478563
2-氨基-6-氯-9H-嘌呤-9-乙酸
97%
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关于此项目
经验公式（希尔记法）:
C7H6ClN5O2
化学文摘社编号:
分子量:
227.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C7H6ClN5O2/c8-5-4-6(12-7(9)11-5)13(2-10-4)1-3(14)15/h2H,1H2,(H,14,15)(H2,9,11,12)
SMILES string
Nc1nc(Cl)c2ncn(CC(O)=O)c2n1
InChI key
LRZBBTTUKFVUMZ-UHFFFAOYSA-N
assay
97%
mp
>300 °C (lit.)
functional group
carboxylic acid, chloro
General description
2-Amino-6-chloro-9H-purine-9-acetic acid is a purine derivative.
Application
2-Amino-6-chloro-9H-purine-9-acetic acid may be used as starting material in the synthesis of:
- 6-decyloxy substituted purine intermediates
- 6-decylthio substituted purine intermediates
- 6-decyloxy or 6-decylthio-9-phenylalanine/serine or alanine-substituted purine derivatives
- 2,6-diaminopurine monomer
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Damian Ackermann et al.
Nucleic acids research, 41(8), 4729-4739 (2013-02-28)
The structural reorganization of nanoscale DNA architectures is a fundamental aspect in dynamic DNA nanotechnology. Commonly, DNA nanoarchitectures are reorganized by means of toehold-expanded DNA sequences in a strand exchange process. Here we describe an unprecedented, toehold-free switching process that
Ashish K Pathak et al.
Bioorganic & medicinal chemistry, 21(7), 1685-1695 (2013-02-26)
6-Oxo and 6-thio analogs of purine were prepared based on the initial activity screening of a small, diverse purine library against Mycobacterium tuberculosis (Mtb). Certain 6-oxo and 6-thio-substituted purine analogs described herein showed moderate to good inhibitory activity. N(9)-substitution apparently
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