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323178-29-6

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  • 1,2,7-THIADIAZEPINE-2(3H)-ACETIC ACID, 7-[(1,1-DIMETHYLETHOXY)CARBONYL]-6,7-DIHYDRO-ALPHA-(PHENYLMETHYL)-, METHYL ESTER, 1,1-DIOXIDE,-(ALPHAS)

    Cas No: 323178-29-6

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  • 1,2,7-THIADIAZEPINE-2(3H)-ACETIC ACID,7-[(1,1-DIMETHYLETHOXY)CARBONYL]-6,7-DIHYDRO-A-BENZYL-,METHYL ESTER,1,1-DIOXIDE,-(AS)CAS

    Cas No: 323178-29-6

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323178-29-6 Usage

Chemical class

Thiadiazepine derivative

Explanation

Different sources of media describe the Explanation of 323178-29-6 differently. You can refer to the following data:
1. The compound belongs to the class of thiadiazepine derivatives, which are a type of heterocyclic compounds.
2. The compound is derived from thiadiazepine-2(3H)-acetic acid by replacing the carboxylic acid group with a methyl ester group.
3. The compound has a specific substituent attached to the thiadiazepine core, which is responsible for its unique properties and potential biological activity.
4. The compound contains a 1,1-dioxide group, which is an oxygen-containing functional group that can influence the compound's reactivity and stability.
5. The compound has a specific stereochemistry, with the phenylmethyl group being in the alpha position relative to the thiadiazepine core.
6. 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.
7. 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.
8. 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.

323178-29-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,7-THIADIAZEPINE-2(3H)-ACETIC ACID, 7-[(1,1-DIMETHYLETHOXY)CARBONYL]-6,7-DIHYDRO-α-(PHENYLMETHYL)-, METHYL ESTER, 1,1-DIOXIDE,-(ALPHAS)

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:323178-29-6 SDS

323178-29-6Relevant articles and documents

Amino acid-derived, 7-membered cyclic sulfamides and methods of synthesizing the same

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Example 3B, (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

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