Catalog No.:AA001TT2

16321-99-6 | 2-Amino-6-chloro-9-(2,3,5-tri-o-acetyl-beta-d-ribofuranosyl)purine

Name: Name:2-Amino-6-chloro-9-(2,3,5-tri-o-acetyl-beta-d-ribofuranosyl)purine
Brand: AABLOCKS
SKU: AA001TT2
Availability: InStock
Rating: 90 (10 reviews)

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Quantity

250mg

98+%

in stock

$23.00 $16.00

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98+%

in stock

$50.00 $35.00

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98+%

in stock

$164.00 $115.00

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25g

98+%

in stock

$573.00 $401.00

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Technical Information
Properties
Literature
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Technical Information
Properties
Literature

Technical Information

Catalog Number:

AA001TT2

Chemical Name:

2-Amino-6-chloro-9-(2,3,5-tri-o-acetyl-beta-d-ribofuranosyl)purine

CAS Number:

16321-99-6

Molecular Formula:

C16H18ClN5O7

Molecular Weight:

427.7964

MDL Number:

MFCD03425473

SMILES:

CC(=O)O[C@@H]1[C@H](OC(=O)C)[C@H](O[C@H]1n1cnc2c1nc(N)nc2Cl)COC(=O)C

Properties

BP:

637°C at 760 mmHg

Form:

Solid

MP:

140-142°C

Storage:

Keep in dry area;2-8℃;

Computed Properties

Complexity:

655

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.2

Literature

Title: Nucleic acid related compounds. 118. Nonaqueous diazotization of aminopurine derivatives. Convenient access to 6-halo- and 2,6-dihalopurine nucleosides and 2'-deoxynucleosides with acyl or silyl halides.

Journal: The Journal of organic chemistry 20030124

Title: Nucleic acid related compounds. 116. Nonaqueous diazotization of aminopurine nucleosides. Mechanistic considerations and efficient procedures with tert-butyl nitrite or sodium nitrite.

Journal: The Journal of organic chemistry 20020920

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