Methyl 6-bromo-2-naphthoate

Modify Date: 2025-08-25 17:31:09

Methyl 6-bromo-2-naphthoate structure	Common Name	Methyl 6-bromo-2-naphthoate
	CAS Number	33626-98-1	Molecular Weight	265.103
	Density	1.5±0.1 g/cm3	Boiling Point	357.0±15.0 °C at 760 mmHg
	Molecular Formula	C₁₂H₉BrO₂	Melting Point	123-126 °C(lit.)
	MSDS	Chinese USA	Flash Point	169.7±20.4 °C

Name	methyl 6-bromonaphthalene-2-carboxylate
Synonym	More Synonyms

Density	1.5±0.1 g/cm3
Boiling Point	357.0±15.0 °C at 760 mmHg
Melting Point	123-126 °C(lit.)
Molecular Formula	C₁₂H₉BrO₂
Molecular Weight	265.103
Flash Point	169.7±20.4 °C
Exact Mass	263.978577
PSA	26.30000
LogP	4.20
Vapour Pressure	0.0±0.8 mmHg at 25°C
Index of Refraction	1.635

Methyl 6-bromo-2-naphthoate MSDS(Chinese)

Personal Protective Equipment	Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes	C: Corrosive;
Risk Phrases	R20/21/22
Safety Phrases	S24/25
RIDADR	NONH for all modes of transport
WGK Germany	3
HS Code	2916399090

Precursor 6
CAS#:67-56-1 Methanol CAS#:5773-80-8 6-Bromo-2-napht... CAS#:186581-53-3 diazomethane CAS#:15231-91-1 6-Bromo-2-naphthol
CAS#:201230-82-2 carbon monoxide CAS#:151600-02-1 6-Bromo-2-napht...
DownStream 10
CAS#:5773-80-8 6-Bromo-2-napht... CAS#:932033-57-3 2,2'-Bis-(1-ada... CAS#:106685-41-0 Mehtyl 6-[3-(1-... CAS#:100751-63-1 6-BROMO-2-NAPHT...
CAS#:32721-06-5 2-(6-Bromonapht... CAS#:305798-03-2 2-(6-bromonapht... CAS#:106685-40-9 Adapalene CAS#:170737-46-9 6-Bromo-2-napht...
CAS#:736989-93-8 Methyl 6-(4,4,5... CAS#:855207-53-3 6-Phenylnaphtha...

HS Code	2916399090
Summary	2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Synthesis, structure-affinity relationships, and biological activities of ligands binding to retinoic acid receptor subtypes.

J. Med. Chem. 38(26) , 4993-5006, (1995)

The retinoic acid receptors (RARs) transduce retinoid dependant gene regulation, and many biological effects of retinoids are mediated through binding and activation of three closely related receptor ...

Synthesis and fluorosolvatochromism of 3-arylnaphtho[1,2-b]quinolizinium derivatives.

Beilstein J. Org. Chem. 12(1) , 854-62, (2016)

Cationic biaryl derivatives were synthesized by Suzuki-Miyaura coupling of 3-bromonaphtho[1,2-b]quinolizinium bromide with arylboronic acids. The resulting cationic biaryl derivatives exhibit pronounc...

Piperazine-2,3-dicarboxylic acid derivatives as dual antagonists of NMDA and GluK1-containing kainate receptors.

J. Med. Chem. 55(1) , 327-41, (2012)

Competitive N-methyl-d-aspartate receptor (NMDAR) antagonists bind to the GluN2 subunit, of which there are four types (GluN2A-D). We report that some N(1)-substituted derivatives of cis-piperazine-2,...

6-bromonaphthalene-2-carboxylic acid methyl ester

2-Naphthalenecarboxylic acid, 6-bromo-, methyl ester

Methyl 6-Bromo-2-naphthalenecarboxylate

methyl-6-bromonaphtoate

6-Bromo-2-naphthalenecarboxylic acid methyl ester

MFCD00100408

L66J CVO1 HE

Methyl 6-bromo-2-naphthoate

6-Bromo-2-naphthoic acid methyl ester