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ChemicalBook >> CAS DataBase List >>METHYL 4-HYDROXY-3-IODOBENZOATE

METHYL 4-HYDROXY-3-IODOBENZOATE

CAS No.
15126-06-4
Chemical Name:
METHYL 4-HYDROXY-3-IODOBENZOATE
Synonyms
4-hydroxy-3-iodobenzoate;Methyl 3-Iodo-4-hydroxybenzoate;METHYL 4-HYDROXY-3-IODOBENZOATE;2-Iodo-4-(methoxycarbonyl)phenol;4-Methyl-4-Hydroxy-3-Iodobenzoate;Methyl 4-hydroxy-3-iodobenzoate 97%;Methyl 4-hydroxy-3-iodobenzoate, 98%,;4-HYDROXY-3-IODOBENZOIC ACID METHYL ESTER;Benzoic acid, 4-hydroxy-3-iodo-, methyl ester
CBNumber:
CB7335363
Molecular Formula:
C8H7IO3
Molecular Weight:
278.04
MDL Number:
MFCD05664378
MOL File:
15126-06-4.mol
MSDS File:
SDS
Last updated:2026-05-28 05:12:48
Product description Number Pack Size Price
Methyl 4-hydroxy-3-iodobenzoate 97% 631949 5g $84.2
Methyl 4-hydroxy-3-iodobenzoate FM41915 100g $150
Methyl 4-hydroxy-3-iodobenzoate FM41915 250g $195
Methyl 4-hydroxy-3-iodobenzoate FM41915 500g $355
Methyl 4-hydroxy-3-iodobenzoate FM41915 1000g $650
More product size

METHYL 4-HYDROXY-3-IODOBENZOATE Properties

Melting point 155-159 °C (lit.)
Boiling point 292.7±25.0 °C(Predicted)
Density 1.880±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka 6.91±0.18(Predicted)
form Crystal or Powder
color White to pale brown
Sensitive Light Sensitive
InChI InChI=1S/C8H7IO3/c1-12-8(11)5-2-3-7(10)6(9)4-5/h2-4,10H,1H3
InChIKey PXNOLLHARLSLHY-UHFFFAOYSA-N
SMILES C(OC)(=O)C1=CC=C(O)C(I)=C1
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H318
Precautionary statements  P280-P305+P351+P338-P264-P280i-P301+P312a-P310a-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  22-41
Safety Statements  26-39
WGK Germany  3
HS Code  2918290090
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Eye Dam. 1

METHYL 4-HYDROXY-3-IODOBENZOATE price More Price(42)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 631949 Methyl 4-hydroxy-3-iodobenzoate 97% 15126-06-4 5g $84.2 2023-06-20 Buy
Biosynth FM41915 Methyl 4-hydroxy-3-iodobenzoate 15126-06-4 100g $150 2026-06-04 Buy
Biosynth FM41915 Methyl 4-hydroxy-3-iodobenzoate 15126-06-4 250g $195 2026-06-04 Buy
Biosynth FM41915 Methyl 4-hydroxy-3-iodobenzoate 15126-06-4 500g $355 2026-06-04 Buy
Biosynth FM41915 Methyl 4-hydroxy-3-iodobenzoate 15126-06-4 1000g $650 2026-06-04 Buy
Product number Packaging Price Buy
631949 5g $84.2 Buy
FM41915 100g $150 Buy
FM41915 250g $195 Buy
FM41915 500g $355 Buy
FM41915 1000g $650 Buy

METHYL 4-HYDROXY-3-IODOBENZOATE Chemical Properties,Uses,Production

Chemical Properties

Off White Powder

Synthesis

Methylparaben

99-76-3

METHYL 4-HYDROXY-3-IODOBENZOATE

15126-06-4

GENERAL STEPS: Methyl 4-hydroxybenzoate (35.5 g, 0.233 mol) was dissolved in 200 mL of acetic acid, stirred and heated to 65°C. A solution of ICI (37.8 g, 0.233 mol) dissolved in 50 mL of acetic acid was added slowly and dropwise over 40 minutes. The reaction mixture was stirred at 65°C for 5 hours, followed by 16 hours at room temperature. The precipitated product was collected by filtration, washed with water and dried under vacuum to give 27.5 g of the target product (99% purity by LCMS and HNMR). The mother liquor was concentrated and the residue was washed with water and dried under vacuum to give an additional 31 g of the target product (95% purity analyzed by LCMS and HNMR).The total yield of methyl 4-hydroxy-3-iodobenzoate was 58.5 g in 90.3% yield.LCMS m/z 278. Synthesis of methyl 3-cyano-4-hydroxybenzoate 3: Methyl 4-hydroxy-3-iodobenzoate 2 (28 g, 0.1 mol) was dissolved in 100 mL of DMF and CuCN (9.92 g, 0.11 mol) and NaCN (0.49 g, 0.11 mol) were added. After the system was displaced with nitrogen, it was heated to 105 °C and stirred for 18 hours. It was cooled to room temperature, filtered to remove the precipitate and the filter cake was washed with EtOAc. The combined organic phases were diluted with 200 mL of water and extracted with EtOAc (2 x 200 mL). The combined organic layers were dried with sodium sulfate, filtered and concentrated to dryness. Vacuum drying gave 18 g (100% yield) of product 3, which was characterized by LCMS and HNMR. Synthesis of methyl 3-cyano-4-isopropoxybenzoate 4: Methyl 3-cyano-4-hydroxybenzoate 3 (18 g, 0.11 mol) was dissolved in 100 mL of DMF and 2-bromopropane (14.2 mL, 0.15 mol) and anhydrous potassium carbonate (41.9 g, 0.3 mol) were added. After the system was displaced with nitrogen, it was heated to 90 °C and stirred overnight. Cooled to room temperature, the reaction mixture was diluted with 200 mL of water and extracted with CH2Cl2 (2 x 200 mL). The organic layers were combined, dried with sodium sulfate, filtered and concentrated to dryness to give 20.5 g (99% yield) of the oily product 4, which was characterized by LCMS and HNMR. Synthesis of perfluorophenyl 3-cyano-4-isopropoxybenzoate 6: Methyl 3-cyano-4-isopropoxybenzoate 4 (20.5 g, 0.093 mol) was dissolved in 200 mL of a mixed methanol-water solvent of 6:4, NaOH (5.61 g, 0.14 mol) was added, and stirred for 2 h at room temperature. The solution was filtered through a silica gel plug and the solvent was removed under vacuum. The solid was redissolved in 200 mL of CH2Cl2 and perfluorophenyl 2,α,2-trifluoroacetate 5 (19.3 mL, 0.11 mol) and triethylamine (19.5 mL, 0.14 mol) were added. After standing overnight, the solution was filtered and the solid was washed with CH2Cl2. The combined organic phases were purified on a short silica gel column and concentrated to dryness to give 29 g (83.5% yield) of product 6, which was characterized by LCMS and HNMR.

References

[1] Patent: WO2005/107762, 2005, A2. Location in patent: Page/Page column 253-254
[2] Asian Journal of Chemistry, 2011, vol. 23, # 1, p. 41 - 43
[3] Patent: WO2005/40157, 2005, A2. Location in patent: Page/Page column 59-60
[4] Patent: WO2014/63199, 2014, A1. Location in patent: Page/Page column 74
[5] European Journal of Organic Chemistry, 2017, vol. 2017, # 22, p. 3234 - 3239

99-76-3
15126-06-4
Synthesis of METHYL 4-HYDROXY-3-IODOBENZOATE from Methylparaben
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View Lastest Price from METHYL 4-HYDROXY-3-IODOBENZOATE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
METHYL 4-HYDROXY-3-IODOBENZOATE pictures 2026-06-30 METHYL 4-HYDROXY-3-IODOBENZOATE
15126-06-4
1kg 98% 1000kg Shaanxi Dideu New Materials Co. Ltd
4-Hydroxy-3-iodo-benzoic acid methyl ester pictures 2024-04-02 4-Hydroxy-3-iodo-benzoic acid methyl ester
15126-06-4
$820.00 1g 98 500 Kg R&D Scientific Inc.
METHYL 4-HYDROXY-3-IODOBENZOATE pictures 2019-07-10 METHYL 4-HYDROXY-3-IODOBENZOATE
15126-06-4
$1.00 1KG 98% 150KG Career Henan Chemical Co

METHYL 4-HYDROXY-3-IODOBENZOATE Spectrum

METHYL 4-HYDROXY-3-IODOBENZOATE 4-HYDROXY-3-IODOBENZOIC ACID METHYL ESTER Methyl 3-Iodo-4-hydroxybenzoate 2-Iodo-4-(methoxycarbonyl)phenol Methyl 4-hydroxy-3-iodobenzoate 97% 4-hydroxy-3-iodobenzoate Benzoic acid, 4-hydroxy-3-iodo-, methyl ester Methyl 4-hydroxy-3-iodobenzoate, 98%, 4-Methyl-4-Hydroxy-3-Iodobenzoate 15126-06-4 Building Blocks Carbonyl Compounds C8 to C9 Organic Building Blocks Esters C8 to C9 Carbonyl Compounds Esters
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