10159-79-2 (八氢-2H-喹啉-1-甲醇,Octahydro-2H-quinolizin-1-yl-methanol)

快速询单

结构式：

八氢-2H-喹啉-1-甲醇MOL文件

CAS号：

10159-79-2

中文名称：

八氢-2H-喹啉-1-甲醇

英文名称：

Octahydro-2H-quinolizin-1-yl-methanol

分子式：

C₁₀H₁₉NO

分子量：

169.263962984085

八氢-2H-喹啉-1-甲醇(10159-79-2)名称与标识符

名称

中文别名：

八氢-2H-喹啉-1-甲醇;

英文别名：

2H-Quinolizine-1-methanol,octahydro-;2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethanol;LUPININE;(+-)-Epilupinin;(1R,9aR)-1-(Octahydroquinolizin-1-yl)methanol;< 14C> -Lupinin;1-Epilupinine;1-Hydroxymethylchinalisidin;2H-Quinolizine-1-methanol, octahydro-, (1R-trans)-;2H-Quinolizine-1-methanol, octahydro-, (1S-cis)-;AC1L6RDW;DL-1-Epilupinin;Maybridge1_002482;octahydroquinolizin-1-yl-methanol;SureCN914675;UPCMLD-DP047;(OCTAHYDRO-QUINOLIZIN-1-YL)-METHANOL;OCTAHYDRO-2H-QUINOLIZIN-1-YLMETHANOL;(octahydro-1H-quinolizin-1-yl)methanol;1-(Hydroxymethyl)octahydro-2H-quinolizine;Lupinine, (Octahydro-2H-quinolizin-1-yl)methanol;CCG-47843;10248-30-3;(hydroxymethyl)octahydro quinolizine;SR-01000637434-4;F0451-0451;SCHEMBL914675;NSC-168348;NCGC00095325-03;BB 0260512;HMS548I18;octahydro-1H-quinolizin-1-ylmethanol;FT-0636646;1212428-68-6;SB45319;2H-Quinolizine-1-methanol, octahydro-;SR-01000637434;NCGC00095325-01;DTXSID80871679;MFCD00017327;AKOS015840860;SR-01000637434-1;10159-79-2;FT-0604398;CERAPP_61140;EN300-114803;NCGC00095325-04;(Octahydro-2H-quinolizin-1-yl)methanol;SDCCGMLS-0065897.P001;NSC168348;PS-3068;CDS1_000194;Octahydro-2H-quinolizin-1-ylmethanol #;DTXSID10304925;SR-01000637434-3;2-(NAPHTHALEN-1-YLAMINO)-BENZOICACID;UPCMLD-DP047:001;DivK1c_001234;HDVAWXXJVMJBAR-UHFFFAOYSA-N;

标识符

MDL：

MFCD00017327

InChIKey：

HDVAWXXJVMJBAR-UHFFFAOYSA-N

Inchi：

1S/C10H19NO/c12-8-9-4-3-7-11-6-2-1-5-10(9)11/h9-10,12H,1-8H2

SMILES：

OCC1CCCN2CCCCC21

八氢-2H-喹啉-1-甲醇(10159-79-2)物化性质

实验特性

LogP : 1.18110
PSA : 23.47
折射率 : 1.525
沸点 : 269-270°C
熔点 : 68-70°C
闪点 : 99.1 °C
密度 : 1.04

计算特性

精确分子量 : 169.14677
氢键供体数量 : 1
氢键受体数量 : 2
可旋转化学键数量 : 1
同位素质量 : 169.147
重原子数量 : 12
复杂度 : 149
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 : 2
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） : 1.2
拓扑分子极性表面积 : 23.5Å²

八氢-2H-喹啉-1-甲醇(10159-79-2)安全信息

安全术语： S23-36/37/39
安全说明： 23-36/37/39
风险术语： R23/24/25
危险品标志： Xi
危险品运输编号： UN 1544
危险类别码： 23/24/25
HazardClass： IRRITANT

八氢-2H-喹啉-1-甲醇(10159-79-2)推荐厂家更多厂家(3)

公司名称	手机号/电话	联系人	QQ	询单
湖北扬信医药科技有限公司	18071854684 0714-3999001	程舒畅	2885409691	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695	询单
江苏艾康生物医药研发有限公司	18795912720 025-66061636	杨情情	3004779232	询单

八氢-2H-喹啉-1-甲醇(10159-79-2)相关文献

1. Application of the aza-Diels–Alder reaction in the synthesis of natural products
Min-Hui Cao,Nicholas J. Green,Sheng-Zhen Xu Org. Biomol. Chem. 2017 15 3105
2. Complementary enantioselective approaches to the quinolizidine alkaloids lupinine and epilupinine by enolate Claisen rearrangements or direct allylation of piperidin-2-ylacetic acid derivatives
Christopher Morley,David W. Knight,Andrew C. Share J. Chem. Soc. Perkin Trans. 1 1994 2903
3. Application of 13C n.m.r. spectroscopy to study the biosynthesis of the quinolizidine alkaloids lupinine and sparteine
Jatinder Rana,David J. Robins J. Chem. Soc. Perkin Trans. 1 1986 1133
4. An efficient asymmetric synthesis of (?)-lupinine
Stephen G. Davies,Ai M. Fletcher,Emma M. Foster,Ian T. T. Houlsby,Paul M. Roberts,Thomas M. Schofield,James E. Thomson Chem. Commun. 2014 50 8309
5. Application of 2H n.m.r. spectroscopy to study the incorporation of enantiomeric 2H-labelled cadaverines into quinolizidine alkaloids
Alison M. Fraser,David J. Robins J. Chem. Soc. Perkin Trans. 1 1987 105
6. The asymmetric syntheses of pyrrolizidines, indolizidines and quinolizidines via two sequential tandem ring-closure/N-debenzylation processes
Stephen G. Davies,Ai M. Fletcher,Emma M. Foster,Ian T. T. Houlsby,Paul M. Roberts,Thomas M. Schofield,James E. Thomson Org. Biomol. Chem. 2014 12 9223
7. Biosynthesis of quinolizidine alkaloids in lupins: mechanistic considerations and prospects for pathway elucidation
Davide Mancinotti,Karen Michiko Frick,Fernando Geu-Flores Nat. Prod. Rep. 2022 39 1423
8. Quinolizidine alkaloid biosynthesis: incorporation of [1-amino-15N, 1-13C]cadaverine into lupinine
Jatinder Rana,David J. Robins J. Chem. Soc. Chem. Commun. 1984 81
9. Stereochemistry of quinolizidine alkaloid biosynthesis: incorporation of the enantiomeric [2-2H]cadaverines into lupinine
David J. Robins,Gary N. Sheldrake J. Chem. Soc. Chem. Commun. 1994 1331
10. A 13C n.m.r. study of the biosynthesis of lupinine and sparteine
W. Marek Golebiewski,Ian D. Spenser J. Chem. Soc. Chem. Commun. 1983 1509