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632-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 632-24-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 632-24:
(5*6)+(4*3)+(3*2)+(2*2)+(1*4)=56
56 % 10 = 6
So 632-24-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4S/c8-13(11,12)6-4-2-1-3-5(6)7(9)10/h1-4H,(H,9,10)(H2,8,11,12)

632-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzoic acid, o-sulfamoyl-

1.2 Other means of identification

Product number -
Other names 2-Carboxybenzenesulfonamide

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:632-24-6 SDS

632-24-6Synthetic route

N-(fluoromethyl)saccharin
133742-01-5

N-(fluoromethyl)saccharin

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
With sodium hydroxide In tetrahydrofuran59%
methyl 2-(aminosulfonyl)benzoate
88-19-7

methyl 2-(aminosulfonyl)benzoate

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
With potassium hydroxide; water; potassium hexacyanoferrate(III)
With alkaline manganate man reduziert ueberschuessiges Manganat mit Alkohol, macht die alkal.Fluessigkeit durch Saeurezusatz nahezu neutral, filtriert von MnO2 ab, dampft stark ein, saeuert an und extrahiert mit Aether;
With alkaline permanganate at 50 - 70℃; Erhitzen unter Druck auf 160grad;
Multi-step reaction with 2 steps
1: permanganate; water / in neutral gehaltenem Medium
2: NaOH-solution
View Scheme
saccharin
81-07-2

saccharin

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
With potassium hydroxide
With sodium hydroxide
With sodium hydroxide; water man dampft ein, bis der suesse Saccharingeschmack verschwunden ist, filtriert nach dem Erkalten, scheidet aus der Loesung durch Salzsaeurezusatz die o-Sulfamid-benzoesaeure aus und krystallisiert sie aus Alkohol um;
thiosaccharine
27148-03-4

thiosaccharine

KOH-solution

KOH-solution

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

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

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

saccharin
81-07-2

saccharin

KOH-solution

KOH-solution

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
beim Eindampfen;
N-(hydroxymethyl)saccharin
13947-20-1

N-(hydroxymethyl)saccharin

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 5 g / DAST / tetrahydrofuran / Ambient temperature
2: 59 percent / 5percent aq. NaOH / tetrahydrofuran
View Scheme
2-chloro-5-(chlorosulfonyl)benzoic acid
137-64-4

2-chloro-5-(chlorosulfonyl)benzoic acid

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

2-sulfamoylbenzoyl chloride

2-sulfamoylbenzoyl chloride

Conditions
ConditionsYield
With thionyl chloride at 0 - 80℃; for 2h;100%
methanol
67-56-1

methanol

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

methyl 2-(aminosulfonyl)benzoate
57683-71-3

methyl 2-(aminosulfonyl)benzoate

Conditions
ConditionsYield
With sulfuric acid
With hydrogenchloride
ethanol
64-17-5

ethanol

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

ethyl 2-(aminosulfonyl)benzoate
59777-72-9

ethyl 2-(aminosulfonyl)benzoate

Conditions
ConditionsYield
With sulfuric acid
With hydrogenchloride
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

ammonium thiocyanate
1147550-11-5

ammonium thiocyanate

2-carboxamidebenzenesulfonic acid
41363-39-7

2-carboxamidebenzenesulfonic acid

Conditions
ConditionsYield
at 90 - 100℃; 3 Tage lang, den zweiten auf 130-135grad, den dritten auf 150-160grad;
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

saccharin
81-07-2

saccharin

Conditions
ConditionsYield
at 114 - 116℃;
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

ethyl iodide
75-03-6

ethyl iodide

ethyl 2-(aminosulfonyl)benzoate
59777-72-9

ethyl 2-(aminosulfonyl)benzoate

Conditions
ConditionsYield
With sodium ethanolate
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

C7H6N2O6S

C7H6N2O6S

Conditions
ConditionsYield
With nitronium tetrafluoborate In acetonitrile at 20 - 25℃;
sulfuric acid
7664-93-9

sulfuric acid

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

sulfur trioxide
7446-11-9

sulfur trioxide

saccharin
81-07-2

saccharin

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

saccharin
81-07-2

saccharin

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

aqueous alkaline solution

aqueous alkaline solution

saccharin
81-07-2

saccharin

Conditions
ConditionsYield
hydrogenchloride
7647-01-0

hydrogenchloride

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

acid ammonium salt of/the/ 2-sulfo-benzoic acid

acid ammonium salt of/the/ 2-sulfo-benzoic acid

Conditions
ConditionsYield
at 20℃;
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

water
7732-18-5

water

acid ammonium salt of/the/ 2-sulfo-benzoic acid

acid ammonium salt of/the/ 2-sulfo-benzoic acid

Conditions
ConditionsYield
perchloric acid
7601-90-3

perchloric acid

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

A

saccharin
81-07-2

saccharin

B

acid ammonium salt of/the/ 2-sulfo-benzoic acid

acid ammonium salt of/the/ 2-sulfo-benzoic acid

Conditions
ConditionsYield
at 100℃;
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

A

saccharin
81-07-2

saccharin

B

acidic ammonium salt of/the/ o-sulfo-benzoic acid

acidic ammonium salt of/the/ o-sulfo-benzoic acid

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

ammonium thiocyanate
1147550-11-5

ammonium thiocyanate

ammonium salt of/the/ benzamide-o-sulfonic acid

ammonium salt of/the/ benzamide-o-sulfonic acid

Conditions
ConditionsYield
hydrogenchloride
7647-01-0

hydrogenchloride

ethanol
64-17-5

ethanol

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

o-sulfamide-benzoic acid ethyl ester

o-sulfamide-benzoic acid ethyl ester

Conditions
ConditionsYield
bildet sich zunaechst Saccharin;
ethanol
64-17-5

ethanol

sulfuric acid
7664-93-9

sulfuric acid

2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

o-sulfamide-benzoic acid ethyl ester

o-sulfamide-benzoic acid ethyl ester

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

sodium ethanolate
141-52-6

sodium ethanolate

ethyl iodide
75-03-6

ethyl iodide

o-sulfamide-benzoic acid ethyl ester

o-sulfamide-benzoic acid ethyl ester

Conditions
ConditionsYield
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

salts of saccharin

salts of saccharin

Conditions
ConditionsYield
die Salze reagieren;
2-sulfamoyl-benzoic acid
632-24-6

2-sulfamoyl-benzoic acid

3-(1-benzo[1,3]dioxol-5-yl-2-imidazol-1-yl-2-oxo-ethyl)-1-methyl-1H-indole-6-carboxylic acid methyl ester

3-(1-benzo[1,3]dioxol-5-yl-2-imidazol-1-yl-2-oxo-ethyl)-1-methyl-1H-indole-6-carboxylic acid methyl ester

3-[1-benzo[1,3]dioxol-5-yl-2-(2-carboxy-benzenesulfonylamino)-2-oxo-ethyl]-1-methyl-1H-indole-6-carboxylic acid methyl ester

3-[1-benzo[1,3]dioxol-5-yl-2-(2-carboxy-benzenesulfonylamino)-2-oxo-ethyl]-1-methyl-1H-indole-6-carboxylic acid methyl ester

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In dichloromethane for 12h; Heating;

632-24-6Relevant articles and documents

Antibacterial metal complexes of o-sulfamoylbenzoic acid: Synthesis, characterization, and DFT study

Ali, Akbar,Ashraf, Adnan,Hanif, Muhammad,Imran, Muhammad,Irfan, Ahmad,Khalid, Muhammad,Khan, Muhammad Usman,Parvez, Masood,Shafiq, Iqra,Sher, Falak,Siddiqui, Waseeq Ahmad

, (2021/10/07)

Herein, antibacterial transition metal complexes of ML2 type having o-sulfamoylbenzoic acid as ligand were synthesized from saccharin. All characterization techniques confirmed the syntheses of non-ionic transition metal MnII (3), CoII (4), NiII (5), CuII (6), and ZnII (7) complexes, where mono-anionic o-sulfamoylbenzoic acid acts as a weak field ligand. The FT-IR, elemental analysis, and magnetic susceptibility studies suggested octahedral and square pyramidal geometries depending on the nature of metal ions. Biological activity of these complexes was studied by using six bacterial strains. Interestingly, the bacterial strains Escherichia coli and Klebsiella aerogenes were inhibited to the maximum level by 6. Among aforementioned five complexes, 4 and 6 were found in crystalline form. Apart from experimental study, DFT study was also performed for entitled complexes at the M06/6-311G(d,p) level. A comparative investigation was performed for geometrical parameters and vibrational analysis, and an agreement was obtained. Natural bonding orbital investigations expressed larger value of stabilization energy 21 kcal/mol for 3, 4, and 6 while 42 kcal/mol for 5 and 7. Furthermore, global reactivity findings also disclosed higher value of hardness (2.44–3.09 eV) for entitled chromophores, hence, showed more stability. Moreover, frontier molecular orbital (FMO) findings revealed a larger band gap (4.48–6.19 eV) with higher values of LUMO found for all complexes.

Sulfamylbenzoic acids

-

, (2008/06/13)

Certain mono- and disubstituted-5-sulfamylbenzoic acids, many of which are novel, and their use in lowering blood lipid levels in mammals.

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