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About This Item
经验公式（希尔记法）:
C3H4N2 · CHF3O3S
CAS号:
分子量:
218.15
MDL號碼:
分類程式碼代碼:
12352005
eCl@ss:
39161001
PubChem物質ID:
NACRES:
NA.22
推荐产品
化驗
97%
mp
189-193 °C (lit.)
SMILES 字串
c1c[nH]cn1.OS(=O)(=O)C(F)(F)F
InChI
1S/C3H4N2.CHF3O3S/c1-2-5-3-4-1;2-1(3,4)8(5,6)7/h1-3H,(H,4,5);(H,5,6,7)
InChI 密鑰
JNJFONBBNLVENC-UHFFFAOYSA-N
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Stéphane Bernier et al.
Bioorganic & medicinal chemistry, 13(1), 69-75 (2004-12-08)
Three nonhydrolyzable aspartyl adenylate analogs have been prepared and tested as inhibitors of E. coli aspartyl-tRNA synthetase. 5'-O-[N-(L-Aspartyl)sulfamoyl]adenosine is a potent competitive inhibitor (K(i) = 15 nM) whereas L-aspartol adenylate is a weaker inhibitor (K(i) = 45 microM) with respect
S Iwai et al.
Nucleic acids research, 27(11), 2299-2303 (1999-05-15)
In the solid-phase synthesis of oligonucleotides containing the pyrimidine(6-4)pyrimidone photoproduct using a dinucleotide building block, considerable amounts of by-products were found as the chain length increased. The by-products were the major product when a 49mer was synthesized on a 40
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