164359-75-5 Usage
Explanation
The compound's systematic name, indicating its structure and classification.
Explanation
The compound contains a thiazepine ring, which is a heterocyclic ring with sulfur and nitrogen atoms.
Explanation
The compound has a carboxaldehyde group (-CHO) attached to one of the carbon atoms in the thiazepine ring.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), nitrogen (N), oxygen (O), and sulfur (S) atoms in the compound.
Explanation
The molecular weight is the sum of the atomic weights of all the atoms in the molecule.
Explanation
The compound's structure and properties make it a candidate for further research in the development of pharmaceuticals and as an intermediate in organic synthesis.
Explanation
The compound's properties, such as its stability and reactivity, make it a valuable subject for further study and potential commercial applications.
Explanation
The compound's structure is characterized by a six-membered thiazepine ring containing a sulfur and nitrogen atom, with a carboxaldehyde group attached to one of the carbon atoms.
Heterocyclic Compound
Yes
Carboxaldehyde Functional Group
Present
Molecular Weight
155.21 g/mol
Potential Applications
Pharmaceuticals and Organic Synthesis
Chemical and Physical Properties
Suitable for Research and Industrial Uses
Structure
Six-membered ring with a sulfur and nitrogen atom, and a carboxaldehyde group attached
Check Digit Verification of cas no
The CAS Registry Mumber 164359-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,3,5 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 164359-75:
(8*1)+(7*6)+(6*4)+(5*3)+(4*5)+(3*9)+(2*7)+(1*5)=155
155 % 10 = 5
So 164359-75-5 is a valid CAS Registry Number.
164359-75-5Relevant academic research and scientific papers
Federsel,Glasare,Hogstrom,Wiestal,Zinko,Odman
, p. 2597 - 2606 (1995)
A straightforward, two-step sequence capable of converting simple thiazoles into different sets of ring-expanded N,S-heterocycles of various sizes has been developed. The initial quaternizations of the heterocyclic moieties conducted with α,ω-dihaloalkanes (chain lengths from 2 to 8) in a 1:5 stoichiometry, afford the monoquaternary intermediates in isolated yields ranging from 16-71% (benzothiazole series, 9) to 17-93% (thiazole series, 10), respectively. In the subsequent OH--induced rearrangement, an expeditious ring-opening/ring-closure event incorporates the previously attached alkyl side chain in the newly formed hetero ring. Here the yields of benzannelated products 11 lie in the interval from 39 to 82%, while the monocyclic counterparts 12 fall within 11 to 59%, which in an overall perspective makes this methodology preparatively significant for an array of new compounds up to (at least) 12-membered ring sizes.
