3-Amino-N,N-diethyl-4-methoxybenzenesulfonamide structure
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Common Name | 3-Amino-N,N-diethyl-4-methoxybenzenesulfonamide | ||
|---|---|---|---|---|
| CAS Number | 97-35-8 | Molecular Weight | 258.337 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 410.6±55.0 °C at 760 mmHg | |
| Molecular Formula | C11H18N2O3S | Melting Point | 102-105°C | |
| MSDS | USA | Flash Point | 202.1±31.5 °C | |
Use of 3-Amino-N,N-diethyl-4-methoxybenzenesulfonamideFast Red ITR is a nonlinear optical material[1]. Fast Red ITR can be used in alkaline phosphatase histochemistry[1][2]. |
| Name | Fast Red Itr Base |
|---|---|
| Synonym | More Synonyms |
| Description | Fast Red ITR is a nonlinear optical material[1]. Fast Red ITR can be used in alkaline phosphatase histochemistry[1][2]. |
|---|---|
| Related Catalog | |
| References |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 410.6±55.0 °C at 760 mmHg |
| Melting Point | 102-105°C |
| Molecular Formula | C11H18N2O3S |
| Molecular Weight | 258.337 |
| Flash Point | 202.1±31.5 °C |
| Exact Mass | 258.103821 |
| PSA | 81.01000 |
| LogP | 1.65 |
| Vapour Pressure | 0.0±1.0 mmHg at 25°C |
| Index of Refraction | 1.547 |
| InChIKey | WBGVVXSCGNGJFL-UHFFFAOYSA-N |
| SMILES | CCN(CC)S(=O)(=O)c1ccc(OC)c(N)c1 |
| Hazard Codes | F,T,N |
|---|---|
| Risk Phrases | R45:May cause cancer. R11:Highly Flammable. R23/24/25:Toxic by inhalation, in contact with skin and if swallowed . R37/38:Irritating to respiratory system and skin . R41:Risk of serious damage to eyes. R43:May cause sensitization by skin contact. R51/53:To |
| Safety Phrases | S53-S9-S16-S45-S61-S36/37 |
| RIDADR | UN 1093 3/PG 1 |
| WGK Germany | 3 |
| RTECS | AT5250000 |
| Packaging Group | I |
| Hazard Class | 3 |
| HS Code | 29261000 |
| Precursor 0 | |
|---|---|
| DownStream 1 | |
| HS Code | 2935009090 |
|---|---|
| Summary | 2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0% |
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Class I histone deacetylases 1, 2 and 3 are highly expressed in renal cell cancer.
BMC Cancer 8 , 381, (2008) Enhanced activity of histone deacetylases (HDAC) is associated with more aggressive tumour behaviour and tumour progression in various solid tumours. The over-expression of these proteins and their kn... |
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Tobacco rattle virus 16-kilodalton protein encodes a suppressor of RNA silencing that allows transient viral entry in meristems.
J. Virol. 82(8) , 4064-71, (2008) RNA silencing is a host defense mechanism that limits the accumulation and spread of viruses in infected plants. Correspondingly, plant viruses encode suppressors of silencing. In the positive-strand ... |
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Regulation of expression and function of dipeptidyl peptidase 4 (DP4), DP8/9, and DP10 in allergic responses of the lung in rats.
J. Histochem. Cytochem. 56 , 147-55, (2008) The expression of dipeptidyl peptidase 4 (DP4, CD26) affects T-cell recruitment to lungs in an experimental rat asthma model. Furthermore, the gene of the structural homologous DP10 represents a susce... |
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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
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Name: Luminescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id: OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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Name: QFRET-based biochemical primary high throughput screening assay to identify exosite i...
Source: The Scripps Research Institute Molecular Screening Center
Target: disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id: ADAM17_INH_QFRET_1536_1X%INH PRUN
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Name: Fluorescence-based cell-based primary high throughput screening assay to identify ago...
Source: The Scripps Research Institute Molecular Screening Center
Target: muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id: CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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Name: Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
Source: Broad Institute
Target: FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id: 2147-01_Inhibitor_SinglePoint_HTS_Activity
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Name: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
Source: Broad Institute
Target: N/A
External Id: Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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Name: Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
Source: Broad Institute
Target: N/A
External Id: 7124-01_Inhibitor_SinglePoint_HTS_Activity
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Name: qHTS of TDP-43 Inhibitors: NCGC Sytravon Library Screen
Source: NCGC
External Id: tdp43-p2-repeat
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| EINECS 202-575-5 |
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