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Cis-4-phenylthio-L-proline, also known as Zofenopril Intermediate, is a key chemical intermediate used in the synthesis of the angiotensin-converting enzyme (ACE) inhibitor Zofenopril. It features a proline backbone with a phenylthio group attached to the fourth position, contributing to the pharmacological properties of Zofenopril as an effective ACE inhibitor. This thiol-containing compound is synthesized through a series of chemical reactions and plays a crucial role in the pharmaceutical manufacturing process of Zofenopril, which is utilized in the treatment of high blood pressure and congestive heart failure.

81653-77-2

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81653-77-2 Usage

Uses

Used in Pharmaceutical Industry:
Cis-4-phenylthio-L-proline (Zofenopril Intermediate) is used as a key intermediate in the synthesis of Zofenopril for its role in the treatment of high blood pressure and congestive heart failure. As an ACE inhibitor, Zofenopril helps regulate blood pressure by inhibiting the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor, thus promoting vasodilation and reducing the workload on the heart.
Used in Medicinal Chemistry Research:
Cis-4-phenylthio-L-proline (Zofenopril Intermediate) serves as a valuable compound in medicinal chemistry research for the development of new ACE inhibitors or other related pharmaceuticals. Its unique structure and properties make it a promising candidate for further exploration and modification to improve the efficacy and safety of treatments for cardiovascular diseases.
Used in Drug Manufacturing Process:
Cis-4-phenylthio-L-proline (Zofenopril Intermediate) is utilized in the drug manufacturing process as an essential component in the production of Zofenopril. Its synthesis and incorporation into the final drug product are critical steps in ensuring the therapeutic effectiveness of Zofenopril in managing high blood pressure and congestive heart failure.

Check Digit Verification of cas no

The CAS Registry Mumber 81653-77-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81653-77:
(7*8)+(6*1)+(5*6)+(4*5)+(3*3)+(2*7)+(1*7)=142
142 % 10 = 2
So 81653-77-2 is a valid CAS Registry Number.

81653-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4S)-4-phenylsulfanylpyrrolidine-2-carboxylic acid

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:81653-77-2 SDS

81653-77-2Upstream product

81653-77-2Relevant academic research and scientific papers

PROLINE DERIVATIVES HAVING AFFINITY FOR THE CALCIUM CHANNEL ALPHA-2-DELTA SUBUNIT

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Page/Page column 48, (2010/02/06)

The compounds of formula (I) or a pharmaceutically acceptable salt, solvate or pro-drug thereof, are proline derivatives useful in the treatment of epilepsy, faintness attacks, hypokinesia, cranial disorders, neurodegenerative disorders, depression, anxiety, panic, pain, fibromyalgia, arthritis, neuropathalogical disorders, sleep disorders, visceral pain disorders and gastrointestinal disorders. Processes for the preparation of the final products and intermediates useful in the process are included. Pharmaceutical compositions containing one or more of the compounds are also included. Wherein either X is O, S, NH or CH2 and Y is CH2 or a direct bond, or Y is O, S or NH and X is CH2; and R is a 3-12 membered cycloalkyl, 4-12 membered heterocycloalkyl, heteroaryl or aryl, where any ring may be optionally substituted with one or more substituents independently selected from halogen, hydroxy, cyano, nitro, amino, hydroxycarbonyl, Cl-C6 alkyl, Cl-C6 alkenyl, CI-C6 alkynyl, Cl-C6 alkoxy, hydroxyC,-C6 alkyl, Cl-C6 alkoxyC,-C6 alkyl, perfluoro Cl-C6 alkyl, perfluoroC,-C6 alkoxy, Cl-C6 alkylamino, di- C1-C6 alkylamino, aminoC1-C6 alkyl, Cl-C6 alkylaminoC,-C6 alkyl, di-Cl-C6 alkylaminoC,-C6 alkyl, CI-C6acyl, C1-C6acyloxy, Cl-C6acyloxyC,-C6 alkyl, Cl-C6 acylamino, Cl-C6 alkylthio, C1-C6 alkylthiocarbonyl, C1-C6 alkylthioxo, C1-C6 alkoxycarbonyl, Cl-C6 alkylsulfonyl, C1-C6 alkylsulfonylamino, aminosulfonyl, Cl-C6 alkylaminosulfonyl, di-Cl-C6 alkylaminosulfonyl, 3-8 membered cycloalkyl, 4-8 membered heterocycloalkyl, phenyl and monocyclic heteroaryl; or a pharmaceutically acceptable salt, solvate or pro-drug thereof.

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