Welcome to LookChem.com Sign In|Join Free
  • or
6H-1,3-Thiazine-5-methanol, 2-phenyl- is a chemical compound with the molecular formula C11H11NOS. It is a derivative of 1,3-thiazine, a heterocyclic compound consisting of a six-membered ring with one sulfur atom and one nitrogen atom. The 2-phenyl substitution indicates the presence of a phenyl group (C6H5) attached to the second carbon atom of the thiazine ring. 6H-1,3-Thiazine-5-methanol, 2-phenyl- is an alcohol, as it contains a hydroxyl group (-OH) attached to the fifth carbon atom of the thiazine ring. Due to its unique structure, 6H-1,3-Thiazine-5-methanol, 2-phenyl- may exhibit various chemical properties and potential applications in pharmaceuticals, agrochemicals, or other industrial sectors.

82461-91-4

Post Buying Request

82461-91-4 Suppliers

Recommended suppliers

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

82461-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82461-91-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,6 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82461-91:
(7*8)+(6*2)+(5*4)+(4*6)+(3*1)+(2*9)+(1*1)=134
134 % 10 = 4
So 82461-91-4 is a valid CAS Registry Number.

82461-91-4Downstream Products

82461-91-4Relevant academic research and scientific papers

REGIOSELECTIVE ELECTROREDUCTION OF 6H-1,3-THIAZINES. COMPARISON WITH CHEMICAL REDUCTIONS I - INVESTIGATION OF 2-PHENYL-6H-1,3-THIAZINES

Bujoli, Bruno,Jubault, Michel,Roze, Jean-Claude,Tallec, Andre

, p. 2709 - 2720 (2007/10/02)

The electrochemical reduction of 2-phenyl-6H-1,3-thiazines carried out at a mercury cathode in acetate buffer + ethanol (1:1) has been studied: - In the case of compounds monoactivated at carbon 5 (R5 = CHO or COCH3) either hydrodimers (resulti

Reduction Regioselective de Phenyl-2 6H-Thiazines-1,3 Substituees en 5 par des Groupements Fonctionnels Electroattracteurs

Pradere, Jean-Paul,Roze, Jean-Claude,Duguay, Guy

, p. 901 - 911 (2007/10/02)

Sodium cyanoborohydride, triethylsilane (acidic medium), and aluminium amalgam (basic medium) regioselectively reduce the intracyclic imine group whereas sodium borohydride transforms the carbonyl fonction at position 5 into an alcohol.

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 82461-91-4