ChemicalBook--->CAS DataBase List--->18179-39-0

18179-39-0

18179-39-0 Structure

18179-39-0 Structure
IdentificationBack Directory
[Name]

METHYL 4-IODOSALICYLATE
[CAS]

18179-39-0
[Synonyms]

Methyl4-Iodosilicylate
Methyl4-Iodosalicylate>
Methyl 4-iodosalicylate 97%
4-Iodosalicylic Acid Methyl Ester
2-Hydroxy-4-iodobenzoic Acid Methyl Ester
Benzoic acid, 2-hydroxy-4-iodo-, methyl ester
Methyl 4-iodosalicylate, 5-Iodo-2-(methoxycarbonyl)phenol
Methyl 2-Hydroxy-4-iodobenzoate 4-Iodosalicylic Acid Methyl Ester 2-Hydroxy-4-iodobenzoic Acid Methyl Ester
[Molecular Formula]

C7H7IO2Si
[MDL Number]

MFCD06797864
[MOL File]

18179-39-0.mol
[Molecular Weight]

278.119
Chemical PropertiesBack Directory
[Melting point ]

69-73 °C
[Boiling point ]

309.7±32.0 °C(Predicted)
[density ]

1.880±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

powder to crystal
[pka]

8.91±0.10(Predicted)
[color ]

White to Gray to Brown
[Sensitive ]

Light Sensitive
[InChI]

1S/C8H7IO3/c1-12-8(11)6-3-2-5(9)4-7(6)10/h2-4,10H,1H3
[InChIKey]

WUFUURSWOJROKY-UHFFFAOYSA-N
[SMILES]

COC(=O)c1ccc(I)cc1O
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
[F ]

8
[Hazard Note ]

Toxic
[PackingGroup ]

III
[HS Code ]

2918290090
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Questions And AnswerBack Directory
[Structure]

2-hy­droxy-4-iodo­benzoic acid methyl ester (methyl 4-iodo­salicylate, C8H7IO3) allows for an effective way of incorporating the methyl salicylates within larger organic mol­ecules, using such methodologies as McClure protocols, which take advantage of the iodine atom at the 4-position of the aromatic ring for the formation of carbon-carbon bonds. The iodine atom is also capable of forming supra­molecular synthons, which may be useful for crystal engineering. At 90 K, the methyl 4-iodo­salicylat displays monoclinic (P21/c) symmetry with one mol­ecule in the asymmetric unit. Inter­molecular hydrogen bonding inter­actions occur between the hy­droxy groups of one mol­ecule and the carbonyl oxygen atom of the methyl ester of an adjacent mol­ecule to form a centrosymmetric dimeric pair with H⋯O = 2.53 (4) Å. An O3—H3⋯O2 intra­molecular hydrogen bond also exists with an H⋯O distance of 2.05 (4) Å. The C5⋯C8 [3.326 (3) Å] and O3⋯H1C (2.51 Å) inter­actions provide only short contacts between the stacks of offset (102) parallel sheets, which make up the crystal. These sheets, in turn, contain the inversion-generated hydrogen-bonded dimers. The non-hydrogen atoms of the mol­ecule are essentially coplanar with no displacement from the mean mol­ecular plane greater than 0.132 Å.
METHYL 4-IODOSALICYLATE
[Application]

4-Iodosalicylic acid methyl ester is an ester organic compound that can be used as a chemical reagent.
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl 4-iodosalicylate(18179-39-0)1HNMR
Methyl 4-iodosalicylate(18179-39-0)FT-IR
Hazard InformationBack Directory
[Synthesis]

2-HYDROXY-4-IODOBENZOIC ACID

16870-28-3

Iodomethane

74-88-4

Methyl 4-iodosalicylate

18179-39-0

General procedure for the synthesis of methyl 4-iodosalicylate from 2-hydroxy-4-iodobenzoic acid and iodomethane: 4-iodosalicylic acid (7.3 g, 27.65 mmol) was dissolved in 41 mL of DMF, NaHCO3 (2.78 g, 33.18 mmol) was added, and CO2 was released during the reaction and the mixture was stirred for 5 min. Iodomethane (2.66 mL, 5.85 g, 41.47 mmol, 1.5 eq.) was then added and the reaction mixture was heated with stirring at 40 °C for 5 h (the reaction progress was monitored by TLC). After completion of the reaction, the mixture was diluted with 170 mL of water and 170 mL of ethyl acetate (EA). The organic layer was washed sequentially with 170 mL of 5% NaHCO3 solution and 170 mL of 5% NaCl solution and dried with Na2SO4. Evaporation of the solvent gave about 9 g of crude product (in the form of a black oil), which was purified by column chromatography: 100 g of silica gel (SiO2) was used as stationary phase, and the eluent was pure hexane, which was subsequently adjusted to a solvent mixture of hexane:ethyl acetate (100:2). Finally, 5.86 g of pure product was obtained in 76.5% yield.

[References]

[1] Patent: US2016/2269, 2016, A1. Location in patent: Paragraph 0253; 0254
18179-39-0 suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Alfa Aesar  
Telephone: 400-6106006
Website: http://chemicals.thermofisher.cn
Company Name: TCI (Shanghai) Development Co., Ltd.  
Telephone: 021-67121386
Website: https://www.tcichemicals.com/CN/zh/
Company Name: Energy Chemical  
Telephone: 400-0056266
Website: www.energy-chemical.com
Company Name: Accela ChemBio Co.,Ltd.  
Telephone: 021-50795510 4000665055
Website: http://www.shao-yuan.com/
Company Name: Shanghai Longsheng chemical Co.,Ltd.  
Telephone: 58099637 13585536065
Website: www.shlshg.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Telephone: 021-54306202 13764082696
Website: https://www.hanhongsci.com
Company Name: Shandong Xiya Chemical Co., Ltd  
Telephone: 13355009207 13355009207
Website: http://www.xiyashiji.com
Company Name: Shanghai Sunway Pharmaceutical Technology Co., Ltd  
Telephone: 13761987713
Website: www.sunwaypharm.cn
Company Name: ZhengZhou HuaWen Chemical Co.Ltd  
Telephone: 0370-2785118 17550508557
Website: http://www.hnhwchem.com
Company Name: 9ding chemical ( Shanghai) Limited  
Telephone: 4009209199
Website: www.9dingchem.com
Company Name: Shanghai Aladdin Bio-Chem Technology Co.,LTD  
Telephone: 400-6206333 13167063860
Website: www.aladdin-e.com/
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Finetech Industry Limited  
Telephone: 027-87465837 19945049750
Website: https://www.finetechchem.com/
Company Name: Sigma-Aldrich  
Telephone: 021-61415566 800-8193336
Website: https://www.sigmaaldrich.cn
Company Name: Zhengzhou Gecko Scientific Inc.  
Telephone: 0371-63336364 17344886665
Website: http://www.zzgecko.cn
Company Name: Changzhou Anxuan Chemical, Co., Ltd.  
Telephone: 13912302692
Website: http://www.anxuanchem.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Telephone: 15026964105
Website: www.shyuanye.com
Tags:18179-39-0 Related Product Information
119-36-8