323178-29-6 Usage
Chemical class
Thiadiazepine derivative
Explanation
The compound belongs to the class of thiadiazepine derivatives, which are a type of heterocyclic compounds.
Explanation
The compound is derived from thiadiazepine-2(3H)-acetic acid by replacing the carboxylic acid group with a methyl ester group.
Explanation
The compound has a specific substituent attached to the thiadiazepine core, which is responsible for its unique properties and potential biological activity.
Explanation
The compound contains a 1,1-dioxide group, which is an oxygen-containing functional group that can influence the compound's reactivity and stability.
Explanation
The compound has a specific stereochemistry, with the phenylmethyl group being in the alpha position relative to the thiadiazepine core.
Explanation
Due to its unique structure and potential biological activity, the compound may be of interest for research and development in the pharmaceutical and agricultural industries.
Explanation
The specific biological activity of the compound is not provided in the material, but its unique structure suggests that it may have potential applications in various fields.
Explanation
The compound's complex structure and potential biological activity make it a potentially important chemical for research and development in various industries.
Structure
Methyl ester derivative of thiadiazepine-2(3H)-acetic acid
Substituent
7-[(1,1-dimethylethoxy)carbonyl]-6,7-dihydro-alpha-(phenylmethyl)-
Functional group
1,1-dioxide
Stereochemistry
alphas (alpha stereochemistry)
Potential applications
Pharmaceutical and agricultural industries
Biological activity
Unknown
Research significance
Potentially important for research and development
Check Digit Verification of cas no
The CAS Registry Mumber 323178-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,3,1,7 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 323178-29:
(8*3)+(7*2)+(6*3)+(5*1)+(4*7)+(3*8)+(2*2)+(1*9)=126
126 % 10 = 6
So 323178-29-6 is a valid CAS Registry Number.
323178-29-6Relevant academic research and scientific papers
Amino acid-derived, 7-membered cyclic sulfamides and methods of synthesizing the same
-
, (2010/01/30)
New sulfamide compounds and methods of forming those compounds are provided. The inventive methods comprise subjecting a template opened-ring sulfamide compound to a ring-closing metathesis reaction in the presence of a Grubbs catalyst to yield a heterocyclic sulfamide. Advantageously, the template structures can be provided with a wide array of functional groups (e.g., substituted and unsubstituted amino acid side chains, peptides) chosen to provide particular properties to the compound. The preferred heterocyclic sulfamides are represented by a formula selected from the group consisting of
Ring-closing metathesis strategies to cyclic sulfamide peptidomimetics
Dougherty, Joseph M,Probst, Donald A,Robinson, Randall E,Moore, Joel D,Klein, Thomas A,Snelgrove, Kelley A,Hanson, Paul R
, p. 9781 - 9790 (2007/10/03)
Ring-closing metathesis (RCM) strategies toward the synthesis of a number of constrained sulfamides are discussed. This approach exploits the inherent chemistry of sulfamides and sulfonyl carbamates to generate both symmetric and unsymmetric cyclic sulfamides. Two strategies are revealed, one centers on the RCM reaction of allylated sulfamides 9a-e to generate the C2-symmetric cyclic sulfamides 4a-e in high yields. A second RCM strategy utilizes the known sulfonyl carbamate 15 to prepare unsymmetric cyclic sulfamides 16 and 6 in two four-step sequences. Overall, the routes described are applicable to the synthesis of a variety of constrained dipeptidal sulfamides representing novel peptidomimetic scaffolds. (C) 2000 Published by Elsevier Science Ltd.
