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About This Item
Empirical Formula (Hill Notation):
C10H12N4O4S
CAS Number:
Molecular Weight:
284.29
EC Number:
209-371-5
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
40536
MDL number:
grade
purum
optical activity
[α]20/D −74±3°, c = 1% in 0.1 M NaOH
impurities
≤5% water
mp
220-223 °C
SMILES string
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(S)ncnc23
InChI
1S/C10H12N4O4S/c15-1-4-6(16)7(17)10(18-4)14-3-13-5-8(14)11-2-12-9(5)19/h2-4,6-7,10,15-17H,1H2,(H,11,12,19)/t4-,6-,7-,10-/m1/s1
InChI key
NKGPJODWTZCHGF-KQYNXXCUSA-N
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
Nucleoside analogue; building block used for the synthesis of N6-alkylated adenosines by reaction with an amine
Regulatory Information
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Affinity chromatography on immobilised adenosine 5'-monophosphate. 1. A new synthesis and some properties of an N6-immobilised 5'-AMP.
D B Craven et al.
European journal of biochemistry, 41(2), 329-333 (1974-01-16)
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