-bicyclo[3.2.1]octane is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific stereochemistry, with the 1, 4, and 5 positions being in the S, R, and S configurations, respectively. The compound features a bicyclo[3.2.1]octane ring system, which is a type of bridged bicyclic structure with three carbons in one ring and two carbons in the other, connected by a bridge. Additionally, it contains a phenyl group attached to the 4-position, which contributes to its aromatic character, and a 6,8-dioxa-3-thia moiety, indicating the presence of two oxygen atoms and a sulfur atom in the ring, which imparts unique chemical properties. (1S,4R,5S)-4-Phenyl-6,8-dioxa-3-thia-bicyclo[3.2.1]octane is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other specialty chemicals due to its specific structural features.

87754-11-8

Post Buying Request

87754-11-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

87754-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87754-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,5 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87754-11:
(7*8)+(6*7)+(5*7)+(4*5)+(3*4)+(2*1)+(1*1)=168
168 % 10 = 8
So 87754-11-8 is a valid CAS Registry Number.

87754-11-8Downstream Products

87754-11-8Relevant academic research and scientific papers

Heterobicycles sulfures derives de l'α-thioglycerol. Synthese d'alkyl-2,8-dioxa-6-thiabicyclooctanes

Gelas, Jacques,Teppaz-Misson, Marc

, p. 1487 - 1493 (2007/10/02)

The synthesis of 2,8-dioxa-6-thiabicyclooctanes, substituted by alkyl or phenyl groups in positions 1, 4, or 7, is described.Four synthetic routes are compared: (i) action of sodium sulfide on 2,4-dichloro-1,3-dialkyldioxolanes; (ii) action of sodium sulfide on the ditosylates of 2,4-dihydroxyalkyl-1,3-dioxolanes; (iii) action of α-haloketones on α-thioglycerol; and (iv) action of α-hydroxyketones on α-thioglycerol.The structures of the dioxathiabicyclooctanes have been established by proton nmr (mass spectra have already been described) and chemically confirmed by desulfurization by Raney Nickel.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 87754-11-8