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111188-71-7

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111188-71-7 Usage

Chemical structure

A compound with a benzothiazepinone core, an acetyloxy group at position 3, a dimethylaminoethyl group at position 5, and a 4-methoxyphenyl group at position 2.

Stereochemistry

The compound has a (2R-trans)configuration, indicating the arrangement of atoms in three-dimensional space.

Potential pharmacological properties

The structure of the compound suggests that it may have potential pharmacological properties, making it a candidate for further research and development.

Drug development

The compound's structure could be used as a basis for the development of new drugs targeting specific biological pathways.

Molecular weight

The molecular weight of the compound is approximately 408.5 g/mol.

Functional groups

The compound contains several functional groups, including an acetyloxy group, a dimethylamino group, and a methoxy group.

Stability

The stability of the compound under different conditions (e.g., temperature, pH, light exposure) may be influenced by its chemical structure and functional groups.

Synthesis

The synthesis of the compound may involve multiple steps, including the formation of the benzothiazepinone core, introduction of the acetyloxy group, attachment of the dimethylaminoethyl group, and incorporation of the 4-methoxyphenyl group.

Biological activity

The compound's potential biological activity may be investigated through in vitro and in vivo assays to determine its efficacy and safety as a drug candidate.

Structure-activity relationship (SAR)

The study of the relationship between the compound's structure and its biological activity can help guide the design of more potent and selective drug candidates.

Patentability

The compound's unique structure and potential pharmacological properties may make it eligible for patent protection, providing an incentive for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 111188-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,8 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111188-71:
(8*1)+(7*1)+(6*1)+(5*1)+(4*8)+(3*8)+(2*7)+(1*1)=97
97 % 10 = 7
So 111188-71-7 is a valid CAS Registry Number.

111188-71-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3S)-3-acetoxy-5-<2-(dimethylamino)ethyl>-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one

1.2 Other means of identification

Product number -
Other names Acetic acid (2R,3S)-5-(2-dimethylamino-ethyl)-2-(4-methoxy-phenyl)-4-oxo-2,3,4,5-tetrahydro-benzo[b][1,4]thiazepin-3-yl ester

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:111188-71-7 SDS

111188-71-7Relevant articles and documents

Stereoselective addition of 2-aminothiophenol to α-alkoxycinnamic acid derivatives - Alternative synthesis of (±)-diltiazem

Miyata, Okiko,Shinada, Tetsuro,Naito, Takeaki,Ninomiya, Ichiya,Date, Tadamasa,Okamura, Kimio

, p. 8119 - 8128 (2007/10/02)

A stereocontrolled synthesis of (±)-diltiazem by applying nucleophilic addition of 2-aminothiophenol to α-alkoxycinnamic acid derivatives is described.

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