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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene

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Company Name: Jinan Chenghui Shuangda biological Co., LTD  Gold
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Company Name: Jiangsu Vcare PharmaTech Co., Ltd.  Gold
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Company Name: CHENGHUI PHARMACEUTICAL GROUP LTD  Gold
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Company Name: Gansu HaoTian Chemical Technology Co., Ltd.  Gold
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4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Basic information
Product Name:4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene
Synonyms:Dapagliflozin Intermediate 1;4-broMo-1-chloro-2-[(4-ethoxyphenyl)Methyl]-;2-(4-Methoxybenzyl)-4-broMo-1-chlorobenzene;Dapagliflozin-13;Dapagliflozin Bromo impurity;5-broMo-2-chloro-4’Dapagliflozin Intermediate II;Dapagliflozin Intermediate 2
CAS:461432-23-5
MF:C15H14BrClO
MW:325.63
EINECS:636-921-5
Product Categories:Halides;Phenyls & Phenyl-Het;461432-23-5;ADVANCED INT.
Mol File:461432-23-5.mol
4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Structure
4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Chemical Properties
Boiling point 393.0±32.0 °C(Predicted)
density 1.371±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly)
form Low-Melting Solid
color White to Off-White
Stability:Stable under recommended storage conditions., Stable Under Recommended Storage C
InChIInChI=1S/C15H14BrClO/c1-2-18-14-6-3-11(4-7-14)9-12-10-13(16)5-8-15(12)17/h3-8,10H,2,9H2,1H3
InChIKeyZUNCHZBITMUSRD-UHFFFAOYSA-N
SMILESC1(Cl)=CC=C(Br)C=C1CC1=CC=C(OCC)C=C1
Safety Information
HS Code 2909309090
MSDS Information
4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Usage And Synthesis
Uses5-Bromo-2-chloro-4'-ethoxydiphenylmethane is a hydrocarbon derivative and can be used as an intermediate for dapagliflozin.
SynthesisOxalyl chloride (0.8 mL) was added to a solution of 5-bromo-2-chlorobenzoic acid (2 g) in dichloromethane (20 mL) and dimethylformamide (0.2 mL) under a nitrogen atmosphere. The reaction mixture was stirred for one hour at 25° C to 30° C. After completion of the reaction, the reaction mixture was concentrated under a vacuum at 40° C to 45° C. to obtain an oily residue. The oily residue was dissolved in dichloromethane (20 mL) and cooled to 0° C. To this solution, phenol (1.1 mL) and aluminium chloride (2.3 g) were added at 0° C. to 5° C. The reaction mixture was stirred at 0° C to 5° C for 2 hours. The reaction mixture was allowed to warm to about 20° C, and triethylsilane (3.4 mL) was slowly added to it at the same temperature. The reaction mixture was stirred for about 36 hours from 20° C to 25° C. After completion of the reaction, 4-bromo-1-chloro-2-(4-ethoxybenzyl)benzene was obtained by further purification.
4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene Preparation Products And Raw materials
Preparation Products(2S,3R,4S,5S)-2-(4-chloro-3-(4-ethoxybenzyl)phenyl)-6,6-bis(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol-->Bexagliflozin-->4-(5-broMo-2-chlorobenzyl)phenol
Tag:4-Bromo-1-chloro-2-(4-ethoxybenzyl)benzene(461432-23-5) Related Product Information
2-(5-BroMo-2-Methylbenzyl)-5-(4-fluorophenyl)thiophene (R)-3-(4-(5-broMo-2-chlorobenzyl)phenoxy)tetrahydrofuran 2,3,4,6-Tetrakis-O-trimethylsilyl-D-gluconolactone 4-(5-broMo-2-chlorobenzyl)phenol 2,3,4,6-Tetra-O-pivaloyl-alpha-D-glucopyranosyl bromide 2-(4-Fluorophenyl)-5-[(5-iodo-2-methylphenyl)methyl]thiophene Empagliflozin Canagliflozin heMihydrate PF-04971729 Ipragliflozin Canagliflozin Donepezil 1-Chloro-2-(4-ethoxybenzyl)-4-iodobenzene 5-Bromo-2-chlorobenzoic acid (5-broMo-2-chlorophenyl)(2-ethoxyphenyl)Methanone (5-bromo-2-chlorophenyl)(4-ethoxyphenyl)methanone 4-Bromo-1-chloro-2-ethylbenzene 5-bromo-2-chloro-4’-ethoxydiphenylmethane