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3-Amino-N-phenylbenzenesulfonamide Chemical and Physical Properties

Names and Identifiers

- 3-Amino-N-phenylbenzenesulfonamide
- m-AMINOBENZENESULFONANILIDE
- 3-AMINOBENZENESULFONANILIDE
- 3-amino-n-phenyl-benzenesulfonamid
- m-aminobenzenesulphonanilide
- 3-Aminobenzene sulfanilide
- 3-Aminosulfonanilide
- Metanilanilide
- m-aminobenzensulfonanilid
- A839866
- BBL003796
- SR-01000326064
- DS-0496
- Benzenesulfonamide, 3-amino-N-phenyl-
- AKOS000143468
- 80-21-7
- UNII-TB92UA8FRX
- STK522202
- SMR000274072
- Z239126054
- TB92UA8FRX
- Benzenesulfonanilide, 3-amino-
- MLS000703707
- DTXSID7058830
- m-Aminobenzenesufhonanilide
- AM20060863
- m-Aminobenzene sulfonanilide
- SCHEMBL3973555
- SR-01000326064-1
- 3-amino-N-phenylbenzene-1-sulfonamide
- EN300-39177
- MFCD00035928
- W-104243
- NSC4989
- AC-11897
- CS-0207123
- FT-0689282
- 3-Amino-N-phenyl-benzenesulfonamide
- EINECS 201-259-4
- Benzenesulfonamide,3-amino-N-phenyl-
- CHEMBL1447534
- NSC-4989
- NSC 4989
- SOZFVONLAQIHRF-UHFFFAOYSA-N
- NCGC00245017-01
- NS00038066
- SY112648
- 3-Amino-N-phenylbenzenesulfonamide (ACI)
- Metanilanilide (6CI, 7CI, 8CI)
- 3-(N-Phenylaminosulfonyl)aniline
- ALBB-025720
- DB-014243
- MDL： MFCD00035928
- Inchi： 1S/C12H12N2O2S/c13-10-5-4-8-12(9-10)17(15,16)14-11-6-2-1-3-7-11/h1-9,14H,13H2
- InChI Key： SOZFVONLAQIHRF-UHFFFAOYSA-N
- SMILES： O=S(C1C=C(N)C=CC=1)(NC1C=CC=CC=1)=O

Computed Properties

Exact Mass: 248.06200
Monoisotopic Mass: 248.062
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 2
Hydrogen Bond Acceptor Count: 4
Heavy Atom Count: 17
Rotatable Bond Count: 3
Complexity: 331
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Topological Polar Surface Area: 80.6A^2
Surface Charge: 0
Tautomer Count: nothing
XLogP3: nothing

Experimental Properties

Color/Form: IV or Y powder
Density: 1.373
Melting Point: ≥121°C
Boiling Point: 458.9°C at 760 mmHg
Flash Point: 231.3 °C
Refractive Index: 1.669
PSA: 80.57000
LogP: 3.80460

3-Amino-N-phenylbenzenesulfonamide Security Information

Signal Word：Warning
Hazard Statement： H302-H315-H319-H332-H335
Warning Statement： P261-P280-P305+P351+P338
Storage Condition：Keep in dark place,Sealed in dry,2-8°C(BD22675)

3-Amino-N-phenylbenzenesulfonamide Customs Data

HS CODE：2935009090
Customs Data：

China Customs Code:
2935009090

Overview:

2935009090 Other sulphonates(Acyl)amine. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:35.0%

Declaration elements:

Product Name, component content, use to

Summary:

2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

3-Amino-N-phenylbenzenesulfonamide Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
Fluorochem	076733-1g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	95%	1g	￡25.00	2022-03-01
Fluorochem	076733-5g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	95%	5g	￡53.00	2022-03-01
Fluorochem	076733-25g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	95%	25g	￡158.00	2022-03-01
Fluorochem	076733-100g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	95%	100g	￡394.00	2022-03-01
Alichem	A019088487-25g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	97%	25g	$265.00	2023-09-01
Alichem	A019088487-100g	3-Amino-N-phenylbenzenesulfonamide	80-21-7	97%	100g	$353.50	2023-09-01
TRC	A061005-250mg	3-Amino-N-phenylbenzenesulfonamide	80-21-7		250mg	$ 185.00	2022-05-31
TRC	A061005-500mg	3-Amino-N-phenylbenzenesulfonamide	80-21-7		500mg	$ 300.00	2022-05-31
TRC	A061005-1000mg	3-Amino-N-phenylbenzenesulfonamide	80-21-7		1g	$ 480.00	2022-05-31
eNovation Chemicals LLC	D960367-5g	3-Aminobenzenesulfonanilide	80-21-7	97%	5g	$210	2024-06-06

3-Amino-N-phenylbenzenesulfonamide Production Method

Production Method 1

85169-25-1

80-21-7

Reaction Conditions

1.1 Reagents: Hydrochloric acid Solvents: Water ; rt → 100 °C; 2 h, 100 °C

Reference

Structure-activity relationships of agonists for the orphan G protein-coupled receptor GPR27

Pillaiyar, Thanigaimalai ; et al, European Journal of Medicinal Chemistry, 2021, 225,

Production Method 2

80-21-7

Reaction Conditions

1.1 Reagents: Chlorosulfonic acid ; 6 h, 150 °C
2.1 Reagents: Pyridine ; 1 h, 80 °C
3.1 Reagents: Iron , Ammonium chloride Solvents: Ethanol ; 2 h, 90 °C

Reference

Optimization of Potent and Specific Trypanothione Reductase Inhibitors: A Structure-Based Drug Discovery Approach

Battista, Theo; et al, ACS Infectious Diseases, 2022, 8(8), 1687-1699

Production Method 3

28791-26-6

80-21-7

Reaction Conditions

1.1 Reagents: Iron , Ammonium chloride Solvents: Ethanol ; 2 h, 90 °C

Reference

Optimization of Potent and Specific Trypanothione Reductase Inhibitors: A Structure-Based Drug Discovery Approach

Battista, Theo; et al, ACS Infectious Diseases, 2022, 8(8), 1687-1699

Production Method 4

28791-26-6

80-21-7

Reaction Conditions

1.1 Reagents: Iron , Ferrous sulfate Solvents: Methanol , Water ; overnight, reflux

Reference

Synthesis and anticandidal activity of azole-containing sulfonamides

Qandil, Amjad M.; et al, Archiv der Pharmazie (Weinheim, 2008, 341(2), 99-112

Production Method 5

98-80-6

98-18-0

80-21-7

Reaction Conditions

1.1 Reagents: Sodium hydride Catalysts: Cuprous chloride Solvents: Methanol ; 48 h, rt

Reference

Chemoselective N-arylation of aminobenzene sulfonamides via copper catalysed Chan-Evans-Lam reactions

Zu, Weisai; et al, Organic Chemistry Frontiers, 2019, 6(9), 1356-1360

Production Method 6

80-21-7

Reaction Conditions

1.1 Reagents: Pyridine ; 1 h, 80 °C
2.1 Reagents: Iron , Ammonium chloride Solvents: Ethanol ; 2 h, 90 °C

Reference

Optimization of Potent and Specific Trypanothione Reductase Inhibitors: A Structure-Based Drug Discovery Approach

Battista, Theo; et al, ACS Infectious Diseases, 2022, 8(8), 1687-1699

Production Method 7

23905-46-6

80-21-7

Reaction Conditions

1.1 Reagents: Triethylamine Solvents: Dichloromethane ; 0 °C; 2 h, rt
2.1 Reagents: Hydrochloric acid Solvents: Water ; rt → 100 °C; 2 h, 100 °C

Reference

Structure-activity relationships of agonists for the orphan G protein-coupled receptor GPR27

Pillaiyar, Thanigaimalai ; et al, European Journal of Medicinal Chemistry, 2021, 225,

Production Method 8

80-21-7

Reaction Conditions

1.1 Reagents: Chlorosulfonic acid
2.1 Solvents: Water
3.1 Reagents: Iron , Hydrochloric acid Solvents: Water

Reference

Synthesis of 3-methyl-1-phenyl-5-pyrazolones containing arylaminosulfonyl groups

Lisitsyn, V. N.; et al, Zhurnal Organicheskoi Khimii, 1994, 30(5), 735-9

3-Amino-N-phenylbenzenesulfonamide Raw materials

3-Amino-N-phenylbenzenesulfonamide Preparation Products

3-Amino-N-phenylbenzenesulfonamide (80-21-7)

3-Amino-N-phenylbenzenesulfonamide Suppliers

Amadis Chemical Company Limited

Gold Member

Audited Supplier

(CAS:80-21-7)3-Amino-N-phenylbenzenesulfonamide

Order Number:A839866

Stock Status:in Stock

Quantity:25g/100g

Purity:99%

Pricing Information Last Updated:Friday, 30 August 2024 06:47

Price ($):158.0/356.0

Email:[email protected]

Product Official Link

3-Amino-N-phenylbenzenesulfonamide Related Literature

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3. Distributed research: a new paradigm for undergraduate research and global problem solving?

Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511
4. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–

Chem. Commun., 1998, 1501-1502
5. Distribution characteristics of nitrogen and the related microbial community in the surface sediments of the Songhua River?

Congyu Li,Wenfu Wang,Haiyan Wang,Guokai Yan,Weiyang Dong,Zhaosheng Chu,Huan Wang,Yang Chang RSC Adv., 2021,11, 26721-26731

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Cas no 80-21-7 (3-Amino-N-phenylbenzenesulfonamide)

3-Amino-N-phenylbenzenesulfonamide Chemical and Physical Properties

Names and Identifiers

Computed Properties

Experimental Properties

3-Amino-N-phenylbenzenesulfonamide Security Information

3-Amino-N-phenylbenzenesulfonamide Customs Data

China Customs Code:

Overview:

Declaration elements:

Summary:

3-Amino-N-phenylbenzenesulfonamide Pricemore >>

3-Amino-N-phenylbenzenesulfonamide Production Method

Production Method 1

Production Method 2

Production Method 3

Production Method 4

Production Method 5

Production Method 6

Production Method 7

Production Method 8

3-Amino-N-phenylbenzenesulfonamide Raw materials

3-Amino-N-phenylbenzenesulfonamide Preparation Products

3-Amino-N-phenylbenzenesulfonamide Suppliers

3-Amino-N-phenylbenzenesulfonamide Related Literature

Related Categories

80-21-7 (3-Amino-N-phenylbenzenesulfonamide) Related Products