30426-58-5 ((Acetyl chloride, azido-)

快速询单

结构式：

Acetyl chloride, azido-MOL文件

CAS号：

30426-58-5

英文名称：

Acetyl chloride, azido-

分子式：

C₂H₂ClN₃O

分子量：

119.509778499603

Acetyl chloride, azido-(30426-58-5)名称与标识符

名称

英文别名：

Acetyl chloride, azido-;2-azidoacetyl chloride;azidoacetyl chloride;30426-58-5;EN300-736796;DTXSID60447932;SUHXTVABLHHRST-UHFFFAOYSA-N;SCHEMBL18699270;N3CH2COCl;azidoacetylchloride;Acetyl chloride, 2-azido-;

标识符

InChIKey：

SUHXTVABLHHRST-UHFFFAOYSA-N

Inchi：

1S/C2H2ClN3O/c3-2(7)1-5-6-4/h1H2

SMILES：

ClC(CN=[N+]=[N-])=O

Acetyl chloride, azido-(30426-58-5)物化性质

实验特性

PSA : 65.83

计算特性

精确分子量 : 118.98876
氢键供体数量 : 0
氢键受体数量 : 3
可旋转化学键数量 : 2
同位素质量 : 118.9886394g/mol
重原子数量 : 7
复杂度 : 116
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
疏水参数计算参考值（XlogP） : 1.9
拓扑分子极性表面积 : 31.4Å²

Acetyl chloride, azido-(30426-58-5)相关文献

1. Studies on lactams. Part XIV. The synthesis of a structural isomer of penicillin
Ajay K. Bose,G. Spiegelman,M. S. Manhas J. Chem. Soc. C 1971 2468
2. Studies on lactams. Part XIII. A position isomer of a penam (4-thia-1-aza-bicyclo[3,2,0]heptane)
Ajay K. Bose,G. Spiegelman,M. S. Manhas J. Chem. Soc. C 1971 188
3. Studies related to penicillins and cephalosporins. Part 6. Synthesis of the (±)-dinorpenicillin-spirocyclopentane system
Mario D. Bachi,Sabar Sasson,Jacob Vaya J. Chem. Soc. Perkin Trans. 1 1980 2228
4. New polycyclic β-lactams. Synthesis of 2a,3-dihydroazeto[1,2-a]quinoline-1,4(2H)-diones, structural analogues of the carbacephalosporin antibiotics
Mario D. Bachi,Joseph Klein J. Chem. Soc. Perkin Trans. 1 1983 1925
5. Studies related to penicillins and cephalosporins. Part 5. A new relay synthesis of penicillin
Mario D. Bachi,Ron Breiman J. Chem. Soc. Perkin Trans. 1 1980 11
6. Application of the Barton photochemical reaction in the synthesis of 1-dethia-3-aza-1-carba-2-oxacephem: a novel agent against resistant pathogenic microorganisms
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7. Adducts from acyl chlorides and 2-unsubstituted oxazolines: formation and reactions
Bernard T. Golding,David R. Hall J. Chem. Soc. Perkin Trans. 1 1975 1302
8. The control of stereochemistry by the pentafluorosulfanyl group
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9. Key green chemistry research areas—a perspective from pharmaceutical manufacturers
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10. Further observations on the rearrangement of 3-acylaminoazetidinones
C. W. Bird,J. D. Twibell J. Chem. Soc. C 1971 3155