50967-93-6 (L-青霉胺盐酸盐一水合物,Hydrochlorid-hydrat DL-penicillaminat)

快速询单

结构式：

L-青霉胺盐酸盐一水合物MOL文件

CAS号：

50967-93-6

中文名称：

L-青霉胺盐酸盐一水合物

英文名称：

Hydrochlorid-hydrat DL-penicillaminat

分子式：

C₅H₁₄ClNO₃S

分子量：

203.6876

L-青霉胺盐酸盐一水合物(50967-93-6)名称与标识符

名称

英文别名：

H-Pen-OH HCl H2O;hydrochlorid-hydrat dl-penicillaminat;2-Amino-3-mercapto-3-methylbutanoic acid hydrochloride hydrate;(+)-penicillamine hydrochloride;50967-93-6;NS00083768;Penicillamine DL-form hydrochloride;(R)-2-Amino-3-mercapto-3-methylbutanoic acid hydrochloride;NS00085721;Q27283296;(2R)-2-amino-3-methyl-3-sulfanylbutanoic acid hydrochloride;L-VALINE, 3-MERCAPTO-, HYDROCHLORIDE (1:1);3-Mercapto-L-valine hydrochloride;3-Mercapto-L-valine HCl;NSC-81988;(R)-2-Amino-3-mercapto-3-methylbutanoicacidhydrochloride;SCHEMBL316497;L-Penicillamine hydrochloride;NSC 81988;3-Mercapto-L-valine Hydrochloride; L-Penicillamine Hydrochloride; NSC 81988; (R)-2-Amino-3-mercapto-3-methylbutanoic Acid Hydrochloride;UNII-M06MU5T9DS;DTXSID30177097;EINECS 247-077-9;H-Pen-OHHClH2O;CZDHUFYOXKHLME-AENDTGMFSA-N;25526-04-9;(2R)-2-Amino-3-methyl-3-sulfanylbutanoic Acid HCl;E87319;Penicillamine hydrochloride, (+)-;(2R)-2-amino-3-methyl-3-sulfanylbutanoic acid;hydrochloride;EN300-7648176;M06MU5T9DS;

标识符

InChIKey：

FSSISUZJDVXKOS-UHFFFAOYSA-N

Inchi：

1S/C5H11NO2S.ClH.H2O/c1-5(2,9)3(6)4(7)8;;/h3,9H,6H2,1-2H3,(H,7,8);1H;1H2

SMILES：

Cl[H].S([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])(C(=O)O[H])N([H])[H].O([H])[H]

L-青霉胺盐酸盐一水合物(50967-93-6)物化性质

计算特性

精确分子量 : 185.0277275g/mol
氢键供体数量 : 5
氢键受体数量 : 5
可旋转化学键数量 : 2
同位素质量 : 185.0277275g/mol
重原子数量 : 11
复杂度 : 124
同位素原子数量 : 0
确定原子立构中心数量 : 1
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 : 2
拓扑分子极性表面积 : 65.3

L-青霉胺盐酸盐一水合物(50967-93-6)推荐厂家更多厂家(2)

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金锦乐（湖南）化学有限公司		金锦乐	1226360695		询单
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L-青霉胺盐酸盐一水合物(50967-93-6)相关文献

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3. Gold complexes of L-cysteine and D-penicillamine
Donald H. Brown,Gordon C. McKinley,W. Ewen Smith J. Chem. Soc. Dalton Trans. 1978 199
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Paul A. Cusack,Peter J. Smith,John D. Donaldson J. Chem. Soc. Dalton Trans. 1982 439
8. 676. Syntheses in the penicillin field. Part V. The structure and reduction of some thiazolinyloxalones
R. Bentley,A. H. Cook,J. A. Elvidge J. Chem. Soc. 1949 3216
9. 856. Syntheses in the penicillin field. Part X. 4-Formylisooxazolones and derived thiazolidines
A. H. Cook,G. Shaw J. Chem. Soc. 1952 4466
10. 501. Syntheses in the pencillin field. Part IV. Some 2-substituted thiazolines and their reactivity
A. H. Cook,J. A. Elvidge,G. Shaw J. Chem. Soc. 1949 2367