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Merck
CN

295949

1,4-二氧杂螺[4.5]-2-癸酮

95%

别名:

2,2-五亚甲基-1,3-二氧六环基-4-酮

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关于此项目

经验公式(希尔记法):
C8H12O3
化学文摘社编号:
分子量:
156.18
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Assay:
95%
Form:
solid
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assay

95%

form

solid

bp

70 °C/0.5 mmHg (lit.)

mp

32-35 °C (lit.)

SMILES string

O=C1COC2(CCCCC2)O1

InChI

1S/C8H12O3/c9-7-6-10-8(11-7)4-2-1-3-5-8/h1-6H2

InChI key

HBGAMCTZOLJGAS-UHFFFAOYSA-N

Application

1,4-Dioxaspiro[4.5]decan-2-one has been used in the synthesis of L-callipeltose, the deoxyamino sugar of L-callipeltoside A.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

221.0 °F - closed cup

flash_point_c

105 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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分析证书(COA)

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D A Evans et al.
Organic letters, 3(20), 3133-3136 (2001-09-28)
[reaction: see text] The L-callipeltose subunit of L-callipeltoside A has been synthesized in 10 steps and 13% overall yield from D-threonine. The key steps are a highly diastereoselective Felkin anti aldol addition to a methyl ketone and a selective methylation