CAS
5742-07-4 Purity
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5742-07-4 Purity
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![(Z)-7-[(1R,2S,3R,5S)-5-Acetoxy-2-hydroxymethyl-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-hept-5-enoic acid methyl ester](https://resource.alfa-chemistry.com/structure/57429-54-6.gif)
![(Z)-7-[(1R,2R,3R,5S)-5-Acetoxy-2-formyl-3-(tetrahydro-pyran-2-yloxy)-cyclopentyl]-hept-5-enoic acid methyl ester](https://resource.alfa-chemistry.com/structure/57429-55-7.gif)
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6-Thioinosine
CAS
574-25-4
Catalog Number
ACM574254
Category
Other Products
Molecular Weight
284.29
Molecular Formula
C10H12N4O4S
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Specification
Synonyms
Thionosine, Tioinosine, 6-Thioinosine, THIOINOSINE, 6-Mercaptoinosine, 6-MP-Riboside, Inosine, 6-thio-, Ribosyl-6-thiopurine, 6-Thiopurine riboside, Mercaptopurine riboside, 6-mercaptopurine riboside, Thioinosine (JAN), Thioinosine [JAN], 6-Purinethiol riboside, 6-Thiopurine ribonucleoside, Ribosyl-6-mercaptopurine, Mercaptopurine ribonucleoside, 6-MPR, 6-Mercaptopurine ribonucleoside, CCRIS 2763
IUPAC Name
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purine-6-thione
Canonical SMILES
C1=NC(=S)C2=C(N1)N(C=N2)C3C(C(C(O3)CO)O)O
InChI Key
NKGPJODWTZCHGF-KQYNXXCUSA-N
Boiling Point
714.7ºC at 760mmHg
Melting Point
220-223ºC(lit.)
Flash Point
386ºC
Density
2.02g/cm³
EC Number
209-371-5
Exact Mass
284.05800
Hazard Statements
Xn
H-Bond Acceptor
6
H-Bond Donor
4
Stability
Store in Cool Dry Place
Upstream Synthesis Route 1
- 67-56-1
- 38048-32-7
- 107-03-9
- 100-27-6
- 91012-47-4
- 574-25-4
- 92035-03-5
- 143330-49-8
- 143330-48-7
Reference: [1] Journal of Organic Chemistry, 1992, vol. 57, # 22, p. 5968 - 5976
Upstream Synthesis Route 2
- 67-56-1
- 38048-32-7
- 107-03-9
- 100-27-6
- 91012-47-4
- 574-25-4
- 92035-03-5
- 143330-49-8
- 143330-48-7
Reference: [1]Journal of Organic Chemistry,1992,vol. 57,p. 5968 - 5976
Downstream Synthesis Route 1
- 100-39-0
- 574-25-4
- 6165-03-3
Reference: [1]Journal of Organic Chemistry,1992,vol. 57,p. 5968 - 5976
Downstream Synthesis Route 2
- 106-94-5
- 574-25-4
- 92035-03-5
Reference: [1]Journal of Organic Chemistry,1992,vol. 57,p. 5968 - 5976
* For details of the synthesis route, please refer to the original source to ensure accuracy.
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