60478-96-8 (6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-,6,8-Dioxabicyclo[3.2.1]octane, 1,5-dimethyl-)

快速询单

结构式：

6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-MOL文件

CAS号：

60478-96-8

中文名称：

6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-

英文名称：

6,8-Dioxabicyclo[3.2.1]octane, 1,5-dimethyl-

分子式：

C₈H₁₄O₂

分子量：

142.195562839508

6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-(60478-96-8)名称与标识符

名称

英文别名：

6,8-Dioxabicyclo[3.2.1]octane, 1,5-dimethyl-;1,5-Dimethyl-6,8-dioxabicyclo[3.2.1]octane;

标识符

InChIKey：

AZWKCIZRVUVZPX-UHFFFAOYSA-N

Inchi：

1S/C8H14O2/c1-7-4-3-5-8(2,10-7)9-6-7/h3-6H2,1-2H3

SMILES：

CC12OC(CCC1)(C)OC2

6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-(60478-96-8)物化性质

实验特性

PSA : 18.46

计算特性

精确分子量 : 142.09942

6,8-二氧杂环[3.2.1]辛烷，1,5-二甲基-(60478-96-8)相关文献

1. A facile synthesis of 5-methyl-6,8-dioxabicyclo[3.2.1]octan-3-ones from 4-(t-butyldimethylsiloxy)pent-3-en-2-one and protected α-ketols. A synthesis of (±)-frontalin
Hisahiro Hagiwara,Hisashi Uda J. Chem. Soc. Perkin Trans. 1 1985 283
2. Synthesis of one enantiomer, the other enantiomer, and a mixture of both enantiomers of frontalin from a derivative of methyl-α-D-glucopyranoside
David R. Hicks,Bert Fraser-Reid J. Chem. Soc. Chem. Commun. 1976 869
3. Total synthesis of (+)- and (–)-frontalin
Albert W. M. Lee J. Chem. Soc. Chem. Commun. 1984 578
4. Synthesis of (–)-frontalin from α-D-isosaccharino-1,4-lactone
Minh-Chau Trinh,Jean-Claude Florent,Claude Monneret J. Chem. Soc. Chem. Commun. 1987 615
5. A short synthesis of (R)-(+)-frontalin and Latia luciferin using new organosilicon reagents
Philip Magnus,Glenn Roy J. Chem. Soc. Chem. Commun. 1978 297
6. Synthesis of (–)-frontalin from the (2S,3R)-diol prepared from α-methylcinnamaldehyde and fermenting baker's yeast
Claudio Fuganti,Piero Grasselli,Stefano Servi J. Chem. Soc. Perkin Trans. 1 1983 241
7. Convenient synthetic route to 6,8-dioxabicyclo[3.2.1]octanes, the aggregation pheromone components of bark beetles
Navalkishore N. Joshi,Vasant R. Mamdapur,Mohindra S. Chadha J. Chem. Soc. Perkin Trans. 1 1983 2963
8. Asymmetric construction of α,α–disubstituted cyclobutanones–enantioselective total synthesis of (–)-frontalin
Hideo Nemoto,Toshie Yamada,Hiroki Ishibashi,Keiichiro Fukumoto J. Chem. Soc. Perkin Trans. 1 1991 3149
9. Volatiles from nineteen recently genome sequenced actinomycetes
Christian A. Citron,Lena Barra,Joachim Wink,Jeroen S. Dickschat Org. Biomol. Chem. 2015 13 2673
10. The Kulinkovich hydroxycyclopropanation reaction in natural product synthesis
Isabell Haym,Margaret A. Brimble Org. Biomol. Chem. 2012 10 7649

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