Naphthalenes
Polycyclic aromatic hydrocarbon compounds that consist of ten carbon atoms and eight hydrogen atoms fused into two benzene rings; it is the simplest polycyclic aromatic hydrocarbon.
Quantity
- (2)
- (1)
- (187)
- (9)
- (1)
- (28)
- (1)
- (10)
- (104)
- (3)
- (35)
- (6)
- (2)
- (1)
- (1)
- (2)
- (5)
- (1)
- (1)
- (1)
- (7)
- (241)
- (2)
- (12)
- (31)
- (24)
- (2)
- (1)
- (1)
- (203)
- (1)
- (1)
- (1)
- (18)
- (1)
- (11)
- (81)
- (1)
- (10)
- (1)
- (1)
Molecular Weight (g/mol)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (2)
- (17)
- (3)
- (13)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (5)
- (6)
- (9)
- (2)
- (8)
- (6)
- (28)
- (27)
- (1)
- (1)
- (10)
- (7)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (11)
- (24)
- (8)
- (6)
- (2)
- (5)
- (9)
- (2)
- (1)
- (2)
- (1)
- (1)
- (9)
- (2)
- (1)
- (5)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (16)
- (5)
- (7)
- (3)
- (2)
- (2)
- (13)
- (15)
- (2)
- (6)
- (1)
- (2)
- (2)
- (2)
- (4)
- (1)
- (2)
- (1)
- (6)
- (2)
- (1)
- (1)
- (8)
- (3)
- (4)
- (2)
- (10)
- (6)
- (3)
- (3)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (8)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (1)
- (4)
- (8)
- (3)
- (1)
- (8)
- (2)
- (1)
- (2)
- (9)
- (2)
- (9)
- (12)
- (1)
- (1)
- (14)
- (13)
- (1)
- (1)
- (1)
- (1)
- (5)
- (2)
- (1)
- (8)
- (8)
- (6)
- (2)
- (2)
- (4)
- (1)
- (3)
- (1)
- (1)
- (13)
- (7)
- (1)
- (1)
- (1)
- (2)
- (1)
- (10)
- (2)
- (4)
- (9)
- (1)
- (3)
- (3)
- (1)
- (4)
- (1)
- (13)
- (1)
- (1)
- (1)
- (4)
- (2)
- (1)
- (2)
- (1)
- (1)
- (2)
- (3)
- (4)
- (1)
- (1)
- (1)
- (4)
- (3)
- (2)
- (3)
- (4)
- (3)
- (1)
- (2)
- (3)
- (2)
- (2)
- (6)
- (2)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (1)
- (2)
- (2)
- (1)
- (1)
- (2)
- (4)
- (4)
- (2)
- (1)
- (2)
- (7)
- (5)
- (20)
- (3)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (3)
- (9)
- (2)
- (1)
- (2)
- (3)
- (2)
- (2)
- (1)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (2)
- (1)
- (1)
- (1)
- (5)
- (2)
- (4)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (1)
- (7)
- (1)
- (4)
- (2)
- (1)
- (3)
- (2)
- (1)
- (1)
- (4)
- (1)
- (4)
- (2)
- (1)
- (3)
- (1)
- (2)
- (3)
- (2)
- (2)
- (2)
- (1)
- (2)
- (4)
- (1)
- (1)
- (8)
- (3)
- (2)
- (1)
- (1)
- (2)
- (1)
- (2)
- (14)
- (1)
- (2)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (5)
- (2)
- (3)
- (5)
- (1)
- (1)
- (2)
- (4)
- (1)
- (8)
- (2)
- (2)
- (1)
- (1)
- (1)
- (4)
- (2)
- (2)
- (1)
- (2)
- (1)
- (2)
- (1)
- (1)
- (4)
- (1)
- (2)
- (1)
- (1)
Percent Purity
- (2)
- (2)
- (3)
- (2)
- (2)
- (2)
- (2)
- (3)
- (7)
- (2)
- (5)
- (1)
- (1)
- (1)
- (1)
- (1)
- (4)
- (1)
- (2)
- (3)
- (1)
- (2)
- (1)
- (3)
- (2)
- (7)
- (2)
- (2)
- (8)
- (2)
- (1)
- (9)
- (2)
- (4)
- (3)
- (1)
- (2)
- (12)
- (1)
- (11)
- (14)
- (2)
- (1)
- (1)
- (15)
- (9)
- (7)
- (28)
- (2)
- (61)
- (58)
- (30)
- (1)
- (13)
- (54)
- (2)
- (1)
- (36)
- (2)
- (2)
- (1)
- (2)
- (4)
- (2)
- (15)
- (1)
- (1)
- (3)
- (1)
- (2)
- (10)
- (1)
- (3)
- (3)
- (1)
- (3)
- (9)
- (11)
- (2)
- (3)
- (3)
- (30)
- (6)
- (95)
- (127)
- (3)
- (74)
- (12)
Physical Form
- (3)
- (3)
- (4)
- (440)
- (2)
- (8)
- (5)
- (1)
- (3)
- (4)
- (5)
- (6)
- (1)
- (1)
- (2)
- (28)
- (3)
- (6)
- (1)
- (97)
- (1)
- (1)
- (2)
- (2)
- (12)
- (5)
Boiling Point
- (4)
- (2)
- (1)
- (1)
- (1)
- (1)
- (2)
- (1)
- (2)
- (2)
- (2)
- (3)
- (1)
- (5)
- (1)
- (2)
- (1)
- (1)
- (2)
- (7)
- (1)
- (2)
- (2)
- (2)
- (2)
- (2)
- (1)
- (2)
- (3)
- (1)
- (1)
- (2)
- (1)
- (1)
- (2)
- (3)
- (4)
- (4)
- (3)
- (5)
- (3)
- (1)
- (3)
- (6)
- (3)
- (3)
- (5)
- (8)
- (2)
- (4)
- (2)
- (2)
- (2)
- (2)
- (1)
- (1)
- (1)
- (1)
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![eMolecules 131554-33-1 | 2-Benzothiazolylmagnesium bromide, 0.50 M in THF | Synthonix238.390 | C7H4BrMgNS | 0.000 | [Br-].[Mg+]c1nc2ccccc2s1 | 50ml | 702445851](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695046.jpg-250.jpg)
eMolecules 131554-33-1 | 2-Benzothiazolylmagnesium bromide, 0.50 M in THF | Synthonix238.390 | C7H4BrMgNS | 0.000 | [Br-].[Mg+]c1nc2ccccc2s1 | 50ml | 702445851
2-Benzothiazolylmagnesium bromide, 0.50 M in THF | Synthonix | 131554-33-1238.390 | C7H4BrMgNS | 0.000 | [Br-].[Mg+]c1nc2ccccc2s1 | 50ml | 702445851
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2,117
Aobchem AOBCHEM
5001075380 1 3-DIBROMO-5- 2-PROPEN-1-YL B
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2,118
Aobchem AOBCHEM
5001075381 1 3-DIBROMO-5- 2-PROPEN-1-YL B
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2,119
Aobchem AOBCHEM
5001076524 MORPHOLINO NAPHTHALEN-2-YL MET
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2,120
Aobchem AOBCHEM
5001075628 1-BROMO-4- 2-PROPEN-1-YLSULFON
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2,121
Aobchem AOBCHEM
5001075852 4- 4-BROMOPHENYL METHOXY -1-C
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2,122
EMOLECULES INC 5-TRIBUTYLSTANNYLTHIAZOLE 1G
502696601 5-TRIBUTYLSTANNYLTHIAZOLE 1G
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2,123
MEDCHEMEXPRESS LLC 1 4-CHRYSENEQUINONE 50MG
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501872322 1 4-CHRYSENEQUINONE 50MG
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2,124
MEDCHEMEXPRESS LLC MENADIONE 500MG
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501874086 MENADIONE 500MG
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2,125
MEDCHEMEXPRESS LLC OXANTEL PAMOATE 100MG
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501874510 OXANTEL PAMOATE 100MG
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2,126
Aobchem 1-Chloro-4-nitronaphthalene | ≥97% | CAS 605-61-8 | C10H6ClNO2 | 25g
1-Chloro-4-nitronaphthalene | ≥97% | CAS 605-61-8 | C10H6ClNO2 | 25g
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2,127
Medchemexpress LLC Tetracaine hydrochloride | 136-47-0 | 99.91% | 1 G
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Tetracaine hydrochloride (Amethocaine hydrochloride) is a calcium channel protein inhibitor that blocks voltage-sensitive release of Ca2+ from the sarcoplasmic reticulum. It is primarily used topically in ophthalmology and as an antipruritic. It also alters the function of calcium release channels (ryanodine receptors) that regulate calcium release from intracellular stores.
- Blocks voltage-sensitive release of Ca2+ from the sarcoplasmic reticulum.
- Used topically in ophthalmology.
- Acts as an antipruritic.
- Alters the function of calcium release channels (ryanodine receptors).
- Inhibits spontaneous calcium release events at low concentrations.
- Completely blocks calcium release at high concentrations.
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2,128
Medchemexpress LLC Amorolfine hydrochloride | 78613-38-4 | MFCD00903738 | 99.8% | 1 ML
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Amorolfine hydrochloride (Ro 14-4767/002) is a potent antifungal agent that inhibits ergosterol biosynthesis, a crucial component of fungal cell membranes. This mechanism of action makes it effective against a broad spectrum of fungi. It holds potential for research into *Neoscytalidium dimidiatum* onychomycosis and other fungal infections.
- Potent antifungal agent
- Inhibits ergosterol biosynthesis
- Effective against a broad spectrum of fungi
- Potential for research into onychomycosis
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2,129
![eMolecules 29046-78-4 | Nickel(II) chloride, dimethoxyethane adduct, min. 97% | Strem Chemicals | MFCD00013481 | 219.720 | C4H10Cl2NiO2 | 97.000 | [Cl-].[Cl-].[Ni++].COCCOC | 25g | 321342037](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502697941.jpg-250.jpg)
eMolecules 29046-78-4 | Nickel(II) chloride, dimethoxyethane adduct, min. 97% | Strem Chemicals | MFCD00013481 | 219.720 | C4H10Cl2NiO2 | 97.000 | [Cl-].[Cl-].[Ni++].COCCOC | 25g | 321342037
Nickel(II) chloride, dimethoxyethane adduct, min. 97% | Strem Chemicals | 29046-78-4 | MFCD00013481 | 219.720 | C4H10Cl2NiO2 | 97.000 | [Cl-].[Cl-].[Ni++].COCCOC | 25g | 321342037
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2,130
![eMolecules 926-62-5 | Isobutylmagnesium bromide, 1.0 M in THF | Synthonix | MFCD00075126 | 161.325 | C4H9BrMg | 0.000 | [Br-].CC(C)C[Mg+] | 50ml | 702445924](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502694982.jpg-250.jpg)
eMolecules 926-62-5 | Isobutylmagnesium bromide, 1.0 M in THF | Synthonix | MFCD00075126 | 161.325 | C4H9BrMg | 0.000 | [Br-].CC(C)C[Mg+] | 50ml | 702445924
Isobutylmagnesium bromide, 1.0 M in THF | Synthonix | 926-62-5 | MFCD00075126 | 161.325 | C4H9BrMg | 0.000 | [Br-].CC(C)C[Mg+] | 50ml | 702445924
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