ChemicalBook > Product Catalog > Organic Chemistry > Carboxylic acids and derivatives > N1-Acetylsulfamethoxazol
N1-Acetylsulfamethoxazol
N1-Acetylsulfamethoxazol Basic information
- Product Name:
- N1-Acetylsulfamethoxazol
- Synonyms:
-
- N1-Acetylsulfamethoxazol
- (S)-2-(6-aminobenzo[d]thiazol-2-yl)-4,5-dihydrothiazole-4-carboxylic acid
- 4-Thiazolecarboxylic acid, 2-(6-amino-2-benzothiazolyl)-4,5-dihydro-, (4S)-
- 6'-Amino-D-luciferin >=95.0% (HPLC)
- Aminoluciferin
- aLuc
- Aminoluciferin[firefly]
- 6′-Amino-
D -luciferin
- CAS:
- 161055-47-6
- MF:
- C11H9N3O2S2
- MW:
- 279.34
- Mol File:
- 161055-47-6.mol
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N1-Acetylsulfamethoxazol Chemical Properties
- Boiling point:
- 594.9±60.0 °C(Predicted)
- Density
- 1.81±0.1 g/cm3(Predicted)
- storage temp.
- -20°C
- pka
- 3.47±0.20(Predicted)
- form
- Solid
- color
- Light yellow to brown
- InChI
- InChI=1S/C11H9N3O2S2/c12-5-1-2-6-8(3-5)18-10(13-6)9-14-7(4-17-9)11(15)16/h1-3,7H,4,12H2,(H,15,16)/t7-/m1/s1
- InChIKey
- HKSJKXOOBAVPKR-SSDOTTSWSA-N
- SMILES
- S1C[C@H](C(O)=O)N=C1C1=NC2=CC=C(N)C=C2S1
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N1-Acetylsulfamethoxazol Usage And Synthesis
Uses
6’-Amino-D-luciferin is a D-luciferin (HY-12591A) with its 6-position hydroxyl group substituted with an amino group. D-luciferin is the natural substrate of the enzyme luciferase (Luc)[1].
References
[1] Kovács AK, et al. Synthesis of N-peptide-6-amino-D-luciferin Conjugates. Front Chem. 2018 Apr 19;6:120. DOI:10.3389/fchem.2018.00120
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