ChemicalBook > CAS DataBase List > 2,6-difluoro-4-methylbenzoic acid

2,6-difluoro-4-methylbenzoic acid

Product Name
2,6-difluoro-4-methylbenzoic acid
CAS No.
1201597-23-0
Chemical Name
2,6-difluoro-4-methylbenzoic acid
Synonyms
2,6-difluoro-4-methylbenzoic acid;Benzoic acid, 2,6-difluoro-4-methyl-;2,6-Difluoro-4-methylbenzoic acid 98%
CBNumber
CB31557540
Molecular Formula
C8H6F2O2
Formula Weight
172.13
MOL File
1201597-23-0.mol
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2,6-difluoro-4-methylbenzoic acid Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
White to yellow Solid
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Safety

HS Code 
2916399090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

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N-Bromosuccinimide Price

ChemScene
Product number
CS-W021528
Product name
2,6-Difluoro-4-methylbenzoicacid
Packaging
100mg
Price
$53
Updated
2021/12/16
Apolloscientific
Product number
PC56022
Product name
2,6-Difluoro-4-methylbenzoic acid
Purity
98%
Packaging
250mg
Price
$164
Updated
2021/12/16
SynQuest Laboratories
Product number
2721-3-2P
Product name
2,6-Difluoro-4-methylbenzoic acid
Packaging
250mg
Price
$194
Updated
2021/12/16
Apolloscientific
Product number
PC56022
Product name
2,6-Difluoro-4-methylbenzoic acid
Purity
98%
Packaging
1g
Price
$410
Updated
2021/12/16
AK Scientific
Product number
Z3965
Product name
2,6-Difluoro-4-methylbenzoicacid
Packaging
1g
Price
$471
Updated
2021/12/16
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2,6-difluoro-4-methylbenzoic acid Chemical Properties,Usage,Production

Synthesis

1201597-22-9

1201597-23-0

Step C: Synthesis of 2,6-difluoro-4-methylbenzoic acid 1. silver oxide (43.8 g, 0.189 mol), water (200 mL) and sodium hydroxide (33.7 g, 0.842 mol) were added to a flask. 2. 2,6-difluoro-4-methylbenzaldehyde (29.23 g, 0.187 mol) was added in batches over 30 min. 3. intense exothermic phenomena were observed during the reaction and the color of the reaction mixture changed from black to gray. 4. The thick suspension formed was continued to be stirred for 1 hour and subsequently filtered through a Brinell funnel. 5. The filtrate was acidified to pH 2 with concentrated hydrochloric acid to produce a suspension. 6. The precipitate was collected by filtration, dissolved in ether and dried by adding anhydrous sodium sulfate. 7. The dried solution was filtered and concentrated to give a white solid product, 2,6-difluoro-4-methylbenzoic acid (17.0 g, 53% yield). 8. The product was purified by 1H-NHPA and concentrated. 8. The product was characterized by 1H-NMR (500 MHz, d6-DMSO): δ 13.7 (br.s, 1H), 7.02 (d, 2H, J = 9.3 Hz), 2.32 (s, 3H).

References

[1] Patent: WO2010/129208, 2010, A1. Location in patent: Page/Page column 32-33
[2] Patent: WO2009/152072, 2009, A1. Location in patent: Page/Page column 35

2,6-difluoro-4-methylbenzoic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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1201597-23-0, 2,6-difluoro-4-methylbenzoic acidRelated Search:


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