Quinolines and derivatives
Aromatic organic heterocyclic compounds that contain a benzene ring fused with a six-membered ring that contains one nitrogen atom and five carbon atoms. Includes compounds that are derived from quinolines.
Quantity
- (1)
- (1)
- (1)
- (219)
- (6)
- (40)
- (2)
- (12)
- (47)
- (1)
- (37)
- (1)
- (2)
- (1)
- (1)
- (1)
- (4)
- (1)
- (1)
- (7)
- (132)
- (1)
- (9)
- (16)
- (1)
- (34)
- (1)
- (1)
- (1)
- (1)
- (1)
- (188)
- (1)
- (1)
- (15)
- (1)
- (17)
- (17)
- (7)
- (1)
Molecular Weight (g/mol)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (7)
- (21)
- (26)
- (2)
- (30)
- (4)
- (6)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (5)
- (2)
- (6)
- (5)
- (2)
- (1)
- (11)
- (1)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (25)
- (16)
- (2)
- (3)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (4)
- (4)
- (8)
- (2)
- (1)
- (2)
- (1)
- (1)
- (6)
- (2)
- (1)
- (1)
- (2)
- (1)
- (6)
- (1)
- (20)
- (1)
- (5)
- (1)
- (3)
- (5)
- (1)
- (2)
- (2)
- (2)
- (2)
- (8)
- (1)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (4)
- (2)
- (2)
- (1)
- (1)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (5)
- (1)
- (2)
- (5)
- (2)
- (4)
- (2)
- (3)
- (1)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (4)
- (2)
- (4)
- (1)
- (1)
- (3)
- (3)
- (1)
- (7)
- (2)
- (1)
- (4)
- (1)
- (1)
- (1)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (3)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (1)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (13)
- (1)
- (2)
- (2)
- (4)
- (3)
- (4)
- (1)
- (1)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (19)
- (2)
- (1)
- (2)
- (4)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (1)
- (4)
- (5)
- (1)
- (2)
- (1)
- (1)
- (2)
- (4)
- (3)
- (2)
- (1)
- (9)
- (5)
- (2)
- (3)
- (3)
- (2)
- (5)
- (6)
- (3)
- (13)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (3)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (4)
- (5)
- (4)
- (3)
- (3)
- (7)
- (1)
- (2)
- (3)
- (7)
- (5)
- (2)
- (1)
- (10)
- (1)
- (1)
Percent Purity
- (1)
- (2)
- (2)
- (4)
- (1)
- (2)
- (2)
- (4)
- (2)
- (2)
- (6)
- (2)
- (7)
- (4)
- (3)
- (2)
- (2)
- (5)
- (2)
- (1)
- (14)
- (1)
- (1)
- (23)
- (42)
- (24)
- (18)
- (83)
- (3)
- (17)
- (3)
- (5)
- (8)
- (1)
- (6)
- (1)
- (5)
- (1)
- (6)
- (5)
- (2)
- (5)
- (2)
- (6)
- (2)
- (2)
- (4)
- (1)
- (26)
- (19)
- (70)
- (109)
- (3)
- (1)
- (2)
- (59)
- (5)
- (1)
- (1)
Physical Form
- (2)
- (299)
- (2)
- (2)
- (25)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (3)
- (9)
- (3)
- (2)
- (62)
- (2)
- (5)
- (29)
- (3)
Boiling Point
- (1)
- (1)
- (3)
- (3)
- (2)
- (1)
- (2)
- (1)
- (5)
- (4)
- (2)
- (1)
- (3)
- (1)
- (2)
- (2)
- (5)
- (3)
- (2)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (12)
- (4)
- (1)
- (5)
- (3)
- (5)
- (2)
- (2)
- (3)
- (2)
- (1)
- (1)
- (3)
- (5)
- (1)
- (3)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
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691
ARCTOM SCIENTIFIC E-1-PIPERIDINO-3-3-QUINOLIN
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NC3720322 E-1-PIPERIDINO-3-3-QUINOLIN
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692
GRAINGER INC 7-METHYLQUINOLINE 25G
502781389 7-METHYLQUINOLINE 25G
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693
Ambeed tertButyl 1 8diazaspiro 4.5 de
tert-Butyl 1,8-diazaspiro[4.5]decane-8-carboxylate, 937729-06-1, 95%
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694
Ambeed 7Bromo3 4dihydroquinolin2 1H o
7-Bromo-3,4-dihydroquinolin-2(1H)-one, 14548-51-7, 97%
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695
Medchemexpress LLC 5'-O-(4,4'-dimethoxytrityl)-5-methoxyuridine | 2095417-73-3 | 98.2% | 576.59 g·mol⁻¹ | C31H32N2O9 | 10 MG
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5'-O-(4,4'-Dimethoxytrityl)-5-methoxyuridine is a DMT-protected nucleoside derivative used as a building block in solid-phase oligonucleotide synthesis. The 4,4'-dimethoxytrityl (DMT) group protects the 5'-hydroxyl during stepwise chain assembly, enabling incorporation of 5-methoxyuridine into synthetic oligonucleotides for research applications.
- DMT-protected 5'-hydroxyl for stepwise synthesis.
- Designed for incorporation into oligonucleotides.
- High purity suitable for research use (98.2%).
- Molecular weight 576.59 g·mol⁻¹.
- Chemical formula C31H32N2O9.
- Supplied as a small-scale vial (10 mg).
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696
Sigma Aldrich Fine Chemicals Biosciences Ethyl lactate 98 fCC fG25KG
Ethyl lactate is a major volatile flavor compound identified in Chinese Luzhou-flavor type liquor.
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697
Medchemexpress LLC Selenocystamine dih 5g
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Selenocystamine dihydrochloride is a selenocysteine derivative that can be used in the synthesis of other active compounds Selenocystamine dihydrochloride can also induce the aggregation of amphiphilic p-sulfonatocalixarene to form supramolecular nanoparticles[1][2][3]
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698
Ambeed Mono 6amino6deoxy cyclodextri
Mono-(6-amino-6-deoxy)-β-cyclodextrin, 29390-67-8, 95%
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699
Ambeed 3 Bromomethyl oxetane
3-(Bromomethyl)oxetane, 1374014-30-8, 95%
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700
Ambeed 5 6 7Trihydroxy2phenyl4Hchrome
5,6,7-Trihydroxy-2-phenyl-4H-chromen-4-one, 491-67-8, 96%
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701
Ambeed 4 6 2 3Methylbenzylidene hydra
4-(6-(2-(3-Methylbenzylidene)hydrazinyl)-2-(2-(pyridin-2-yl)ethoxy)pyrimidin-4-yl)morpholine dimethanesulfonate, 870087-36-8, 98%
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702
Ambeed Mono 6amino6deoxy cyclodextri
Mono-(6-amino-6-deoxy)-β-cyclodextrin, 29390-67-8, 95%
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703
Ambeed 3Aminopiperidine2 6dione
3-Aminopiperidine-2,6-dione, 2353-44-8, 98%
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704
Ambeed 11bR 2R 5R 1 Dinaphtho 2 1d
(11bR)-(2R,5R)-1-(Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-2,5-diphenylpyrrolidine, 444667-33-8, 98%
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705
Ambeed Methyl 6oxopiperidine2carboxyl
Methyl 6-oxopiperidine-2-carboxylate, 111479-60-8, 97%
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