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2042-14-0

2042-14-0 Structure

2042-14-0 Structure
IdentificationMore
[Name]

4-Methyl-3-nitrophenol
[CAS]

2042-14-0
[Synonyms]

3-NITRO-4-METHYLPHENOL
3-NITRO-P-CRESOL
4-HYDROXY-1-METHYL-2-NITROBENZENE
4-HYDROXY-2-NITROTOLUENE
4-METHYL-3-NITROPHENOL
NITRO-4-CRESOL
TIMTEC-BB SBB008513
2-Nitro-4-hydroxytoluene
3-Nitro-p-cresol(4-Methyl-3-nitrophenol)
p-Cresol, 3-nitro-
Phenol, 4-methyl-3-nitro-
Nitropcresol
4-Hydroxy-2-nitrotoluene 97%
4-METHYL-3-NITROPHENOL/3-NITRO-P-CRESOL
3-Nitro-p-cresol (OH=1)
4-METHYL-3-NITROPHENOL 98%
4-Methyl-5-nitrophenol
[EINECS(EC#)]

218-044-6
[Molecular Formula]

C7H7NO3
[MDL Number]

MFCD00007244
[Molecular Weight]

153.14
[MOL File]

2042-14-0.mol
Chemical PropertiesBack Directory
[Appearance]

Pale Yellow Crystalline Solid
[Melting point ]

78-81 °C (lit.)
[Boiling point ]

266.03°C (rough estimate)
[density ]

1.2744 (estimate)
[vapor pressure ]

0.084Pa at 25℃
[refractive index ]

1.5744 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Ethyl Acetate, Methanol
[form ]

Powder
[pka]

8.66±0.10(Predicted)
[color ]

Pale Yellow Crystalline
[Water Solubility ]

Slightly soluble in water.
[Cosmetics Ingredients Functions]

HAIR DYEING
[InChI]

InChI=1S/C7H7NO3/c1-5-2-3-6(9)4-7(5)8(10)11/h2-4,9H,1H3
[InChIKey]

BQEXDUKMTVYBRK-UHFFFAOYSA-N
[SMILES]

C1(O)=CC=C(C)C([N+]([O-])=O)=C1
[LogP]

2.18 at 25℃
[CAS DataBase Reference]

2042-14-0(CAS DataBase Reference)
[NIST Chemistry Reference]

4-Methyl-3-nitrophenol(2042-14-0)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[RIDADR ]

2446
[WGK Germany ]

3
[Hazard Note ]

Irritant
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29089990
[Storage Class]

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

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Raw materials And Preparation ProductsBack Directory
[Raw materials]

4-Methyl-3-nitroaniline-->Sodium nitrite-->Sulfuric acid
[Preparation Products]

6-Methoxy-1H-indole-3-carboxylic acid-->6-Hydroxyindole-->6-Methoxy-1H-indole-3-carbaldehyde-->6-Methoxyindole-->6-Benzyloxyindole-->5-Methoxy-2-methylaniline-->4-Methyl-3-nitroanisole-->4-Benzyloxy-2-nitrotoluene-->Benzenamine, 5-(difluoromethoxy)-2-methyl--->Diethyl azodicarboxylate
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

4-Methyl-3-nitrophenol(2042-14-0).msds
Hazard InformationBack Directory
[Chemical Properties]

Pale Yellow Crystalline Solid
[Uses]

3-Nitro-4-methylphenol (cas# 2042-14-0) is a compound useful in organic synthesis.
[Synthesis Reference(s)]

Synthesis, p. 735, 1986 DOI: 10.1055/s-1986-31759
[Synthesis]

4-Methyl-3-nitroaniline

119-32-4

4-Methyl-3-nitrophenol

2042-14-0

General procedure for the synthesis of 4-methyl-3-nitrophenol from 4-methyl-3-nitroaniline: 4-methyl-3-nitroaniline (200 mg, 1.31 mmol) was dissolved in a 3:1 mixture of H2SO4-H2O. The resulting mixture was heated to 100 °C and kept for 30 min. Upon completion of the reaction, the reaction mixture was cooled to 0 °C and NaNO2 solution was added slowly and dropwise. After the dropwise addition was completed, the reaction was continued for 1 hour, after which the mixture was heated to reflux. After the reaction was complete, the reaction mixture was extracted several times with EtOAc, the organic phases were combined and dried with anhydrous Na2SO4, and subsequently concentrated. The crude product was purified by fast column chromatography (eluent ratio: petroleum ether-ethyl acetate 9:1) to give a yellow solid in 70% yield. The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.48 (s, 1H), 7.17 (d, J = 8.4 Hz, 1H), 7.01 (dd, J = 8.4, 2.4 Hz, 1H), 5.84 (s, 1H), 2.48 (s, 3H) ppm.

[References]

[1] Chemistry - A European Journal, 2009, vol. 15, # 12, p. 2742 - 2746
[2] Patent: WO2016/128541, 2016, A1. Location in patent: Page/Page column 92; 93
[3] Patent: WO2017/162834, 2017, A1. Location in patent: Page/Page column 85
[4] Justus Liebigs Annalen der Chemie, 1882, vol. 215, p. 83
[5] Chemische Berichte, 1882, vol. 15, p. 2992
Spectrum DetailBack Directory
[Spectrum Detail]

4-Methyl-3-nitrophenol(2042-14-0)MS
4-Methyl-3-nitrophenol(2042-14-0)1HNMR
4-Methyl-3-nitrophenol(2042-14-0)13CNMR
4-Methyl-3-nitrophenol(2042-14-0)IR1
4-Methyl-3-nitrophenol(2042-14-0)IR2
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-Methyl-3-nitrophenol, 98%(2042-14-0)
[Alfa Aesar]

4-Methyl-3-nitrophenol, 98%(2042-14-0)
[Sigma Aldrich]

2042-14-0(sigmaaldrich)
[TCI AMERICA]

3-Nitro-p-cresol,>98.0%(T)(2042-14-0)
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