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methyl 3-hydroxy-5-nitro-benzoate

Product Name
methyl 3-hydroxy-5-nitro-benzoate
CAS No.
55076-32-9
Chemical Name
methyl 3-hydroxy-5-nitro-benzoate
Synonyms
methyl 3-hydroxy-5-nitro-benzoate;3-hydroxy-5-nitrobenzoic acid, methyl ester;Benzoic acid, 3-hydroxy-5-nitro-, methyl ester
CBNumber
CB21259737
Molecular Formula
C8H7NO5
Formula Weight
197.14
MOL File
55076-32-9.mol
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methyl 3-hydroxy-5-nitro-benzoate Property

Melting point:
154-156 °C
Boiling point:
377.2±27.0 °C(Predicted)
Density 
1.432±0.06 g/cm3(Predicted)
pka
7.52±0.10(Predicted)
form 
powder
color 
Light yellow
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Safety

HS Code 
2918290090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
M320115
Product name
Methyl3-Hydroxy-5-nitrobenzoate
Packaging
250mg
Price
$125
Updated
2021/12/16
TRC
Product number
M320115
Product name
Methyl3-Hydroxy-5-nitrobenzoate
Packaging
500mg
Price
$195
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0152041
Product name
METHYL 3-HYDROXY-5-NITROBENZOATE
Purity
95.00%
Packaging
5MG
Price
$500.98
Updated
2021/12/16
AK Scientific
Product number
8016AB
Product name
Methyl3-hydroxy-5-nitrobenzoate
Packaging
10g
Price
$844
Updated
2021/12/16
Crysdot
Product number
CD12061944
Product name
Methyl3-hydroxy-5-nitrobenzoate
Purity
95+%
Packaging
10g
Price
$660
Updated
2021/12/16
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methyl 3-hydroxy-5-nitro-benzoate Chemical Properties,Usage,Production

Uses

Methyl 3-hydroxy-5-nitrobenzoate is a derivative of benzoic acid (B203900). Methyl 3-hydroxy-5-nitrobenzoate is used in synthetic preparations.

Synthesis

67-56-1

78238-14-9

55076-32-9

1. 3-Hydroxy-5-nitrobenzoic acid (3.7 g, 20.00 mmol) was dissolved in methanol (70.0 mL) at 0 °C. 2. Thionyl chloride (12.0 mL) was slowly added to the above solution. 3. The temperature of the reaction mixture was raised to 6 °C and stirred continuously for 3 hours. 4. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure. 5. Water was added to the residue and subsequently extracted with ethyl acetate. 6. The organic phases were combined, washed with saturated brine and dried over anhydrous sodium sulfate. 7. After filtration, the organic phase was concentrated under reduced pressure to afford the crude product methyl 3-hydroxy-5-nitrobenzoate (3.9 g) as an off-white solid which did not require further purification. 8. The structure of the product was determined by 1H-1H-beta-hydroxy-5-nitrobenzoic acid. 8. The structure of the product was confirmed by 1H-NMR (300 MHz, DMSO-d6): δ 10.96 (s, 1H), 8.08 (m, 1H), 7.78 (m, 1H), 7.70 (m, 1H), 3.90 (s, 3H).

References

[1] Journal of Medicinal Chemistry, 2016, vol. 59, # 10, p. 4812 - 4830
[2] Patent: US2014/350007, 2014, A1. Location in patent: Paragraph 0076; 0077; 0078
[3] Journal of Medicinal Chemistry, 1984, vol. 27, # 12, p. 1549 - 1559
[4] Patent: US2010/69431, 2010, A1. Location in patent: Page/Page column 110-111
[5] Patent: WO2014/196793, 2014, A1. Location in patent: Page/Page column 74

methyl 3-hydroxy-5-nitro-benzoate Preparation Products And Raw materials

Raw materials

Preparation Products

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methyl 3-hydroxy-5-nitro-benzoate Suppliers

FCH Group
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Email
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Ukraine
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