1975-51-5 Suppliers

Recommended suppliersmore

Product
FOB Price
Min.Order
Supply Ability
Supplier
Contact Supplier

2-Methyl-4-nitrobenzoic acid
Cas No: 1975-51-5
USD $ 3.0-3.0 / Kilogram
1 Kilogram
1-100 Metric Ton/Month
Dayang Chem (Hangzhou) Co.,Ltd.
Contact Supplier

High quality 2-Methyl-4-Nitrobenzoic Acid supplier in China
Cas No: 1975-51-5
No Data
No Data
Metric Ton/Day
Simagchem Corporation
Contact Supplier

2-Methyl-4-nitrobenzoic acid
Cas No: 1975-51-5
USD $ 10.0-10.0 / Gram
1 Gram
20 Metric Ton/Year
Jinan Finer Chemical Co., Ltd
Contact Supplier

2-Methyl-4-nitrobenzoic acid
Cas No: 1975-51-5
No Data
1 Kilogram
10 Metric Ton/Month
Henan Allgreen Chemical Co.,Ltd
Contact Supplier

Factory Supply 2-Methyl-4-Nitrobenzoic Acid
Cas No: 1975-51-5
No Data
1
1
Ality Chemical Corporation
Contact Supplier

2-Methyl-4-nitrobenzoic acid
Cas No: 1975-51-5
USD $ 5.0-5.0 / Kilogram
1 Kilogram
1000 Kilogram/Month
Enke Pharma-tech Co.,Ltd. （Cangzhou, China ）
Contact Supplier

2-Methyl-4-Nitrobenzoic Acid
Cas No: 1975-51-5
No Data
1 Metric Ton
1 million Metric Ton/Year
COLORCOM LTD.
Contact Supplier

4-Nitro-o-toluic acid (COOH=1)
Cas No: 1975-51-5
USD $ 1.2-5.0 / Kiloliter
5 Kiloliter
3000 Metric Ton/Month
Chemwill Asia Co., Ltd.
Contact Supplier

2-Methyl-4-nitrobenzoic acid 1975-51-5
Cas No: 1975-51-5
No Data
1 Kilogram
1 Metric Ton/Week
Henan Tianfu Chemical Co., Ltd.
Contact Supplier

2-Methyl-4-nitrobenzoic acid
Cas No: 1975-51-5
USD $ 2.0-10.0 / Kilogram
1 Kilogram
200 Metric Ton/Day
Hebei Nengqian Chemical Import and Export Co., LTD
Contact Supplier

1975-51-5 Usage

Uses

2-Methyl-4-nitrobenzoic acid is used as a reagent to synthesize amino-1H-pyrazole amide derivatives, compounds that act as Raf kinase inhibitors in melanoma cells. 2-Methyl-4-nitrobenzoic acid is also used as a reagent to synthesize fluorogenic substrates, compounds that can be used for activity imaging within living cells.

Check Digit Verification of cas no

The CAS Registry Mumber 1975-51-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1975-51:
(6*1)+(5*9)+(4*7)+(3*5)+(2*5)+(1*1)=105
105 % 10 = 5
So 1975-51-5 is a valid CAS Registry Number.

InChI:InChI=1/C8H7NO4/c1-5-4-6(9(12)13)2-3-7(5)8(10)11/h2-4H,1H3,(H,10,11)

1975-51-5 Well-known Company Product Price

Brand
(Code)Product description
CAS number
Packaging
Price
Detail

Alfa Aesar
(H31332) 2-Methyl-4-nitrobenzoic acid, 97%
1975-51-5
1g
592.0CNY
Detail

Alfa Aesar
(H31332) 2-Methyl-4-nitrobenzoic acid, 97%
1975-51-5
5g
1686.0CNY
Detail

1975-51-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-Methyl-4-nitrobenzoic acid

1.2 Other means of identification

Product number	-
Other names	2-Methyl-4-nitro-benzoesaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1975-51-5 SDS

1975-51-5Synthetic route

: 99-51-4
4-nitro-o-xylene

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With N-hydroxyphthalimide; cobalt(II) chloride hexahydrate; nitric acid; manganese (II) acetate tetrahydrate under 760.051 Torr; for 12h; Reagent/catalyst; Concentration; Reflux;	72%
With oxygen; sodium hydroxide In methanol; water at 65℃; under 13501.4 Torr; for 24h; Solvent; Temperature; Concentration; Autoclave;	62%
With oxygen; sodium hydroxide In ethanol; water at 60℃; under 7500.75 - 13501.4 Torr; for 24h; Solvent; Green chemistry; chemoselective reaction;	58%
With manganese(IV) oxide; nitric acid for 1h; Time;

: 99584-16-4
2-methyl-4-nitro-benzoic acid amide

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With hydrogenchloride In water for 20h; Heating / reflux;	89.5%
With hydrogenchloride for 20h; Hydrolysis; Heating;	88%
With sulfuric acid; sodium nitrite

: 89001-53-6
2-cyano-5-nitrotoluene

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With sodium hydroxide; dihydrogen peroxide In water Heating;	83%
With hydrogenchloride; acetic acid at 165℃;
With sodium hydroxide

palladium(II) dichloride bis(triphenylphosphine): palladium(II) dichloride bis(triphenylphosphine)

: 6277-17-4
2-iodo-3-nitrotoluene

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With potassium carbonate In diethyl ether; hexane; water; pyrographite; ethyl acetate; N,N-dimethyl-formamide
With potassium carbonate In diethyl ether; hexane; water; pyrographite; ethyl acetate; N,N-dimethyl-formamide
With potassium carbonate In diethyl ether; hexane; water; pyrographite; ethyl acetate; N,N-dimethyl-formamide

: 2-methyl-4-nitrobenzeneacetamide

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
Stage #1: 2-methyl-4-nitrobenzeneacetamide With sodium hypochlorite; potassium permanganate at 80℃; for 0.666667h; Stage #2: With hydrogenchloride for 2h; Temperature;

: 2486-75-1
4-amino-2-methylbenzoic acid

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With Streptomyces thioluteus para-aminobenzoate N-oxygenase

: 99-52-5
2-methyl-4-nitro-benzenamine

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: aq. HCl; NaNO2 / 0 - 5 °C 1.2: 81 percent / KCN / ethyl acetate / 20 °C 2.1: 98 percent / 80 percent aq. H2SO4 / 1.25 h / 100 °C 3.1: 88 percent / 6 N aq. HCl / 20 h / Heating View Scheme
Multi-step reaction with 3 steps 1.1: 1 h / 60 °C 1.2: 2 h / 60 °C 2.1: dihydrogen peroxide; sodium perborate / 2 h / 300 °C / 22502.3 Torr 2.2: 0.83 h / 70 °C 3.1: potassium permanganate; sodium hypochlorite / 0.67 h / 80 °C 3.2: 2 h View Scheme

1-<2-methyl-4-nitro-phenyl>-propane-1,2-dione-1-oxime: 1-<2-methyl-4-nitro-phenyl>-propane-1,2-dione-1-oxime

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With hydrogenchloride; sulfuric acid at 120℃;

: 108-88-3
toluene

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1.1: nitric acid; sulfuric acid / toluene / 1.25 h / 20 - 65 °C 2.1: tin(ll) chloride; iron; acetic acid / 0.5 h / 85 °C 2.2: 0.83 h 3.1: 1 h / 60 °C 3.2: 2 h / 60 °C 4.1: dihydrogen peroxide; sodium perborate / 2 h / 300 °C / 22502.3 Torr 4.2: 0.83 h / 70 °C 5.1: potassium permanganate; sodium hypochlorite / 0.67 h / 80 °C 5.2: 2 h View Scheme

: 22162-16-9
2-methyl-4-nitrobenzylpyridinium bromide

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
With sodium hydroxide; bromine

asymm. nitro-o-xylene: asymm. nitro-o-xylene

A: 1975-51-5
2-methyl-4-nitrobenzoic acid

B: 1975-52-6
5-nitro-o-toluic acid

Conditions

Conditions	Yield
With water; nitric acid
With nitric acid

: 619-15-8
2,5-dinitrotoluene

: 1975-51-5
2-methyl-4-nitrobenzoic acid

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1.1: tin(ll) chloride; iron; acetic acid / 0.5 h / 85 °C 1.2: 0.83 h 2.1: 1 h / 60 °C 2.2: 2 h / 60 °C 3.1: dihydrogen peroxide; sodium perborate / 2 h / 300 °C / 22502.3 Torr 3.2: 0.83 h / 70 °C 4.1: potassium permanganate; sodium hypochlorite / 0.67 h / 80 °C 4.2: 2 h View Scheme

: 99-51-4
4-nitro-o-xylene

: 7697-37-2
nitric acid

A: 1975-51-5
2-methyl-4-nitrobenzoic acid

B: 1975-52-6
5-nitro-o-toluic acid

: 7647-01-0
hydrogenchloride

: 89001-53-6
2-cyano-5-nitrotoluene

: 64-19-7
acetic acid

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 67-56-1
methanol

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 62621-09-4
methyl 2-methyl-4-nitrobenzoate

Conditions

Conditions	Yield
With thionyl chloride at 70℃; for 4h;	100%
With thionyl chloride at 70℃; for 18h;	100%
With thionyl chloride at 20℃; for 21h; Esterification;	99%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 74-88-4
methyl iodide

: 62621-09-4
methyl 2-methyl-4-nitrobenzoate

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h;	100%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 2h;	98%
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 3h;	89%
With potassium carbonate In N,N-dimethyl-formamide at 0 - 20℃; for 4h;

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 75-65-0
tert-butyl alcohol

: tert-butyl 4-amino-2-methylbenzoate

Conditions

Conditions	Yield
Stage #1: 2-methyl-4-nitrobenzoic acid; tert-butyl alcohol With pyridine; p-toluenesulfonyl chloride at 0 - 20℃; Stage #2: With hydrogen; palladium 10% on activated carbon In ethyl acetate at 20℃; for 2h;	100%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 2486-75-1
4-amino-2-methylbenzoic acid

Conditions

Conditions	Yield
With 5%-palladium/activated carbon; hydrogen In ethanol under 12001.2 Torr; Flow reactor;	98%
With hydrogenchloride; tin
With hydrogen; palladium 10% on activated carbon In methanol at 20℃; for 16h;

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 22162-15-8
(2-methyl-4-nitro-phenyl)methanol

Conditions

Conditions	Yield
With Trimethyl borate; dimethylsulfide borane complex In tetrahydrofuran at 65℃; for 2h; Inert atmosphere;	98%
With Trimethyl borate; dimethylsulfide borane complex In tetrahydrofuran for 6h; Reduction; Heating;	93%
With Trimethyl borate; dimethylsulfide borane complex In tetrahydrofuran Reflux;	90%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: (S)-dibenzyl 2-(2-ethoxy-4-(5-((((R)-2-((R)-1-(N-hydroxyformamido)propyl)heptanamido)methyl)carbamoyl)furan-2-yl)benzamido)succinate

: (S)-dibenzyl 2-(2-ethoxy-4-(5-((((R)-2-((R)-1-(N-((2-methyl-4-nitrobenzoyl)oxy)formamido)propyl)heptanamido)methyl)carbamoyl)furan-2-yl)benzamido)succinate

Conditions

Conditions	Yield
With 4-methyl-morpholine; HATU In N,N-dimethyl-formamide; acetonitrile at 50℃; for 16h;	98%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: C8H4F3NO4

Conditions

Conditions	Yield
With hydrogen fluoride; acetic acid; sodium nitrite In dichloromethane; water at 5 - 25℃; for 1h; Reagent/catalyst; Temperature;	95.8%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 41202-77-1
1-(2,3-dichlorophenyl)piperazine

: (4-(2,3-dichlorophenyl)piperazin-1-yl)(2-methyl-4-nitrophenyl)methanone

Conditions

Conditions	Yield
Stage #1: 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 0.333333h; Stage #2: 1-(2,3-dichlorophenyl)piperazine In N,N-dimethyl-formamide at 20℃;	95%

: 2971-79-1
isonipecotic acid methyl ester

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: methyl 1-(2-methyl-4-nitrobenzoyl)piperidine-4-carboxylate

Conditions

Conditions	Yield
Stage #1: isonipecotic acid methyl ester; 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: With HATU In dichloromethane for 0h; Inert atmosphere;	93.4%
Stage #1: isonipecotic acid methyl ester; 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.5h; Stage #2: With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane	93.4%
Stage #1: isonipecotic acid methyl ester; 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.5h; Inert atmosphere; Stage #2: With N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane for 10h; Inert atmosphere;	93.4%
Stage #1: isonipecotic acid methyl ester; 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.5h; Stage #2: With HATU In dichloromethane for 10h;	93.4%
Stage #1: isonipecotic acid methyl ester; 2-methyl-4-nitrobenzoic acid With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 0.5h; Stage #2: With HATU In dichloromethane for 10h;	93.4%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: (E)-2-hydroxy-1-(methyl(oxo)(phenyl)-λ6-sulfaneylidene)guanidine

: methyl((5-(2-methyl-4-nitrophenyl)-1,2,4-oxadiazol-3-yl)imino)(phenyl)-λ6-sulfanone

Conditions

Conditions	Yield
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In 2-methyltetrahydrofuran; ethyl acetate at 0 - 80℃; Inert atmosphere;	92%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 101084-64-4
2-methyl-4,5-dinitro-benzoic acid

Conditions

Conditions	Yield
With sulfuric acid; nitric acid	89%
With sulfuric acid; nitric acid at 0 - 20℃; for 16h; Inert atmosphere;	89%
With sulfuric acid; nitric acid at 0 - 20℃; for 120h;	85%

: 64-17-5
ethanol

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 62621-10-7
2-methyl-4-nitro-benzoic acid ethyl ester

Conditions

Conditions	Yield
With sulfuric acid for 24h; Heating / reflux;	82.99%
sulfuric acid Reflux;

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 93-55-0
1-phenyl-propan-1-one

: C17H15NO5

Conditions

Conditions	Yield
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; chloro(1,5-cyclooctadiene)rhodium(I) dimer; copper diacetate; cesium fluoride In toluene at 120℃; for 24h; Inert atmosphere;	72%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 99-08-1
1-methyl-3-nitrobenzene

Conditions

Conditions	Yield
With [Au(1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazol-2-ylidene)(O2CAd)] In toluene at 140℃; for 20h;	71%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 151297-83-5
4-amino-5-(naphthalen-1-yl-methyl)-3-mercapto-1,2,4-triazole

: 3-(1-naphthylmethyl)-6-(2-nitro-4-methylphenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole

Conditions

Conditions	Yield
With trichlorophosphate for 4h; Heating;	65%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 76457-90-4
4-amino-5-[4-(N,N-dimethylamino)phenyl]-3-mercapto-1,2,4-triazole

: 3-[4-(N,N-dimethylamino)phenyl]-6-(2-nitro-4-methylphenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole

Conditions

Conditions	Yield
With trichlorophosphate for 4h; Heating;	62%

: 914978-98-6
4-amino-5-[2-(N-methylamino)phenyl]-3-mercapto-1,2,4-triazole

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 3-[2-(N-methylamino)phenyl]-6-(2-nitro-4-methylphenyl)-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazole

Conditions

Conditions	Yield
With trichlorophosphate for 4h; Heating;	60%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 37156-27-7
2-(bromomethyl)-4-nitrobenzoic acid

Conditions

Conditions	Yield
With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) In tetrachloromethane at 80℃; for 16h;	59%

: 15233-97-3
Methylenbis(6-t-butyl-4-methyl-o-phenylen)hydrogenphosphit

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: C31H36NO6P

Conditions

Conditions	Yield
Stage #1: 2-methyl-4-nitrobenzoic acid With thionyl chloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 6h; Inert atmosphere; Stage #2: Methylenbis(6-t-butyl-4-methyl-o-phenylen)hydrogenphosphit With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 6h; Inert atmosphere;	55%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: tert-butyl methyl(3-(piperidine-4-carboxamido)propyl)carbamate

: tert-butyl methyl(3-(1-(2-methyl-4-nitrobenzoyl)piperidine-4-carboxamido)propyl)carbamate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 4h; Inert atmosphere;	47.16%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 4h;	47.16%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 4h;	47.16%
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 4h;	47.16%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 67081-02-1
5-nitro-3H-isobenzofuran-1-one

Conditions

Conditions	Yield
With sodium bromate; magnesium chloride In acetonitrile at 20℃; for 18h; Inert atmosphere; Irradiation; Sealed tube;	38%

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 30459-70-2
2-methyl-4-nitrobenzoyl chloride

Conditions

Conditions	Yield
With thionyl chloride
With thionyl chloride Heating;
With thionyl chloride Substitution;

: 1975-51-5
2-methyl-4-nitrobenzoic acid

: 623-33-6
glycine ethyl ester hydrochloride

: (2-Methyl-4-nitro-benzoylamino)-acetic acid ethyl ester

Conditions

Conditions	Yield
With 1,1'-carbonyldiimidazole 1) DMF, 0 deg C -> room temperature, 20 min, 2) DMF, room temperature, 30 min; Yield given. Multistep reaction;

1975-51-5Upstream product

1975-51-5Downstream Products

1975-51-5Relevant articles and documents

Oxidation of 4-nitro-o-xylene with nitric acid using N-hydroxyphthalimide under phase transfer conditions

Wei, Song-Bo,Tang, Bo,Peng, Xin-Hua

, p. 580 - 585 (2015)

4-Nitro-o-xylene was selectively oxidized to 2-methyl-4-nitrobenzoic acid using dilute nitric acid as the oxidizing agent under atmospheric pressure. The oxidation of 4-nitro-o-xylene was effectively promoted by an addition of radical initiators. Under re

Metal-Free Aerobic Oxidation of Nitro-Substituted Alkylarenes to Carboxylic Acids or Benzyl Alcohols Promoted by NaOH

Fang, Kun,Li, Guijie,She, Yuanbin

, p. 8092 - 8103 (2018/06/25)

Efficient and selective aerobic oxidation of nitro-substituted alkylarenes to functional compounds is a fundamental process that remains a challenge. Here, we report a metal-free, efficient, and practical approach for the direct and selective aerobic oxidation of nitro-substituted alkylarenes to carboxylic acids or benzyl alcohols. This sustainable system uses O2 as clean oxidant in a cheap and green NaOH/EtOH mixture. The position and type of substituent critically affect the products. In addition, this sustainable protocol enabled gram-scale preparation of carboxylic acid and benzyl alcohol derivatives with high chemoselectivities. Finally, the reactions can be conducted in a pressure reactor, which can conserve oxygen and prevent solvent loss. The approach was conducive to environmental protection and potential industrial application.

Method for synthesis of 2-aldehyde-4-aminobenzoic acid

-

Paragraph 0006, (2017/04/03)

The invention relates to a method for synthesis of 2-aldehyde-4-aminobenzoic acid. The method for synthesis of 2-aldehyde-4-aminobenzoic acid, which is provided by the invention, is simple and cheap, gentle in reaction condition in the preparation process, and high in yield.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 1975-51-5

CAS

1975-51-5

1975-51-5

Basic information

Chemical Properties

Safety Data

1975-51-5 Suppliers

Recommended suppliersmore

1975-51-5 Usage

Uses

Check Digit Verification of cas no

1975-51-5 Well-known Company Product Price

1975-51-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

1.Identification

1.1 GHS Product identifier

1.2 Other means of identification

1.3 Recommended use of the chemical and restrictions on use

1.4 Supplier's details

1.5 Emergency phone number

1975-51-5Synthetic route

1975-51-5Upstream product

1975-51-5Downstream Products

1975-51-5Relevant articles and documents

Oxidation of 4-nitro-o-xylene with nitric acid using N-hydroxyphthalimide under phase transfer conditions

Wei, Song-Bo,Tang, Bo,Peng, Xin-Hua

, p. 580 - 585 (2015)

Metal-Free Aerobic Oxidation of Nitro-Substituted Alkylarenes to Carboxylic Acids or Benzyl Alcohols Promoted by NaOH

Fang, Kun,Li, Guijie,She, Yuanbin

, p. 8092 - 8103 (2018/06/25)

Method for synthesis of 2-aldehyde-4-aminobenzoic acid

-

Paragraph 0006, (2017/04/03)