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98-50-0 Usage

Chemical Properties

p-Arsanilic acid is an off-white powder. It is slightly soluble in cold water. It is incompatible with oxidizing agents; on hazardous decomposition, p-arsanilic acid produces nitrogen oxides, carbon monoxide, carbon dioxide, nitrogen gas, and oxides of arsenic.

Originator

Arsanilic acid,Fleming Laboratories, Inc.

Uses

Different sources of media describe the Uses of 98-50-0 differently. You can refer to the following data:
1. 4-Aminophenylarsonic acid is an organoarsenic compound. 4-Aminophenylarsonic acid is a highly toxic contaminant and can be found in plants growing in contaminated soil. 4-Aminophenylarsonic acid was used as an additive in animal feed. It has also been used in treating dysentery in swine as well as having potential chemotherapeutic activity.
2. Arsanilic acid reacts essentially analogously to phenylarsonic acid. According to Chandelle, in the presence of relatively large amounts of accompanying ions the determination of zirconium gives more accurate results with this reagent than with phenylarsonic acid. This statement has not yet been confirmed. Nevertheless, the reagent is much more widely used than any other arsonic acid derivative.
3. manufacture of medicinal arsenicals.

Manufacturing Process

342.0 g (2 mol) of 83% arsenic acid were added during 75 min to a rapidly stirred mixture of 372.5 g (4 mol) aniline and 111.0 g chlorobenzene while the temperature of the mixture was kept at 147°-150°C. After the addition of arsenic acid was complete the mixture was stirred for an additional 8 h while being maintained at 149°-153°C. Water was continuously removed by distillation, and the organic phase of the distillate was continuously recycled back into the reaction mixture. At the end of that time a total of 121.0 g of water, containing the condensation of aniline and arsenic acid has been removed. The mixture was then allowed to cool to 110°C. 562.0 g (2.81 mol) of 20% sodium hydroxide were added over a 2 h period while water, chlorobenzene and excess aniline were distilled off at a temperature of from 102°-113°C. The distillation was continued for an additional 2 h while the volume of the mixture was kept at about 700 ml by the addition of water. The mixture was then diluted with water to a volume of 1400 ml and allowed to cool to 23°C. At this point, 52.0 g of by-product material, which was predominantly tri-(p-aminophenyl)-arsineoxide, were filtered out. The pH of the filtrate was then brought from 8.7 to 5.1 by the addition of 1.8 mol of hydrochloric acid while the volume of the mixture was increased to 2,200 ml by the addition of water. The mixture was stirred for 5 h at room temperature and again filtered. 108.0 g of by-product material comprising predominantly di-(p-aminophenyl)-arsinic acid was filtered off at this point. The pH of the filtrate was lowered to 4.5 by the addition of 0.2 mole of hydrochloric acid, and an additional 5.0 g of by-products, the composition of which was not determined, was filtered off. The filtrate was then brought to a pH of 3.2 by addition of 0.6 mole of hydrochloric acid, and 128.0 g (29.5% based upon arsenic acid) of arsanilic acid were recovered as a precipitate. The arsanilic acid filtrate was combined with the by-products filtered off during each of the three filtration steps. 2.8 mol of hydrochloric acid were added to the combined arsanilic acid filtrate and the mixture was heated at 80°C for 5 days. Arsanilic acid was then precipitated from the remaining hydrolyzed mixture in the manner described for the primary reaction product, and an additional 120.0 g (27.5% based on arsenic acid) were recovered. The filtrate contained 14.0 g (3.2%) of arsanilic acid which could be recovered at least partially in subsequent processing. Thus it can be seen from this example that an arsanilic acid yield of 59% was obtained.

Therapeutic Function

Antibacterial

Hazard

Toxic.

Health Hazard

Occupational workers exposed to p-arsanilic acid develop poisoning. The symptoms include, but are not limited to, eye and skin irritation, chemical conjunctivitis and corneal damage, hyperpigmentation of the skin and, perkeratoses of plantar and palmar surfaces, primary irritation and sensitization, digestive tract irritation, gastrointestinal hypermotility, diarrhea, hepatitis, hepatocellular necrosis, central nervous system depression, cardiac disturbances, and liver and kidney damage. The target organs include the kidneys, central nervous system, liver, and cardiovascular system. After a prolonged period of exposure to arsenic compounds, including arsenical dust, workers are known to develop shortness of breath, nausea, chest pains, garlic odor, and impairment of peripheral circulation. The toxicological properties of p-arsanilic acid have not been fully investigated.

Safety Profile

Poison by intravenous and intraperitoneal routes. Moderately toxic by ingestion. Flammable, decomposes with heat to yield flammable vapors. When heated to decomposition or on contact with acid or acid fumes it emits highly toxic fumes of As and NO,. See also ARSENIC COMPOUNDS and ANILINE.

storage

p-Arsanilic acid should be kept stored in a tightly closed container in a cool, dry, wellventilated area. It should be kept away from incompatible materials, dust generation, excess heat, and strong oxidants.

Purification Methods

Crystallise it from water or ethanol/ether. POISONOUS. [Beilstein 16 I 466.]

Precautions

Occupational workers should wash thoroughly after using p-arsanilic acid. Any contaminated clothing should be washed before reuse. Work areas should have adequate ventilation and minimum dust generation and accumulation. Workers should avoid any kind of contact of p-arsanilic acid with the eyes, skin, clothing, ingestion or inhalation.

Check Digit Verification of cas no

The CAS Registry Mumber 98-50-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 98-50:
(4*9)+(3*8)+(2*5)+(1*0)=70
70 % 10 = 0
So 98-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H8AsNO3/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H,8H2,(H2,9,10,11)

98-50-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B24595)  p-Arsanilic acid, 98%   

  • 98-50-0

  • 100g

  • 302.0CNY

  • Detail
  • Alfa Aesar

  • (B24595)  p-Arsanilic acid, 98%   

  • 98-50-0

  • 500g

  • 1185.0CNY

  • Detail
  • USP

  • (1042703)  Arsanilic acid  United States Pharmacopeia (USP) Reference Standard

  • 98-50-0

  • 1042703-25MG

  • 4,647.24CNY

  • Detail

98-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name arsanilic acid

1.2 Other means of identification

Product number -
Other names p-Arsanilic acid

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:98-50-0 SDS

98-50-0Synthetic route

nitarsone
98-72-6

nitarsone

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
With sodium hydroxide; hydrogen; palladium under 1520 - 2280 Torr;
With hydrogen; sodium acetate; palladium under 1520 - 2280 Torr;
With sodium hydroxide; iron(II) sulfate
With hydrogenchloride; iron at 85 - 90℃;
anilinium arsenate
63957-41-5

anilinium arsenate

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
at 190 - 200℃;
aniline
62-53-3

aniline

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
at 190 - 200℃; beim Erhitzen von arsensaurem Anilin;
orthoarsenic acid
7778-39-4, 121471-47-4

orthoarsenic acid

aniline
62-53-3

aniline

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

bis-(4-amino-phenyl)-arsinous acid
857587-34-9

bis-(4-amino-phenyl)-arsinous acid

Conditions
ConditionsYield
at 170 - 200℃;
aniline
62-53-3

aniline

arsenic acidic aniline

arsenic acidic aniline

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

bis-(4-amino-phenyl)-arsinous acid
857587-34-9

bis-(4-amino-phenyl)-arsinous acid

Conditions
ConditionsYield
at 180℃;
4.4'-diamino-arsenobenzene

4.4'-diamino-arsenobenzene

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
With dihydrogen peroxide
With iodine; acetic acid
orthoarsenic acid
7778-39-4, 121471-47-4

orthoarsenic acid

aniline
62-53-3

aniline

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
at 170 - 200℃;
arsenic acidic aniline

arsenic acidic aniline

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
at 190 - 200℃;
4-aminophenylarsenoxide
1122-90-3

4-aminophenylarsenoxide

iodine
7553-56-2

iodine

acetic acid
64-19-7

acetic acid

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

nitarsone
98-72-6

nitarsone

iron(II) sulfate

iron(II) sulfate

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

4-aminophenylarsenoxide
1122-90-3

4-aminophenylarsenoxide

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

alkali

alkali

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

nitarsone
98-72-6

nitarsone

sodium acetate
127-09-3

sodium acetate

hydrogen

hydrogen

palladium

palladium

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

nitarsone
98-72-6

nitarsone

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

hydrogen

hydrogen

palladium

palladium

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

carbarsone
121-59-5

carbarsone

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

ammonia
7664-41-7

ammonia

C

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

Conditions
ConditionsYield
Zers.;
N-(4-methoxy-benzoyl)-glycine-(4-arsono-anilide)
860728-63-8

N-(4-methoxy-benzoyl)-glycine-(4-arsono-anilide)

water
7732-18-5

water

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
Hydrolysis;
[(4-amino-phenyl)-arsanediyldimercapto]-di-acetic acid
31253-24-4

[(4-amino-phenyl)-arsanediyldimercapto]-di-acetic acid

air

air

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
beim Behandeln der alkal. Loesung;
N-(N-ethoxycarbonyl-glycyl)-glycine-(4-arsono-anilide)
857829-92-6

N-(N-ethoxycarbonyl-glycyl)-glycine-(4-arsono-anilide)

diluted NaOH-solution

diluted NaOH-solution

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
at 85 - 95℃;
orthoarsenic acid
7778-39-4, 121471-47-4

orthoarsenic acid

aniline
62-53-3

aniline

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

bis-(4-amino-phenyl)-arsinic acid
6309-25-7

bis-(4-amino-phenyl)-arsinic acid

Conditions
ConditionsYield
at 170 - 200℃;
In not given at 150°C;; only small amount of (NH2C6H4)2AsO(OH);;
In not given excess of aniline;;
In not given at 150°C;; only small amount of (NH2C6H4)2AsO(OH);;
In not given excess of aniline;;
aniline
62-53-3

aniline

arsenic acidic aniline

arsenic acidic aniline

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

bis-(4-amino-phenyl)-arsinic acid
6309-25-7

bis-(4-amino-phenyl)-arsinic acid

Conditions
ConditionsYield
at 180℃;
hydrogenchloride
7647-01-0

hydrogenchloride

bis-(4-amino-phenyl)-arsinic acid
6309-25-7

bis-(4-amino-phenyl)-arsinic acid

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

aniline
62-53-3

aniline

Conditions
ConditionsYield
at 100℃; untersucht wurde die Geschwindigkeit; verschiedener Konzentration.Hydrolysis;
at 130℃; untersucht wurde die Geschwindigkeit; verschiedener Konzentration.Hydrolysis;
p-nitrobenzenediazonium
14368-49-1

p-nitrobenzenediazonium

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: alkali; sodium arsenite
2: ferrosulfate; NaOH-solution
View Scheme
orthoarsenic acid
7778-39-4, 121471-47-4

orthoarsenic acid

aniline
62-53-3

aniline

A

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

B

C6H5NHAsO(OH)2

C6H5NHAsO(OH)2

Conditions
ConditionsYield
In not given heating to 190°C;;A n/a
B 0%
In not given
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

p-aminophenyldichloroarsine. hydrochloride
5410-78-6

p-aminophenyldichloroarsine. hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; sulfur dioxide; potassium iodide In methanol at 20℃; for 0.75h;98%
With hydrogenchloride; sulfur dioxide; potassium iodide In methanol; water for 0.5h;95%
With hydrogenchloride; sulfur dioxide; potassium iodide In methanol; water at 0℃; for 0.5h;93.7%
With hydrogenchloride; sulfur dioxide; potassium iodide In methanol; water at 20℃; for 0.5h;
With hydrogenchloride; sulfur dioxide; potassium iodide In methanol; water
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2-Bromoacetyl bromide
598-21-0

2-Bromoacetyl bromide

4-(N-(bromoacetyl)amino)phenylarsonic acid
51146-91-9

4-(N-(bromoacetyl)amino)phenylarsonic acid

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With sodium carbonate In water at 4℃; for 2h;
Stage #2: 2-Bromoacetyl bromide In dichloromethane; water at 0 - 20℃; for 0.6h;
Stage #3: With sulfuric acid; water pH=4;
95%
With sodium carbonate; potassium hydroxide In dichloromethane; water for 0.25h; Cooling with ice;71.4%
With sodium carbonate In water at 0 - 20℃; for 1.16667h;
With sodium carbonate In water at 0 - 20℃; for 1h; Cooling with ice;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

(4-azidophenyl)arsonic acid

(4-azidophenyl)arsonic acid

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With hydrogenchloride In water at 0℃; for 0.166667h;
Stage #2: With sodium nitrite In water at 0℃; for 0.25h;
Stage #3: With sodium azide In water at 0 - 20℃; for 12h;
94%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

Methacryloyl chloride
920-46-7

Methacryloyl chloride

p-methacroloylaminophenylarsonic acid

p-methacroloylaminophenylarsonic acid

Conditions
ConditionsYield
In ethanol at 4℃; for 2h;93%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

3-Bromopropionyl chloride
15486-96-1

3-Bromopropionyl chloride

4-(bromopropionamido)-phenylarsanilic acid
636576-17-5

4-(bromopropionamido)-phenylarsanilic acid

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With potassium hydroxide; sodium hydrogencarbonate In water
Stage #2: 3-Bromopropionyl chloride In water at 0℃; for 0.116667h;
Stage #3: With sulfuric acid In water at 0℃; pH=1;
89%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2-chloropropionyl chloride
625-36-5

2-chloropropionyl chloride

(4-(3-chloropropanamido)phenyl)arsonic acid
74175-13-6

(4-(3-chloropropanamido)phenyl)arsonic acid

Conditions
ConditionsYield
With sodium carbonate; potassium hydroxide In dichloromethane; water Cooling with ice;87.58%
Stage #1: p-aminophenylarsonic acid With sodium carbonate; potassium hydroxide In water Cooling with ice;
Stage #2: 2-chloropropionyl chloride In dichloromethane; water for 0.333333h; Cooling with ice;
87.58%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

undec-10-enoyl chloride
38460-95-6

undec-10-enoyl chloride

C17H26AsNO4

C17H26AsNO4

Conditions
ConditionsYield
In ethanol for 4h; Cooling with ice;87%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

6,7-dimethoxy-4-chloroquinazoline
13790-39-1

6,7-dimethoxy-4-chloroquinazoline

4-(4'-phenylarsonic acid)amino-6,7-dimethoxyquinazoline

4-(4'-phenylarsonic acid)amino-6,7-dimethoxyquinazoline

Conditions
ConditionsYield
With hydrogenchloride In isopropyl alcohol Heating;85.4%
for 24h; Heating;
With hydrogenchloride In isopropyl alcohol Heating;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

water
7732-18-5

water

copper(II) acetate monohydrate
6046-93-1

copper(II) acetate monohydrate

molybdenum(VI) oxide

molybdenum(VI) oxide

[{Cu(2,2'-bipyridine)(H2O)}2Mo6O18(O3AsC6H4NH2)2]·3H2O

[{Cu(2,2'-bipyridine)(H2O)}2Mo6O18(O3AsC6H4NH2)2]·3H2O

Conditions
ConditionsYield
With ammonium fluoride at 135℃; for 48h; pH=3 - 4; Autoclave;85%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

4-Chloro-2-methylthiopyrimidine
49844-90-8

4-Chloro-2-methylthiopyrimidine

2-methylthio-4-(4'-aminophenylarsonic acid)aminopyrimidine

2-methylthio-4-(4'-aminophenylarsonic acid)aminopyrimidine

Conditions
ConditionsYield
With hydrogenchloride In isopropyl alcohol Heating;82.5%
for 24h; Heating;
With hydrogenchloride In isopropyl alcohol Heating;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

sodium metavanadate

sodium metavanadate

water
7732-18-5

water

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

Na5[V5O9(4-aminohenylarsonate)4]*20.5H2O*3DMF

Na5[V5O9(4-aminohenylarsonate)4]*20.5H2O*3DMF

Conditions
ConditionsYield
With NaN3; N2H4*H2O; HCl In water; N,N-dimethyl-formamide mixt. of NaVO3, NaN3, acid, H2O and DMF was stirred at 70°C untilclear soln. formed; N2H4*H2O, concd. aq. HCl were added at 70°C to pH 7.3; stirred for 15 min; filtered; cooled to room temp.; filtered after 1 d; kept for 2 d;82%
1.3-propanedithiol
109-80-8

1.3-propanedithiol

p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2-(4-aminophenyl)-1,3,2-dithiarsinane

2-(4-aminophenyl)-1,3,2-dithiarsinane

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate In ethanol at 55℃; for 1h;
Stage #2: 1.3-propanedithiol In ethanol for 0.5h;
80%
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate at 50℃; for 2h;
Stage #2: 1.3-propanedithiol
52%
Stage #1: p-aminophenylarsonic acid With ammonium thioglycolate at 50℃; for 2h;
Stage #2: 1.3-propanedithiol
52%
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate at 50℃; for 0.5h;
Stage #2: 1.3-propanedithiol
35%
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate at 50℃; for 0.5h;
Stage #2: 1.3-propanedithiol
35%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

cobalt(II) diacetate tetrahydrate
6147-53-1

cobalt(II) diacetate tetrahydrate

molybdenum(VI) oxide

molybdenum(VI) oxide

[{Co(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

[{Co(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

Conditions
ConditionsYield
With ammonium fluoride In water at 135℃; for 48h; pH=4; Autoclave;75%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

allyl bromide
106-95-6

allyl bromide

C12H16AsNO3

C12H16AsNO3

Conditions
ConditionsYield
With tetrabutylammomium bromide; sodium carbonate In dichloromethane; water at 20℃; for 65h;75%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

6-chloropurine
87-42-3

6-chloropurine

6-(4'-phenylarsonic acid)aminopurine
17053-73-5

6-(4'-phenylarsonic acid)aminopurine

Conditions
ConditionsYield
With hydrogenchloride In isopropyl alcohol Heating;71.3%
for 24h; Heating;
With hydrogenchloride In isopropyl alcohol Heating;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

dihydrolipoic acid
462-20-4

dihydrolipoic acid

2-aminophenyl-4-pentanoic-1,3,2-dithiaarsinane

2-aminophenyl-4-pentanoic-1,3,2-dithiaarsinane

Conditions
ConditionsYield
In methanol for 24h;71%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

lead(II) nitrate

lead(II) nitrate

[Pb(4-aminophenylarsonic acid)(NO3)2]

[Pb(4-aminophenylarsonic acid)(NO3)2]

Conditions
ConditionsYield
In water at 100℃; for 1h;71%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

N,N-dimethyl-2,3-dihydroxybenzamide
70656-94-9

N,N-dimethyl-2,3-dihydroxybenzamide

bis(2,3,7,8,b,h)-(1NN-dimethylamidobenzo)-5-arsa-5-paraaminophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane
141033-38-7, 141116-18-9, 185951-12-6

bis(2,3,7,8,b,h)-(1NN-dimethylamidobenzo)-5-arsa-5-paraaminophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane

Conditions
ConditionsYield
In benzene for 48h; Heating;70%
In acetic anhydride for 0.333333h; Heating;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

N,N-Diethyl-2,3-dihydroxy-benzamide
141033-37-6

N,N-Diethyl-2,3-dihydroxy-benzamide

bis(2,3,7,8,b,h)-(1NN-diethylamidobenzo)-5-arsa-5-paraaminophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane
141033-42-3, 141116-22-5, 185951-32-0

bis(2,3,7,8,b,h)-(1NN-diethylamidobenzo)-5-arsa-5-paraaminophenyl 1,4,6,9-tetraoxaspiro(4,4)nonane

Conditions
ConditionsYield
In benzene for 48h; Heating;70%
In acetic anhydride for 0.333333h; Heating;
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

succimer
304-55-2

succimer

2-(4-aminophenyl)-1,3,2-dithiaarsolane-4,5-dicarboxylic acid

2-(4-aminophenyl)-1,3,2-dithiaarsolane-4,5-dicarboxylic acid

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate In ethanol at 55℃; for 1h;
Stage #2: succimer In ethanol for 0.5h;
68%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

phenol
108-95-2

phenol

4-(4'-hydroxyphenylazo)phenylarsonic acid
5425-66-1

4-(4'-hydroxyphenylazo)phenylarsonic acid

Conditions
ConditionsYield
62%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

zinc(II) acetate dihydrate
5970-45-6

zinc(II) acetate dihydrate

molybdenum(VI) oxide

molybdenum(VI) oxide

[{Zn(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

[{Zn(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

Conditions
ConditionsYield
With ammonium fluoride In water at 135℃; for 48h; pH=4; Autoclave;60%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

ethane-1,2-dithiol
540-63-6

ethane-1,2-dithiol

4-(1,3,2-dithiocycloarsenic-2-yl)aniline
5577-20-8

4-(1,3,2-dithiocycloarsenic-2-yl)aniline

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate In ethanol at 55℃; for 1h;
Stage #2: ethane-1,2-dithiol In ethanol for 0.5h;
60%
Stage #1: p-aminophenylarsonic acid With phenylhydrazine In methanol Reflux;
Stage #2: ethane-1,2-dithiol In ethanol for 0.333333h; Reflux;
34%
Stage #1: p-aminophenylarsonic acid With phenylhydrazine In methanol for 1.5h; Reflux;
Stage #2: ethane-1,2-dithiol In ethanol for 0.333333h; Reflux;
1.8 g
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2,3-dimercaptopropanol
59-52-9

2,3-dimercaptopropanol

(2-(4-aminophenyl)-1,3,2-dithiarsolan-4-yl)methanol

(2-(4-aminophenyl)-1,3,2-dithiarsolan-4-yl)methanol

Conditions
ConditionsYield
Stage #1: p-aminophenylarsonic acid With ammonium 2-sulfanylacetate at 50℃; for 0.5h;
Stage #2: 2,3-dimercaptopropanol
58%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

2,2':6,2''-terpyridine
1148-79-4

2,2':6,2''-terpyridine

[Cu2(OAc)4(H2O)2]
879089-16-4, 155065-88-6

[Cu2(OAc)4(H2O)2]

water
7732-18-5

water

molybdenum(VI) oxide

molybdenum(VI) oxide

[(Cu(2,2':6',6''-terpyridine))2Mo4O13H(AsO4)]*2H2O

[(Cu(2,2':6',6''-terpyridine))2Mo4O13H(AsO4)]*2H2O

Conditions
ConditionsYield
With H2SO4 In water High Pressure; mixt. of MoO3, Cu acetate, terpyridine, p-arsanilic acid, H2O (mole ratio = 2.51:1.00:1.00:1.25:1253) and concd. H2SO4 stirred briefly, heated at 150°C for 48 h under autogenous pressure; crystals isolated;55%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

silver trifluoromethanesulfonate
2923-28-6

silver trifluoromethanesulfonate

[Ag(4-aminophenylarsonic acid(-1H))(4-aminophenylarsonic acid)]

[Ag(4-aminophenylarsonic acid(-1H))(4-aminophenylarsonic acid)]

Conditions
ConditionsYield
With potassium hydroxide In ethanol; water at 100℃; for 1h;55%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

ammonium heptamolybdate tetrahydrate

ammonium heptamolybdate tetrahydrate

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

2NH4(1+)*2H(1+)*(Mo4O8(NH2C6H4AsO3)4)(4-)*HCON(CH3)2*4H2O=(NH4)2H2(Mo4O8(NH2C6H4AsO3)4)*HCON(CH3)2*4H2O

2NH4(1+)*2H(1+)*(Mo4O8(NH2C6H4AsO3)4)(4-)*HCON(CH3)2*4H2O=(NH4)2H2(Mo4O8(NH2C6H4AsO3)4)*HCON(CH3)2*4H2O

Conditions
ConditionsYield
With ammonium acetate; N2H4*H2SO4; acetic acid In water; N,N-dimethyl-formamide to soln. (NH4)6Mo7O24*4H2O and AcONH4 in water-DMF at room temp. N2H4*H2SO4 was added, stirred for 5 min, p-arsanic acid was added, stirred for 10 min, pH was adjusted to 4.9 with aq. AcOH, kept for 5-7 days; elem. anal.;53%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

(4-aminophenyl)arsenous acid

(4-aminophenyl)arsenous acid

Conditions
ConditionsYield
With phenylhydrazine In methanol for 1h; Reflux;53%
With phenylhydrazine In methanol for 1h; Reflux;53%
With phenylhydrazine for 2.5h; Reflux;40%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

n-dodecanoyl chloride
112-16-3

n-dodecanoyl chloride

C18H30AsNO4

C18H30AsNO4

Conditions
ConditionsYield
In ethanol for 4h; Cooling with ice;51%
p-aminophenylarsonic acid
98-50-0

p-aminophenylarsonic acid

[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

nickel(II) acetate tetrahydrate
6018-89-9

nickel(II) acetate tetrahydrate

molybdenum(VI) oxide

molybdenum(VI) oxide

[{Ni(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

[{Ni(2,2′-bipyridine)2}2Mo6O18(O3AsC6H4NH2)2]

Conditions
ConditionsYield
With ammonium fluoride In water at 135℃; for 48h; pH=4; Autoclave;50%

98-50-0Relevant articles and documents

Cheetham,Schmidt

, p. 828 (1920)

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