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1,4-Dithia-7-azaspiro[4,4]nonane-8-carboxylic acid hydrobromide is a complex heterocyclic compound characterized by a ring structure containing carbon, sulfur, nitrogen, and hydrogen atoms. The spiro configuration denotes two rings sharing a common atom, and the hydrobromide derivative indicates the presence of bromine. As a synthetic compound, it is primarily recognized for its applications in pharmaceuticals and research, although its specific uses are not extensively documented.

75776-79-3

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75776-79-3 Usage

Uses

Used in Pharmaceutical Industry:
1,4-Dithia-7-azaspiro[4,4]nonane-8-carboxylic acid hydrobromide is used as a research compound for its potential applications in drug development. Its unique structure and reactivity with other compounds make it a valuable candidate for exploring new therapeutic agents.
Used in Research Applications:
1,4-Dithia-7-azaspiro[4,4]nonane-8-carboxylic acid hydrobromide is used as a chemical intermediate in the synthesis of other complex molecules. Its properties and interactions with other compounds can provide insights into the development of new chemical entities and their potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 75776-79-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,7 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75776-79:
(7*7)+(6*5)+(5*7)+(4*7)+(3*6)+(2*7)+(1*9)=183
183 % 10 = 3
So 75776-79-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2S2.BrH/c9-6(10)5-3-7(4-8-5)11-1-2-12-7;/h5,8H,1-4H2,(H,9,10);1H/t5-;/m0./s1

75776-79-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Dithia-7-azaspiro[4,4]nonane-8-carboxylic acid hydrobromide

1.2 Other means of identification

Product number -
Other names 1,4-DITHIA-7-AZASPIRO[4,4]NONANE-8-CARBOXYLIC ACID HYDROBROMIDE,(S)

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:75776-79-3 SDS

75776-79-3Downstream Products

75776-79-3Relevant academic research and scientific papers

Angiotensin Converting Enzyme Inhibitors: Spirapril and Related Compounds

Smith, Elizabeth M.,Swiss, Gerald F.,Neustadt, Bernard R.,McNamara, Paul,Gold, Elijah H.,et al.

, p. 1600 - 1606 (2007/10/02)

The synthesis of spirapril (5), spiraprilat (25), their RSS stereoisomers, and their glycyl (18b) and lysyl (36, 37) analogues is described.These compounds were evaluated in vivo for inhibition of angiotensin converting enzyme (ACE), and selected compounds were evaluated for in vitro ACE inhibition (spirapril ID50 16 μg/kg; spiraprilat IC50 0.8 nM, ID50 8 μg/kg).In anesthetized rats, iv, esters 5 and 36 are more potent than enalapril, and diacids 25 and 37 are more potent than enalaprilat in vitro.In the conscious rats, orally, 5 and enalapril (2) showed potent and sustained activity at doses of 0.03-1 and 0.1-1 mg/kg, respectively.From this work, spirapril was selected for clinical evaluation as an antihypertensive agent.

7-Carboxyalkylaminoacyl-1,4-dithia-7-azaspiro[4.4]-nonane-8-carboxylic acids

-

, (2008/06/13)

This invention relates to 7-carboxyalkyl-aminoacyl-1,4-adithia-7-azaspiro[4.4]nonane-8-carboxylic acids. The compounds of the invention are useful in the treatment of cardiovascular disorders and especially as antihypertensive agents.

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