Methyl 6-bromo-2-naphthoate Basic information |
Product Name: | Methyl 6-bromo-2-naphthoate |
Synonyms: | 6-Bromo-2-Naphtoic Acid Methyl Ester;2-Bromo-6-naphthoic acid methylester;6-BROMO-2-NAPHTHALENECARBOXYLIC ACID METHYL ESTER;6-BROMO-2-NAPHTHOIC ACID METHYL ESTER;METHYL 6-BROMO-2-NAPHTHALENECARBOXYLATE;METHYL 6-BROMO-2-NAPHTHOATE;2-Naphthoic acid, 6-bromo, methyl ester;Methyl-6-bromo-2-naphtoate |
CAS: | 33626-98-1 |
MF: | C12H9BrO2 |
MW: | 265.1 |
EINECS: | 608-896-0 |
Product Categories: | Naphthalene series;Building Blocks;C12 to C63;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Aromatic Esters;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Intermediates of Adapalene;C12 to C63;Carbonyl Compounds;Esters;API;Others chemical reagents;blocks;Bromides;Carboxes;ADAPALENE |
Mol File: | 33626-98-1.mol |
Methyl 6-bromo-2-naphthoate Chemical Properties |
Melting point | 123-126 °C (lit.) |
Boiling point | 357.0±15.0 °C(Predicted) |
density | 1.492±0.06 g/cm3(Predicted) |
storage temp. | Sealed in dry,Room Temperature |
solubility | Chloroform (Slightly), DMSO (Slightly) |
form | Crystalline Powder |
color | Off-white to cream or light brown |
BRN | 2578943 |
InChIKey | JEUBRLPXJZOGPX-UHFFFAOYSA-N |
CAS DataBase Reference | 33626-98-1(CAS DataBase Reference) |
Safety Information |
Hazard Codes | C |
Risk Statements | 20/21/22-34 |
Safety Statements | 24/25-45-36/37/39-27-26 |
WGK Germany | 3 |
HS Code | 29163990 |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
ACROS | English |
ALFA | English |
Methyl 6-bromo-2-naphthoate Usage And Synthesis |
Chemical Properties | Pale yellow or light brown powder |
Uses | Methyl 6-Bromo-2-napthoate is used in the synthesis of Adapalene, a retinoid specific for RARβ and RARγ receptors. |
Uses | Methyl 6-Bromo-2-napthoate (Adapalene USP Related Compound A) is used in the synthesis of Adapalene, a retinoid specific for RARβ and RARγ receptors. |
Uses | Methyl 6-bromo-2-naphthoate may be used to synthesize:
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General Description | Methyl 6-bromo-2-naphthoate undergoes aromatic Finkelstein reaction followed by hydrolysis to afford 6-iodo-2-naphthoic acid. |
Methyl 6-bromo-2-naphthoate Preparation Products And Raw materials |
Preparation Products | 2,2'-Bis-(1-adaMantyl)-4,4'-diMethoxybiphenyl-->2-Acetyl-6-bromonaphthalene |
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