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PG 501

PG 501 structure

CAS No.: 32891-29-5

Chemical Name:: PG 501

Synonyms: PG 501;Pentona;KAO 264;mazaticol hydrochloride;9-Azabicyclo[3.3.1]nonane, 2-thiopheneacetic acid deriv.;6,6,9-Trimethyl-9-azabicyclo[3.3.1]non-3b-yl a,a-di(2-thienyl)glycolate hydrochloride;6,6,9-Trimethyl-9-azabicyclo[3.3.1]nonan-3b-ol a,a-di-2-thienylglycolate (ester) hydrochloride;Glycolic acid, di-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester hydrochloride, exo- (8CI);2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, exo-;2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, (1R,3R,5R)-6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, rel- (9CI)

CBNumber:: CB61269985

Molecular Formula:: C21H27NO3S2.HCl

Molecular Weight:: 0

MDL Number:: MFCD01680282

MOL File:: 32891-29-5.mol

Last updated:2023-05-04 17:34:37

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PG 501 Properties

FDA UNII	44WQI5180Q

PG 501 price

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
American Custom Chemicals Corporation	API0003264	PG 501 95.00%	32891-29-5	5MG	$497.87	2021-12-16	Buy

Product number	Packaging	Price	Buy
API0003264	5MG	$497.87	Buy

PG 501 Chemical Properties,Uses,Production

Originator

Pentona, Tanabe ,Japan ,1978

Definition

ChEBI: Mazaticol hydrochloride is an organic molecular entity.

Manufacturing Process

A mixture of 1.0 g of 6,6,9-trimethyl-9-azabicyclo[3.3.1]nonan-3β-ol, methyl α,α-di-(2-thienyl)-glycolate and 30 mg of metallic sodium is heated at 80°C to 90°C for about 2 hours under reduced pressure. After cooling, ether is added to the reaction mixture. The mixture is extracted with 10% hydrochloric acid. The aqueous layer is alkalified with sodium carbonate and reextracted with ethyl acetate. The extract is washed with water, dried and concentrated to dryness. The residue thus obtained is treated with hydrogen chloride by conventional manner. 2.0 g of the α,α-di-(2-thienyl)glycolate of 6,6,9- trimethyl-9-azabicyclo[3.3.1]nonan-3β-ol hydrochloride are obtained. Yield 83%.

Therapeutic Function

Antiparkinsonian

PG 501 Preparation Products And Raw materials

Raw materials

Preparation Products

PG 501 Suppliers

Global( 2)Suppliers

Supplier	Tel	Email	Country	ProdList	Advantage
TargetMol Chemicals Inc.	+1-781-999-5354	support@targetmol.com	United States	19973	58

Supplier	Advantage
TargetMol Chemicals Inc.	58

32891-29-5(PG 501)Related Search:

Methyl 2,2-dithienylglycolate (1S)-1-(2-THIENYL)ETHANOL Methyl 2-thienylacetate 2-HYDROXY-2,2-BIS(2-THIENYL) ACETIC ACID Ethyl 2-thiopheneacetate

PG 501 2-(Thiophen-2-yl)propan-2-ol (S)-2-(Hydroxyethyl)piperidine hydrochloride (1R)-1-(2-THIENYL)ETHANOL

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2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, (1R,3R,5R)-6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, rel- (9CI) 2-Thiopheneacetic acid, a-hydroxy-a-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester, hydrochloride, exo- 6,6,9-Trimethyl-9-azabicyclo[3.3.1]non-3b-yl a,a-di(2-thienyl)glycolate hydrochloride 6,6,9-Trimethyl-9-azabicyclo[3.3.1]nonan-3b-ol a,a-di-2-thienylglycolate (ester) hydrochloride 9-Azabicyclo[3.3.1]nonane, 2-thiopheneacetic acid deriv. Glycolic acid, di-2-thienyl-, 6,6,9-trimethyl-9-azabicyclo[3.3.1]non-3-yl ester hydrochloride, exo- (8CI) KAO 264 mazaticol hydrochloride PG 501 Pentona 32891-29-5 C21H27NO3S2HCl