ChemicalBook--->CAS DataBase List--->161055-47-6

161055-47-6

161055-47-6 Structure

161055-47-6 Structure
IdentificationBack Directory
[Name]

N1-Acetylsulfamethoxazol
[CAS]

161055-47-6
[Synonyms]

aLuc
Aminoluciferin
Aminoluciferin[firefly]
N1-Acetylsulfamethoxazol
6'-Amino-D-luciferin >=95.0% (HPLC)
(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)-
[Molecular Formula]

C11H9N3O2S2
[MDL Number]

MFCD29912852
[MOL File]

161055-47-6.mol
[Molecular Weight]

279.34
Chemical PropertiesBack Directory
[Boiling point ]

594.9±60.0 °C(Predicted)
[density ]

1.81±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[form ]

Solid
[pka]

3.47±0.20(Predicted)
[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
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[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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