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41602-56-6

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41602-56-6 Usage

General Description

4-(Dimethylamino)salicylaldehyde, also known as DASAL, is a chemical compound derived from salicylaldehyde and dimethylamine. It is a yellow solid that is commonly used in the pharmaceutical and research industries as a fluorescent dye for detecting and quantifying biological molecules, such as proteins and amino acids. DASAL is also utilized in the development of sensors and probes for detecting metals and other analytes in environmental and biological samples. Its unique fluorescent properties make it a valuable tool in various biochemical and analytical applications. Additionally, DASAL has been investigated for its potential therapeutic and medicinal properties, with studies suggesting its potential anti-cancer and anti-inflammatory effects. Overall, 4-(dimethylamino)salicylaldehyde is a versatile compound with diverse applications in research, medicine, and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 41602-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,0 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41602-56:
(7*4)+(6*1)+(5*6)+(4*0)+(3*2)+(2*5)+(1*6)=86
86 % 10 = 6
So 41602-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-10(2)8-4-3-7(6-11)9(12)5-8/h3-6,12H,1-2H3

41602-56-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Dimethylamino)-2-hydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(dimethylamino)-2-hydroxybenzaldehyde

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:41602-56-6 SDS

41602-56-6Synthetic route

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

N,N-dimethyl-formamide

3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-formamide With trichlorophosphate for 0.0833333h;
Stage #2: 3-Dimethylaminophenol at 20 - 70℃; for 2h;
100%
With methanesulfonyl chloride at 20 - 100℃; for 1h;90.9%
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 20℃; Inert atmosphere;
Stage #2: 3-Dimethylaminophenol at 20 - 90℃; Vilsmeier-Haack reaction; Inert atmosphere;
Stage #3: With water
70%
5-dimethylamino-2-(1,3-diphenyl-imidazolidin-2-yl)-phenol
58343-05-8

5-dimethylamino-2-(1,3-diphenyl-imidazolidin-2-yl)-phenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
With hydrogenchloride; water at 25℃; for 2h;90%
orthoformic acid triethyl ester
122-51-0

orthoformic acid triethyl ester

3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
With aluminium trichloride In chloroform for 0.166667h; Ambient temperature;65%
formaldehyd
50-00-0

formaldehyd

3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

3-<<(diethylamino)carbonyl>oxy>-N,N-dimethylaniline
63907-38-0

3-<<(diethylamino)carbonyl>oxy>-N,N-dimethylaniline

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

N,N-dimethyl-formamide

A

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

B

5-(dimethylamino)-2-formylphenyl diethylcarbamate
96649-22-8

5-(dimethylamino)-2-formylphenyl diethylcarbamate

Conditions
ConditionsYield
With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium 1.) cyclohexane, THF, -78 deg C, 1 h, 2.) a) -78 deg C, 4 h, b) from -78 deg C to RT, 2 h, c) RT, 0.5 h; Yield given. Multistep reaction. Yields of byproduct given;
2-Benzoyloxy-4-(N,N-dimethylamino)-benzaldehyd
24589-97-7

2-Benzoyloxy-4-(N,N-dimethylamino)-benzaldehyd

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
(alkaline hydrolysis);
3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

<3.6-bis-diethylamino-9-oxy-xanthyl>-benzene-pentacarboxylic acid

<3.6-bis-diethylamino-9-oxy-xanthyl>-benzene-pentacarboxylic acid

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) sodium hydride / 1.) diethyl ether, DMF, 15 min, 2.) RT, 1.5 h
2: 1.) sec-BuLi, TMEDA / 1.) cyclohexane, THF, -78 deg C, 1 h, 2.) a) -78 deg C, 4 h, b) from -78 deg C to RT, 2 h, c) RT, 0.5 h
View Scheme
3-(dimethylamino)phenyl benzoate
157279-47-5

3-(dimethylamino)phenyl benzoate

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (formylation)
2: (alkaline hydrolysis)
View Scheme
Vilsmeier reagent
3724-43-4, 149409-22-3

Vilsmeier reagent

3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 60 - 70℃; for 1h;
3-Dimethylaminophenol
99-07-0

3-Dimethylaminophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: chlorobenzene / 6 h / 100 °C / Inert atmosphere
2: hydrogenchloride; water / 2 h / 25 °C
View Scheme
ethyl bromide
74-96-4

ethyl bromide

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

4-(dimethylamino)-2-ethoxybenzaldehyde

4-(dimethylamino)-2-ethoxybenzaldehyde

Conditions
ConditionsYield
With 18-crown-6 ether; potassium carbonate In acetone at 40℃; for 16h;100%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

acetyl chloride
75-36-5

acetyl chloride

5-(dimethylamino)-2-formylphenyl acetate
174269-30-8

5-(dimethylamino)-2-formylphenyl acetate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;99%
C36H42Br2N6O4
1266669-75-3

C36H42Br2N6O4

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

zinc(II) acetate dihydrate
5970-45-6

zinc(II) acetate dihydrate

C54H58Br2N8O6Zn

C54H58Br2N8O6Zn

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 4h; Inert atmosphere;95%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

cyanoacetic acid amide
107-91-5

cyanoacetic acid amide

7-Dimethylamino-2-imino-2H-chromene-3-carboxylic acid amide
79604-92-5

7-Dimethylamino-2-imino-2H-chromene-3-carboxylic acid amide

Conditions
ConditionsYield
With piperidine In ethanol Heating;93%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

tert.-butyl lithium
594-19-4

tert.-butyl lithium

5-(dimethylamino)-2-(1-hydroxy-2,2-dimethylpropyl)phenol
1322596-77-9

5-(dimethylamino)-2-(1-hydroxy-2,2-dimethylpropyl)phenol

Conditions
ConditionsYield
In tetrahydrofuran; pentane at -78 - 20℃; Inert atmosphere;92%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

(E)-4-(dimethylamino)-2-hydroxybenzaldehyde oxime

(E)-4-(dimethylamino)-2-hydroxybenzaldehyde oxime

Conditions
ConditionsYield
With pyridine; hydroxylamine hydrochloride In ethanol at 60℃; for 3h; Inert atmosphere;92%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

acetoacetic acid methyl ester
105-45-3

acetoacetic acid methyl ester

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one
74696-95-0

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one

Conditions
ConditionsYield
With piperidine In ethanol for 3h; Reflux;92%
4-Fluorothiophenol
371-42-6

4-Fluorothiophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

malononitrile
109-77-3

malononitrile

2,4-diamino-8-(dimethylamino)-5-((4-fluorophenyl)thio)-5H-chromeno[2,3-b]pyridine-3-carbonitrile

2,4-diamino-8-(dimethylamino)-5-((4-fluorophenyl)thio)-5H-chromeno[2,3-b]pyridine-3-carbonitrile

Conditions
ConditionsYield
With triethylamine In ethanol for 4h; Temperature; Reflux;90%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

3,4-dihydro-2H-benzo[b][1,4]dioxepine-7-carbohydrazide

3,4-dihydro-2H-benzo[b][1,4]dioxepine-7-carbohydrazide

(E)-N'-(4-(dimethylamino)-2-hydroxybenzylidene)-3,4-dihydro-2H-benzo[b][1,4]dioxepine-7-carbohydrazide

(E)-N'-(4-(dimethylamino)-2-hydroxybenzylidene)-3,4-dihydro-2H-benzo[b][1,4]dioxepine-7-carbohydrazide

Conditions
ConditionsYield
With acetic acid In ethanol for 5h; Reflux;90%
Cyclopentyl bromide
137-43-9

Cyclopentyl bromide

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

2-(cyclopentoxy)-4-(dimethylamino)benzaldehyde

2-(cyclopentoxy)-4-(dimethylamino)benzaldehyde

Conditions
ConditionsYield
With 18-crown-6 ether; potassium carbonate In acetone for 24h; Inert atmosphere; Reflux;89.2%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

dimedone
126-81-8

dimedone

malononitrile
109-77-3

malononitrile

2-amino-4-(4-(dimethylamino)-2-hydroxyphenyl)-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile

2-amino-4-(4-(dimethylamino)-2-hydroxyphenyl)-7,7-dimethyl-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile

Conditions
ConditionsYield
With potassium tert-butylate In tetrahydrofuran; methanol at 20℃;89%
N,N-dimethyl-4-aminothiophenol
4946-22-9

N,N-dimethyl-4-aminothiophenol

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

malononitrile
109-77-3

malononitrile

2,4-diamino-8-(dimethylamino)-5-((4-(dimethylamino)phenyl)thio)-5H-chromeno[2,3-b]pyridine-3-carbonitrile

2,4-diamino-8-(dimethylamino)-5-((4-(dimethylamino)phenyl)thio)-5H-chromeno[2,3-b]pyridine-3-carbonitrile

Conditions
ConditionsYield
With triethylamine In ethanol for 4h; Temperature; Reflux;88%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

benzyl bromide
100-39-0

benzyl bromide

C16H17NO2
1268353-44-1

C16H17NO2

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 8h;87.6%
2,6-diisopropylbenzenamine
24544-04-5

2,6-diisopropylbenzenamine

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

C21H28N2O

C21H28N2O

Conditions
ConditionsYield
With acetic acid In ethanol for 2h; Reflux;87%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

ethyl (triphenylphosphoranylidene)acetate
1099-45-2

ethyl (triphenylphosphoranylidene)acetate

7-(N,N-dimethylamino)-2-oxo-2H-chromene

7-(N,N-dimethylamino)-2-oxo-2H-chromene

Conditions
ConditionsYield
at 170 - 180℃; for 1h;86%
at 180℃; for 1h; Inert atmosphere;77%
at 180℃; for 1h; Inert atmosphere;62%
at 180℃; for 1h; Inert atmosphere;62%
N,N′-bisoctadecyl-L-aminoglutamicdiamide
752950-25-7

N,N′-bisoctadecyl-L-aminoglutamicdiamide

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

C50H92N4O3

C50H92N4O3

Conditions
ConditionsYield
In ethanol at 80℃; for 8h;85%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one
74696-95-0

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one

7,7'-Bis-dimethylamino-2'-oxo-2'H-[2,3']bichromenyl-1-ylium; perchlorate

7,7'-Bis-dimethylamino-2'-oxo-2'H-[2,3']bichromenyl-1-ylium; perchlorate

Conditions
ConditionsYield
With perchloric acid In acetic acid for 0.5h; Heating;83%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one
74696-95-0

3-acetyl-7-(dimethylamino)-2H-1-benzopyran-2-one

Conditions
ConditionsYield
With piperidine In ethanol for 6h; Heating / reflux;81%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

malononitrile
109-77-3

malononitrile

3-cyano-7-dimethylaminocoumarin
53050-52-5

3-cyano-7-dimethylaminocoumarin

Conditions
ConditionsYield
Stage #1: 4-dimethylamino-2-hydroxy-benzaldehyde; malononitrile With sodium hydroxide In water at 20℃; for 1.5h;
Stage #2: With hydrogenchloride In water for 1h; Reflux;
81%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

m-phenylenediamine
108-45-2

m-phenylenediamine

6,6'-((1,3-phenylenebis(azanylylidene))bis(methanylylidene))bis(3-(dimethylamino)phenol)

6,6'-((1,3-phenylenebis(azanylylidene))bis(methanylylidene))bis(3-(dimethylamino)phenol)

Conditions
ConditionsYield
In ethanol for 5h; Reflux;79%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

7,7'-Bis-dimethylamino-2'-oxo-2'H-[2,3']bichromenyl-1-ylium; perchlorate

7,7'-Bis-dimethylamino-2'-oxo-2'H-[2,3']bichromenyl-1-ylium; perchlorate

Conditions
ConditionsYield
With perchloric acid In acetic acid for 0.5h; Heating;76%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

1-ethynylcyclobutan-1-ol
98135-75-2

1-ethynylcyclobutan-1-ol

2-(2-(4-(dimethylamino)-2-hydroxyphenyl)-2-oxoethyl)cyclopentanone

2-(2-(4-(dimethylamino)-2-hydroxyphenyl)-2-oxoethyl)cyclopentanone

Conditions
ConditionsYield
With [Rh(OH)(cod)]2; triphenylphosphine In 1,2-dichloro-ethane at 70℃; for 12h; Sealed tube;76%
indole-2-carbohydrazide
5055-39-0

indole-2-carbohydrazide

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

N'-{[4-(dimethylamino)-2-hydroxyphenyl]methylidene}-1H-indole-2-carbohydrazide

N'-{[4-(dimethylamino)-2-hydroxyphenyl]methylidene}-1H-indole-2-carbohydrazide

Conditions
ConditionsYield
In ethanol Reflux;76%
phenylacetic acid
103-82-2

phenylacetic acid

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

3-phenyl-7-(N,N-dimethylamino)coumarin

3-phenyl-7-(N,N-dimethylamino)coumarin

Conditions
ConditionsYield
With 2-chloro-1-methyl-pyridinium iodide; triethylamine In acetonitrile for 2h; Heating;75%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

C20H31NO5

C20H31NO5

C29H39N2O5(1+)*ClO4(1-)

C29H39N2O5(1+)*ClO4(1-)

Conditions
ConditionsYield
With sulfuric acid at 100℃; for 2h;74%
1H-indole-3-carboxylic acid hydrazide
15317-58-5

1H-indole-3-carboxylic acid hydrazide

4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

N'-{[4-(dimethylamino)-2-hydroxyphenyl]methylidene}-1H-indole-3-carbohydrazide

N'-{[4-(dimethylamino)-2-hydroxyphenyl]methylidene}-1H-indole-3-carbohydrazide

Conditions
ConditionsYield
In ethanol Reflux;73%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

(carbethoxyethylidene)triphenylphosphorane
21382-82-1

(carbethoxyethylidene)triphenylphosphorane

7-(dimethylamino)-3-methylcoumarin

7-(dimethylamino)-3-methylcoumarin

Conditions
ConditionsYield
at 180℃; for 2h;72%
4-dimethylamino-2-hydroxy-benzaldehyde
41602-56-6

4-dimethylamino-2-hydroxy-benzaldehyde

acetic anhydride
108-24-7

acetic anhydride

5-(dimethylamino)-2-formylphenyl acetate
174269-30-8

5-(dimethylamino)-2-formylphenyl acetate

Conditions
ConditionsYield
With pyridine In dichloromethane at 20℃; for 1h;71%

41602-56-6Relevant articles and documents

Turn on ESPT: Novel salicylaldehyde based sensor for biological important fluoride sensing

Liu, Kai,Zhao, Xiaojun,Liu, Qingxiang,Huo, Jianzhong,Fu, Huifang,Wang, Ying

, p. 75 - 79 (2014)

A novel and simple salicylaldehyde based anion fluorescent sensor 1 has been designed, which can selectively sense fluoride by 'turn on' excited-state intermolecular proton transfer (ESPT). The binding constant and the stoichiometry were obtained by non-linear least-square analysis of the titration curves.

Anagostic interactions in chiral separation. Polymorphism in a [Co(II)(L)] complex: Crystallographic and theoretical studies

Awwadi, Firas F.,Hodali, Hamdallah A.

, p. 373 - 381 (2018)

Syntheses and crystal structures of two polymorphs of the complex [Co(II)(L)], where H2L = 2,2’-[cis-1,2-diaminocyclohexanediylbis (nitrilo-methylidyne)]bis (5-dimethyl-amino]phenol, have been studied. The two polymorphs concomitantly crystallized by vapour diffusion of solvent. The first polymorph (I) crystallized as a racemate in the centrosymmetric tetragonal I41/a space group. The second polymorph (II) crystallized in the chiral orthorhombic space group P212121. The chiral conformers of symmetrical cis-1,2-disubstituted cyclohexane molecules cannot be resolved in the liquid or gas phases, due to the rapid ring inversion. In the present study, the two chiral conformers are present in crystals of polymorph I, whereas, only one chiral conformer is present in crystals of polymorph II. Crystal structure analysis indicated that the formation of two different polymorphs of [Co(II)(L)] complex can be rationalized based on C–H?Co anagostic interactions. Density Functional Theory (DFT) calculations indicated that C–H?Co interactions are due to HOMO-LUMO interactions.

Imidazolyl–benzocoumarins as ratiometric fluorescence probes for biologically extreme acidity

Kim, Hyerim,Sarkar, Sourav,Nandy, Madhurima,Ahn, Kyo Han

, (2021)

A rational approach to develop a fluorescent probe for sensing biologically “extreme” acidity (pH a = 1.3 among ratiometric probes known so far, which is ascribed due to a unique sensing mechanism. The probe has high quantum yields, high chemical stability and good aqueous solubility. The probe was successfully applied to ratiometric fluorescence imaging of intrabacterial acidity from pH 4.0–1.0, offering a practical means for studying biological systems under the extreme pH conditions.

Fluoride-driven 'turn on' ESPT in the binding with a novel benzimidazole-based sensor

Liu, Kai,Zhao, Xiaojun,Liu, Qingxiang,Huo, Jianzhong,Zhu, Bolin,Diao, Shihua

, p. 563 - 567 (2015)

A novel fluorescence sensor (BIP) bearing NH and OH subunits displayed a highly selective and sensitive recognition property for fluoride over other anions. Fluoride-driven ESPT, poorly used in anion recognition and sensing, was suggested to be responsible for the fluorescence enhancement with a blue shift of 35 nm in the emission spectrum.

ACYL SULFONAMIDES FOR TREATING CANCER

-

Page/Page column 305, (2020/11/03)

The present invention provides acyl sulfonamide compounds of general formula (I): in which X, R1, R2, R3, R4, R5, R6, Ra and Rb are as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, as a sole agent or in combination with other active ingredients as well as methods of treating and/or prophylaxing diseases, particularly cancer, more particularly cancer in which KAT6A and/or KAT6B is focally amplified, said method comprising administering an effective amount of at least one compound of formula (I) to a subject in need thereof.

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