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Home/Compounds/Pharmaceutical Intermediate/Methyl (1R,2R,4S)-2-[(5-hexen-1-ylmethylamino)carbonyl]-4-[[7-methoxy-8-methyl-2-[4-(1-methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]cyclopentanecarboxylate
C32H41N3O5S
579.8 g/mol
Pharmaceutical IntermediateWarning

Methyl (1R,2R,4S)-2-[(5-hexen-1-ylmethylamino)carbonyl]-4-[[7-methoxy-8-methyl-2-[4-(1-methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]cyclopentanecarboxylate

CAS1042695-87-3
Category
Pharmaceutical Intermediate
Compound Class
Heterocycle
Primary Use
Pharmaceutical Intermediate

This compound is a complex organic molecule featuring a cyclopentanecarboxylate core with multiple functional groups, including an amide, an ester, ether linkages, and a heterocyclic thiazole-substituted quinoline system. It is primarily utilized as a pharmaceutical intermediate in research and manufacturing.

Pharmaceutical intermediate for organic synthesisResearch compound for drug developmentBuilding block in medicinal chemistry

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Safety Reference

Harmful
Harmful
Environmental Hazard
Environmental Hazard
Warning
H302Harmful if swallowed
H413May cause long lasting harmful effects to aquatic life

Customs Tariff Classification

The international HS code for Methyl (1R,2R,4S)-2-[(5-hexen-1-ylmethylamino)carbonyl]-4-[[7-methoxy-8-methyl-2-[4-(1-methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]cyclopentanecarboxylate (CAS 1042695-87-3) is 2934.10.

HS code (international, 6-digit)

2934.10

EU CN code (8-digit)

2934 10 00

Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.

Identifiers
IUPAC Name

methyl (1R,2R,4S)-2-[hex-5-enyl(methyl)carbamoyl]-4-[7-methoxy-8-methyl-2-(4-propan-2-yl-1,3-thiazol-2-yl)quinolin-4-yl]oxycyclopentane-1-carboxylate

InChIKey

OHDHGPWHGQPFCD-QPTUXGOLSA-N

SMILES

CC1=C(C=CC2=C1N=C(C=C2O[C@H]3C[C@H]([C@@H](C3)C(=O)OC)C(=O)N(C)CCCCC=C)C4=NC(=CS4)C(C)C)OC

Synonyms (4)

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