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10601-99-7

10601-99-7 Structure

10601-99-7 Structure
IdentificationBack Directory
[Name]

3-ETHYNYL-BENZOIC ACID
[CAS]

10601-99-7
[Synonyms]

3-ETHYNYL-BENZOIC ACID
3-Eethynylbenzoic acid
Benzoic acid, 3-ethynyl-
3-Ethynylbenzoic acid 95%
Benzoic acid, 3-ethynyl- (9CI)
3-ethynylbenzoic acid(SALTDATA: FREE)
[Molecular Formula]

C9H6O2
[MDL Number]

MFCD06658448
[MOL File]

10601-99-7.mol
[Molecular Weight]

146.14
Chemical PropertiesBack Directory
[Melting point ]

164-171°C
[Boiling point ]

300.2±25.0 °C(Predicted)
[density ]

1.23±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

powder
[pka]

3.99±0.10(Predicted)
[Appearance]

White to off-white Solid
[InChI]

1S/C9H6O2/c1-2-7-4-3-5-8(6-7)9(10)11/h1,3-6H,(H,10,11)
[InChIKey]

PHPIMLZTBYCDSX-UHFFFAOYSA-N
[SMILES]

OC(=O)c1cccc(c1)C#C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H317-H319
[Precautionary statements ]

P280-P301+P312+P330-P302+P352-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-36-43
[Safety Statements ]

26-36/37/39
[WGK Germany ]

nwg
[HS Code ]

2916399090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Irrit. 2
Skin Sens. 1
Spectrum DetailBack Directory
[Spectrum Detail]

3-ETHYNYL-BENZOIC ACID(10601-99-7)1HNMR
3-ETHYNYL-BENZOIC ACID(10601-99-7)FT-IR
Hazard InformationBack Directory
[Synthesis]

Methyl 3-((triMethylsilyl)ethynyl)benzoate

77123-59-2

3-ETHYNYL-BENZOIC ACID

10601-99-7

Step 2: Methyl 3-((trimethylsilyl)ethynyl)benzoate (105) (2.42 g) was dissolved in methanol (30 mL), and 2N aqueous sodium hydroxide solution (10.4 mL) was slowly added under cooling in an ice bath, and the reaction was stirred at room temperature for 7 hours. After completion of the reaction, the pH of the reaction mixture was adjusted to 3~4 with 2N hydrochloric acid, followed by concentration under reduced pressure. Water (100 mL) was added to the residue and extracted with ethyl acetate (100 mL). The organic layer was washed with saturated brine (100 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give 3-ethynylbenzoic acid (106) as a white solid (1.50 g, 99% yield).

[References]

[1] Journal of Medicinal Chemistry, 2012, vol. 55, # 22, p. 9562 - 9575
[2] Patent: JP5725475, 2015, B2. Location in patent: Paragraph 0028; 0031
[3] Patent: WO2014/168824, 2014, A1. Location in patent: Page/Page column 19
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